NZ732015B2 - Anti-EGFR antibody drug conjugate formulations - Google Patents

Abstract

Discloses anti-EGFR antibody-auristating drug conjugate formulations comprising an IgG antibody. The antibody has the HCDR sequences of SEQ ID NO: 15-17 and the LCDRs of SEQ ID NO: 20-22 or the HCVR of SEQ ID NO: 13 and the LCVR of SEQ ID NO: 18. The auristatin can be monomethylauristatin F (MMAF). The formulation further comprises a sugar, buffer and a surfactant, wherein the buffer is selected from the group consisting of acetate, succinate, gluconate, methionine, imidazole, histidine, glycine, arginine, citrate, phosphate, and citrate and phosphate The formulation further comprises a sugar, buffer and a surfactant, wherein the buffer is selected from the group consisting of acetate, succinate, gluconate, methionine, imidazole, histidine, glycine, arginine, citrate, phosphate, and citrate and phosphate

Description

ANTI-EGFR ANTIBODY DRUG CONJUGATE FORMULATIONS RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. 61/790,490, filed on March 15, 2013. The contents of the aforementioned ty document are hereby incorporated by reference in its entirety.

The present application is a divisional application of New Zealand Patent Application No. 630826 (), the content of which is incorporated herein by reference in its entirety.

INTRODUCTION Human epidermal growth factor receptor (also known as HER-1 or Erb-B1, and referred to herein as "EGFR") is a 170 kDa transmembrane receptor encoded by the c-erbB ncogene, and ts intrinsic tyrosine kinase activity (Modjtahedi et al., Br. J. Cancer 73:228-235 (1996); Herbst and Shin, Cancer 3-1611 ). SwissProt se entry P00533 provides the sequence of EGFR. EGFR tes numerous cellular processes via tyrosine-kinase mediated signal transduction pathways, ing, but not limited to, activation of signal uction pathways that control cell proliferation, differentiation, cell al, sis, angiogenesis, mitogenesis, and metastasis (Atalay et al., Ann. Oncology 14:1346-1363 (2003); Tsao and Herbst, Signal 4:4-9 (2003); Herbst and Shin, Cancer 94:1593-1611 (2002); Modjtahedi et al., Br. J. Cancer 73:228-235 (1996)).

Overexpression of EGFR has been reported in numerous human malignant ions, including cancers of the bladder, brain, head and neck, pancreas, lung, breast, ovary, colon, prostate, and kidney (Atalay et al., Ann. Oncology 14:1346-1363 (2003); Herbst and Shin, Cancer 94:1593- 1611 (2002) Modjtahedi et al., Br. J. Cancer 73:228-235 (1996)). In many of these conditions, the overexpression of EGFR correlates or is associated with poor prognosis of the patients (Herbst and Shin, Cancer 94:1593-1611 (2002) Modjtahedi et al., Br. J. Cancer 73:228-235 (1996)). EGFR is also expressed in the cells of normal tissues, particularly the epithelial tissues of the skin, liver, and gastrointestinal tract, although at generally lower levels than in malignant cells (Herbst and Shin, Cancer 94:1593-1611 (2002)).

A significant proportion of tumors containing amplifications of the EGFR gene (i.e., multiple copies of the EGFR gene) also co-express a truncated version of the receptor (Wikstrand et al. (1998) J. irol. 4, 148-158) known as de2-7 EGFR, ΔEGFR, or Δ2-7 (terms used hangeably herein) (Olapade-Olaopa et al. (2000) Br. J. . 82, 186-94). The rearrangement seen in the de2-7 EGFR results in an in-frame mature mRNA lacking 801 nucleotides spanning exons 2-7 (Wong et al. (1992) Proc. Natl. Acad. Sci. U.S.A. 89, 2965-9; Yamazaki et al. (1990) Jpn. J. Cancer Res. 81, 773-9; Yamazaki et al. (1988) Mol. Cell. Biol. 8, 1816-20; Sugawa et al. (1990) Proc. Natl. Acad. Sci. U.S.A. 87, 8602-6). The corresponding EGFR n has a 267 amino acid deletion comprising residues 6-273 of the extracellular domain and a novel glycine residue at the fusion junction (Sugawa et al., 1990).

This deletion, together with the insertion of a glycine residue, produces a unique junctional peptide at the deletion interface (Sugawa et al., 1990).

The de2-7 EGFR has been reported in a number of tumor types including glioma, breast, lung, ovarian and prostate (Wikstrand et al. (1997) Cancer Res. 57, 4130-40; Olapade- Olaopa et al. (2000) Br. J. Cancer. 82, 186-94; and, et al. (1995) Cancer Res. 55, 3140- 8; Garcia de o et al. (1993) Cancer Res. 53, 3217-20). While this truncated receptor does not bind ligand, it possesses low constitutive activity and imparts a significant growth advantage to glioma cells grown as tumor xenografts in nude mice (Nishikawa et al. (1994) Proc. Natl. Acad. Sci. U.S.A. 91, 1) and is able to transform NIH3T3 cells (Batra et al. (1995) Cell Growth Differ. 6, 1251-9) and MCF-7 cells. The cellular mechanisms utilized by the de2-7 EGFR in glioma cells are not fully d but are reported to include a decrease in apoptosis (Nagane et al. (1996) Cancer Res. 56, 5079-86) and a small enhancement of eration (Nagane et al., 1996).

As expression of this truncated receptor is restricted to tumor cells it represents a highly specific target for antibody therapy. Accordingly, there is a need in the art for anti- EGFR antibodies and formulations that can e ive treatment to those in need thereof.

Antibody drug conjugates (ADC) ent a new class of therapeutics comprising an antibody conjugated to a cytotoxic drug via a chemical linker. A number of ADCs are being tested in clinical trials today, including trastuzumab (Herceptin (anti-HER2 antibody) linked to DM1; Genentech / Roche) and glembatumumab vedotin (CDX-011; an anti-GPNMB antibody linked to MMAE; Celldex Therapeutics). The eutic concept of ADCs is to use an antibody as a e to deliver a cytotoxic drug to a tumor cell by means of binding to a target surface antigen. ADCs have more complex and heterogeneous ures than the unconjugated antibodies. Accordingly, ADCs present a challenge for formulating for therapeutic purposes.

Summary of Invention The present invention provides formulations comprising antibody-drug conjugates (ADCs) and s relating to the use of such ates to treat disorders requiring treatment with an anti-epidermal growth factor receptor (anti-EGFR) ADC, such as cancer.

In a first aspect there is provided a lyophilized formulation comprising an anti-Epidermal Growth Factor or (EGFR) antibody drug conjugate (ADC), a sugar, a buffer, and a surfactant, wherein said formulation has a pH of about 5 – 7 upon reconstitution, wherein said anti-EGFR ADC comprises an anti-EGFR antibody conjugated to an auristatin, wherein the antibody is an IgG dy comprising a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid ces set forth in SEQ ID NOS: 15, 16, and 17, and comprising a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22 and wherein the buffer is selected from the group consisting of acetate, succinate, gluconate, methionine, imidazole, histidine, glycine, arginine, citrate, phosphate, and citrate and phosphate.

In a second aspect there is provided the use of the formulation according to the first aspect, in the manufacture of a medicament for ng cancer.

The invention provides a formulation comprising an anti-Epidermal Growth Factor Receptor (EGFR) antibody drug conjugate (ADC), a sugar, histidine, and a surfactant, n the formulation has a pH of about 5 - 7, and n the anti-EGFR ADC comprises an anti- EGFR antibody, or antigen-binding portion thereof, conjugated to an auristatin.

The ion provides a formulation comprising an anti-Epidermal Growth Factor Receptor (EGFR) antibody drug conjugate (ADC), a sugar, a succinate or citrate and/or phosphate buffer, and a surfactant, wherein the formulation has a pH of about 5 - 7, and wherein the anti-EGFR ADC comprises an anti-EGFR antibody, or n-binding portion thereof, conjugated to an atin. In one embodiment, the formulation is lyophilized.

In one embodiment, the formulation comprises a surfactant which is a rbate, e.g., polysorbate 80, or a poloxamer. In one ment, the formulation comprises 0.05-0.15 mg/ml of a polysorbate.

In another embodiment, the formulation comprises about 60-80 mg/ml of a sugar. In one ment, the sugar is selected from the group ting of mannitol, sorbitol, sucrose, and trehalose.

In one embodiment, the formulation of the invention comprises about 5-25 mM ine.

In another further embodiment, the formulation is lyophilized. In one embodiment, the formulation is lyophilized and the sugar is sucrose. In another embodiment of the invention, the lyophilized formulation does not comprise lactobionic acid. In r embodiment of the invention, the lyophilized formulation does not comprise a sugar acid.

In one embodiment, the formulation of the invention is aqueous, and comprises about 1-40 mg/ml of an anti-EGFR ADC.

In a further embodiment, the formulation of the invention comprises 1-150 mg of the anti- EGFR ADC. In one embodiment, the ation of the invention comprises 90-110 mg of an anti-EGFR ADC.

In one embodiment, the formulation of the invention has a pH of about 5 to 7. In a further embodiment, the formulation has a pH of about 5.5 to 6.5.

In one embodiment, the auristatin is thylauristatin F (MMAF). In one embodiment, the formulation of the invention ses an anti-EGFR ADC comprising an anti-EGFR antibody, or antigen-binding portion thereof, conjugated to Monomethylauristatin F (MMAF). In another embodiment, the MMAF is conjugated to the antibody with a maleimidocaproyl linker.

The invention r provides a lyophilized formulation comprising an anti- Epidermal Growth Factor Receptor (EGFR) antibody drug conjugate (ADC) comprising an GFR antibody, or antigen-binding portion thereof, conjugated to an auristatin, a sugar, e.g., sucrose, a surfactant, e.g., a polysorbate, such as polysorbate 80, and histidine. In one embodiment, the lyophilized formulation comprises 1-20 mg of histidine, about 0 mg of a sugar, about 0.1 to 0.9 mg of a surfactant, and about 1-150 mg of the anti-EGFR ADC.

The invention also provides an s formulation comprising about 1 - 100 mg/ml of an anti-Epidermal Growth Factor Receptor (EGFR) dy drug conjugate (ADC) sing an anti-EGFR antibody, or antigen-binding portion thereof, conjugated to an auristatin, about 1 -10 mg/mL histidine, about 50 -90 mg/ml of a sugar, e.g., e, and about 0.01 - 0.2 mg/ml of a surfactant, e.g., polysorbate 80.

In one ment, the formulation of the invention comprises an anti-EGFR ADC wherein the anti-EGFR antibody is humanized.

In another embodiment, the formulation of the invention comprises an anti-EGFR ADC wherein the anti-EGFR antibody comprises a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 13, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 18.

In another embodiment, the formulation of the invention comprises an anti-EGFR ADC wherein the anti-EGFR antibody comprises a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO: 13, a heavy chain constant region having the amino acid sequence as set forth in SEQ ID NO: 14, a light chain variable region having the amino acid sequence set forth in SEQ ID NO: 18, and a light chain constant region having the amino acid sequence as set forth in SEQ ID NO: 19, In a further embodiment, the ation of the invention ses an anti-EGFR ADC n the antibody comprises a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid sequences set forth in SEQ ID NOS: 15, 16, and 17, and comprises a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22.

In another embodiment of the invention, the anti-EGFR ADC comprises CDRs (i.e., light chain CDR1, CDR2, and CDR3) described in the light chain variable region set forth in the amino acid sequence of SEQ ID NO: 18, and CDRs (i.e., heavy chain CDR1, CDR2, and CDR3) described in the amino acid ce of SEQ ID NO: 13.

The ion further provides a lyophilized ation comprising e, polysorbate 80, and histidine, and wherein the antibody comprises a heavy chain le region comprising complementarity domain regions (CDRs) comprising the amino acid sequences set forth in SEQ ID NOS: 15, 16, and 17, and comprises a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22. In one ment, the formulation comprises 1-110 mg of the anti-EGFR In one embodiment, the formulation of the invention contains an ADC mixture comprising GFR ADCs having an average DAR of about 3 or an ADC mixture comprising anti-EGFR ADCs having a DAR of about 2-4.

In one embodiment, the formulation of the ion comprises an anti-EGFR ADC sing an anti-EGFR antibody, or antigen-binding portion thereof, conjugated to monomethyl auristatin F (MMAF), wherein said ADC 1-MMAF comprises a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid sequences set forth in SEQ ID NOS: 15, 16, and 17, and comprises a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22, e, histidine, and polysorbate 80, wherein the formulation comprises an ADC mixture having an average DAR of about 3 or an ADC mixture having a DAR of about 2-4. In a further embodiment of the invention, the formulation is lyophilized. In yet a further invention, the anti-EGFR antibody is linked to MMAF via a maleimidocaproyl linker.

In still a further embodiment, the anti-EGFR antibody, or antigen-binding portion thereof, comprises a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 13, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 18.

In one embodiment, the formulation of the invention comprises an anti-EGFR ADC sing an anti-EGFR antibody, or antigen-binding portion thereof, conjugated to monomethyl auristatin E (MMAE), wherein said ADC 1-MMAE comprises a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid sequences set forth in SEQ ID NOS: 15, 16, and 17, and comprises a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22, sucrose, histidine, and polysorbate 80, wherein the formulation comprises an ADC mixture having an average DAR of about 3 or an ADC mixture having a DAR of about 2-4. In a r embodiment of the invention, the ation is lyophilized. In still a further embodiment, the anti-EGFR antibody, or antigen-binding portion thereof, ses a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 13, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 18.

In one embodiment, the formulation of the invention is a pharmaceutical formulation.

The ion also features a method of preparing a formulation, wherein the method comprises lyophilizing an aqueous formulation having a pH ranging from about 5 to 7 and comprising 1-20 mg of ine, about 320-410 mg of the sugar, about 0.1 to 0.9 mg of the surfactant, and about 1-150 mg of the anti-EGFR ADC.

The invention further provides a method for treating a t comprising administering a therapeutically effective amount of an anti-EGFR ADC in the formulations described herein to a subject, wherein the subject has a disorder requiring treatment with the anti-EGFR ADC. In one embodiment, the disorder requiring treatment with the anti-EGFR ADC is cancer, e.g., glioblastoma, non-small cell lung cancer, lung cancer, colon cancer, head and neck cancer, breast cancer, squamous cell tumors, anal cancer, skin cancer, and vulvar .

In one embodiment, the formulation of the invention is used to treat solid tumors likely to over-express the Epidermal Growth Factor Receptor (EGFR) or squamous ll cell lung cancer (NSCLC).

In one embodiment, the ation of the invention is used to treat a cancer selected from the group consisting of squamous tumors (including, squamous tumors of the lung, head and neck, al, etc.), glioblastoma, glioma, non-small cell lung cancer, lung cancer, colon cancer, head and neck cancer, breast cancer, squamous cell tumors, anal cancer, skin cancer, and vulvar cancer.

In one embodiment, the ation of the ion is used to treat glioblastoma multiforme.

In one embodiment, the formulation of the invention is used to treat a solid tumor having overexpression of EGFR. In one ment, the ation of the invention is used to treat a subject having an advanced solid tumor likely to overexpress EGFR.

In one embodiment, the formulations of the invention are administered enously.

The invention also provides kits comprising the formulations bed herein.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a diagram that shows the structure of MMAE coupled to an antibody of interest (mAb) by a linker (GN Linkers + Auristatin: vcMMAE).

Figure 2 is a diagram that shows the structure of MMAF d to an antibody of interest (mAb) by a linker (Linkers + Auristatin: mcMMAF).

Figure 3 (A and B) graphically depict the onset of unfolding temperature as determined with c scanning fluorescence (A) and differential ng calorimetry (B). ♦ antibody 1; ■ Antibody Drug Conjugate (ADC) 1- MMAF; ▲ ADC 1- MMAE.

Figure 4 (A and B) graphically depicts the presence of unstructured elements in antibody 1, ADC 1- MMAF and ADC 1- MMAE using Fourier Transform Infrared Spectroscopy (FTIR) (A) and near UV- Circular Dichroism (CD) (B). ♦ antibody 1; ■ ADC 1- MMAF; ▲ ADC 1- MMAE.

Figure 5 graphically depicts the aggregation propensity of ADC 1- MMAE at low concentrations, compared to ADC 1- MMAF and antibody 1.

Figure 6 graphically depicts the aggregation propensity of ADC 1- MMAE at high concentrations, compared to ADC 1- MMAF and antibody 1.

Figure 7 shows a schematic of the serum stability assay, and describes the in vitro serum stability of a number of molecules, including antibody 1, the ADC 1- MMAF and ADC 1- MMAE.

Figure 8 (A and B) graphically depicts freeze/thaw stability, indicated by percentage of monomer present, as determined by SEC among antibody 1, ADC 1- MMAF and ADC 1- MMAE formulations in 15 mM histidine buffer at pH 5.75 (A) and 1 mg/ml pH 7.0 10 mM citrate and 10 mM phosphate buffer.

Figure 9 (A and B) is a graph quantifying subvisible particle formation during freeze- thawing as determined by microflow imaging (MFI).

DETAILED DESCRIPTION I. Definitions In order that the present invention may be more readily understood, certain terms are first defined. In addition, it should be noted that er a value or range of values of a parameter are recited, it is intended that values and ranges intermediate to the recited values are also ed to be part of this invention.

The terms "anti-Epidermal Growth Factor antibody drug conjugate" or "anti-EGFR antibody drug conjugate" and "anti-EGFR ADC", used hangeably herein, refer to an antibody-drug conjugate comprising an antibody that specifically binds to EGFR, whereby the antibody is conjugated to a drug, e.g., a cytotoxic agent such as an auristatin (e.g., monomethyl auristatin F). In one embodiment, the anti-EGFR antibody drug conjugate is the ADC 1-MMAF, which is antibody 1 conjugated to MMAF via a maleimidocaproyl (mc) linkage. Amino acid sequences corresponding to the light and heavy chains of antibody 1 are provided in SEQ ID NOs: 13 to 22. Unless otherwise specified, the term MMAF" as used herein in inclusive of purified MAF (also referred to as MAFp).

The term "auristatin", as used herein, refers to a family of antimitotic agents.

Auristatin derivatives are also included within the definition of the term "auristatin".

Examples of atins include, but are not limited to, auristatin E (AE), monomethyl auristatin E (MMAE), monomethyl atin F (MMAF), and synthetic analogs of atin.

The term EGFR antibody" is meant to refer to an antibody that specifically binds to EGFR. An antibody "which binds" an n of interest, i.e., EGFR, is one capable of binding that antigen with sufficient affinity such that the antibody is useful in targeting a cell expressing the antigen.

The term "ADC mixture," as used herein, refers to a composition containing a heterogeneous DAR distribution of ADCs. In one ment, an ADC mixture contains anti-EGFR ADCs having a distribution of DARs of 1 to 8, e.g., 2, 4, 6, and 8 (i.e., drug loaded species of 2, 4, 6, and 8). In another embodiment, an ADC mixture contains anti- EGFR ADCs having DARs of less than 4, e.g., a DAR of 2-4. Notably, degradation products may result such that DARs of 1, 3, 5, and 7 may also be included in the mixture. Further, ADCs within the mixture may also have DARs greater than 8. The ADC mixture results from interchain disulfide reduction followed by conjugation.

The term "ADC1-MMAFp", as used herein, refers to an ADC1-MMAF molecule that is found within an ADC mixture that has been purified such that the DAR of the ADC is within a desired range, e.g., (a DAR of 2-4) or the ADC is included in an ADC mixture having a desired average, (e.g., an average DAR of 3).

The term "formulation" as used herein is meant to refer to an aqueous formulation or a lyophilized formulation. In one embodiment, the formulation of the invention is lyophilized. In one embodiment, the formulation of the invention is aqueous. In one embodiment, the formulation of the invention does not include a chelator. In one embodiment, the lyophilized formulation of the ion does not include a chelator.

The term "aqueous formulation" refers to a solution in which the t is water. In one embodiment, the term "aqueous ation" refers to a liquid formulation in which the solvent is water n the formulation was not previously lyophilized, (i.e., does not result from reconstitution of a lyophilized formulation). In another ment, the term "aqueous formulation" refers to a liquid formulation in which the t is water wherein the formulation was previously lyophilized (i.e., a reconstituted formulation).

The term "lyophilized" as used herein in connection with the formulation according to the invention denotes a formulation which is dried by freezing the formulation and subsequently subliming the ice from the frozen content by any freeze-drying methods known in the art, for example commercially available freeze-drying devices.

A "reconstituted" formulation is one which has been prepared by dissolving a lyophilized formulation containing a protein, e.g., an ADC, in a t such that the protein is dispersed in the tituted formulation. The tituted formulation is suitable for administration (e.g. enous administration) to a t to be treated with the protein of interest (e.g., anti-EGFR antibody drug conjugate).

A "diluent" of interest herein is one which is pharmaceutically acceptable (safe and xic for administration to a human) and is useful for the preparation of a liquid formulation, such as a formulation reconstituted after lyophilization. Exemplary diluents include sterile water, bacteriostatic water for ion (BWFI), a pH buffered solution (e.g. phosphate-buffered saline), sterile saline solution, Ringer's solution or dextrose solution. In an alternative embodiment, diluents can include s solutions of salts and/or buffers.

The term "buffer" refers to a compound that resists changes in pH by the action of its acid-base conjugate ents when in solution. In one embodiment, a buffer used in this invention has a pH in the range from about 4.5 to about 7.5. Examples of buffers that will control the pH in this range include acetate (e.g., sodium acetate), succinate (such as sodium succinate), gluconate, methionine, imidazole, histidine, glycine, arginine, citrate, phosphate, citrate and phosphate, Tris, and other organic acid s. In one embodiment, the buffer used in the formulation comprises ine, succinate, or citrate or phosphate buffer. In one embodiment of the invention, the formulation ses about 1 -10 mg/mL of a buffer comprising histidine. In another embodiment of the invention, the formulation ses 1- mg of a buffer comprising histidine.

The term "sugar" is meant to refer to as used herein denotes a monosaccharide or an oligosaccharide. A monosaccharide is a monomeric ydrate which is not hydrolysable by acids, ing simple sugars and their derivatives, e.g. aminosugars. es of ccharides include, but are not limited to, glucose, fructose, galactose, mannose, sorbose, ribose, deoxyribose, neuraminic acid. An oligosaccharide is a carbohydrate consisting of more than one monomeric saccharide unit connected via glycosidic bond(s) either branched or in a chain. The monomeric saccharide units within an oligosaccharide can be identical or different. Depending on the number of monomeric saccharide units the oligosaccharide is a di-, tri-, tetra-, penta- and so forth saccharide. Examples of oligosaccharides include, but are not limited to, maltose, sucrose, lactose, melezitose, trehalose, sorbose, and ose. In contrast to polysaccharides, monosaccharides and oligosaccharides are water soluble. es of sugars include, but not limited to, a reducing sugar, a nonreducing sugar, a sugar alcohol, and a sugar acid. A ing sugar" is a sugar that contains a free aldehyde or ketone group and can reduce metal ions or react covalently with lysine and other amino groups in proteins. A ducing sugar" is a sugar that lacks a free aldehyde or ketonic group and is not oxidized by mild oxidizing agents such as Fehling’s or Benedict’s solutions. Examples of ng sugars are fructose, mannose, maltose, lactose, arabinose, xylose, , rhamnose, galactose and glucose. Nonreducing sugars include sucrose, trehalose, sorbose, melezitose and raffinose. Mannitol, xylitol, erythritol, threitol, sorbitol and glycerol are es of sugar alcohols. In one embodiment of the invention, the sugar is mannitol, sorbitol, sucrose, or trehalose. In another embodiment of the invention, the formulation comprises about 50 -90 mg/ml of a sugar, e.g., sucrose. In another further embodiment of the invention, the formulation comprises about 60-80 mg/ml of a sugar, e.g., sucrose. In another further embodiment of the invention, the formulation comprises about 70 mg/ml of a sugar, e.g., sucrose. In still another r embodiment of the invention, the lyophilized formulation comprises about 0 mg of a sugar.

The term "surfactant" generally refers to organic substances having amphipathic structures; namely, they are composed of groups of opposing solubility tendencies, typically an oil-soluble hydrocarbon chain and a water-soluble ionic group. Surfactants can be classified, depending on the charge of the surface-active moiety, into c, ic, and nonionic surfactants. Surfactants are often used as wetting, emulsifying, solubilizing, and dispersing agents for various pharmaceutical compositions and ations of biological materials. Examples of suitable surfactants include, but are not limited to, sodium lauryl sulfate, polysorbates such as polyoxyethylene an eate, monolaurate, monopalmitate, monstearate or another ester of polyoxyethylene an (e.g., the commercially available , such as, TWEEN 20 and TWEEN 80 (ICI Speciality Chemicals)), sodium dioctylsulfosuccinate (DOSS), lecithin, stearylic alcohol, cetostearylic alcohol, cholesterol, polyoxyethylene ricin oil, polyoxyethylene fatty acid glycerides, poloxamers (e.g., Pluronics F68TM and F108TM, which are block mers of ethylene oxide and propylene oxide); yethylene castor oil derivatives or mixtures thereof.

The term "polysorbate" as used herein refers to oleate esters of sorbitol and its anhydrides, typically copolymerized with ethylene oxide. In one ment, the polysorbate has a molecular weight g from about 1200 Da (approximate molecular weight of polysorbate 20) to about 1350 Da (approximate molecular weight of polysorbate 80). In one embodiment, a formulation comprises polysorbate 20, polysorbate 40, rbate 60, or polysorbate 80. In one embodiment, the formulation comprises about 0.1 to 0.9 mg of a polysorbate. In another embodiment, the formulation comprises about 0.01 - 0.2 mg/ml of a polysorbate. In another embodiment, the formulation comprises 0.05-0.15 mg/ml of a polysorbate.

The term "pharmaceutical formulation" refers to preparations that are in such a form as to permit the biological activity of the active ingredient(s) to be effective and, therefore, may be administered to a subject for therapeutic use.

A "stable" formulation is one in which the anti-EGFR antibody drug conjugate essentially retains its al ity and/or chemical stability and/or biological activity upon storage. Various ical techniques for measuring protein ity are available in the art and are reviewed in, e.g., Peptide and Protein Drug Delivery, pp. 247-301, Vincent Lee Ed., Marcel Dekker, Inc., New York, N.Y., Pubs. (1991) and Jones (1993) Adv. Drug Delivery Rev. 10: 29-90. In one embodiment, the stability of the anti-EGFR antibody drug conjugate is determined ing to the percentage of monomer protein in the solution, with a low percentage of degraded (e.g., fragmented) and/or aggregated n. For example, a formulation comprising a stable anti-EGFR antibody drug conjugate may include at least 95% monomer anti-EGFR dy drug conjugate. Alternatively, a formulation may include no more than 5% aggregate and/or degraded anti-EGFR antibody drug conjugate.

An anti-EGFR antibody drug conjugate "retains its physical stability" in a pharmaceutical formulation if it shows substantially no signs of aggregation, precipitation and/or denaturation upon visual examination of color and/or clarity, or as measured by UV light scattering or by size exclusion chromatography. In one embodiment, a stable aqueous formulation is a formulation having less than about 5% anti-EGFR antibody drug conjugate aggregation in the formulation.

An GFR antibody drug conjugate "retains its chemical ity" in a pharmaceutical formulation if the al stability at a given time is such that the anti- EGFR antibody drug conjugate is considered to still retain its ical activity as defined below. Chemical stability can be assessed by detecting and quantifying chemically altered forms of the anti-EGFR antibody drug conjugate. Chemical alteration may involve size modifications (e.g., clipping) which can be evaluated using size exclusion chromatography, SDS-PAGE and/or matrix-assisted laser desorption ionization / time of flight mass spectrometry /TOF MS), for example. Other types of chemical alternation include charge alteration (e.g., occurring as a result of deamidation), which can be evaluated by, e.g., change chromatography.

An anti-EGFR antibody drug conjugate "retains its biological ty" in a pharmaceutical formulation, if the protein in a pharmaceutical formulation is biologically active for its intended purpose. For example, biological ty of an anti-EGFR antibody drug conjugate is retained if the ical activity of the anti-EGFR antibody drug conjugate in the pharmaceutical formulation is within about 30%, about 20%, or about 10% (within the errors of the assay) of the biological activity exhibited at the time the pharmaceutical formulation was prepared (e.g., as determined in an antigen binding assay). In one embodiment, the biological activity is cytotoxicity of epidermoid carcinoma cells.

The term "antibody" broadly refers to an immunoglobulin (Ig) molecule, generally comprised of four polypeptide chains, two heavy (H) chains and two light (L) chains, or any functional fragment, , variant, or derivative thereof, that retains the essential target binding features of an Ig molecule.

In a full-length antibody, each heavy chain is comprised of a heavy chain variable region (abbreviated herein as HCVR or VH) and a heavy chain constant region. The heavy chain constant region is comprised of three s, CH1, CH2 and CH3. Each light chain is comprised of a light chain variable region viated herein as LCVR or VL) and a light chain constant region. The light chain constant region is sed of one domain, CL. The VH and VL regions can be further subdivided into regions of hypervariability, termed mentarity determining regions (CDR), interspersed with regions that are more conserved, termed framework s (FR). Each VH and VL is composed of three CDRs and four FRs, arranged from amino-terminus to y-terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4. Immunoglobulin molecules can be of any type (e.g., IgG, IgE, IgM, IgD, IgA and IgY) and class (e.g., IgG1, IgG2, IgG 3, IgG4, IgA1 and IgA2) or subclass.

The term "antigen-binding portion" of an antibody (or simply "antibody portion"), as used herein, refers to one or more fragments of an dy that retain the ability to specifically bind to an antigen (e.g., hIL-13). It has been shown that the antigen-binding function of an antibody can be performed by fragments of a full-length antibody. Such antibody embodiments may also be bispecific, dual specific, or multi-specific formats; ically binding to two or more different antigens. Examples of g fragments encompassed within the term "antigen-binding portion" of an dy include (i) a Fab fragment, a monovalent fragment consisting of the VL, VH, CL and CH1 domains; (ii) a F(ab')2 fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region; (iii) a Fd fragment consisting of the VH and CH1 domains; (iv) a Fv fragment consisting of the VL and VH domains of a single arm of an antibody, (v) a dAb fragment (Ward et al., (1989) Nature 341:544-546, Winter et al., PCT publication WO 90/05144 A1 herein incorporated by reference), which comprises a single variable domain; and (vi) an isolated complementarity determining region (CDR). rmore, although the two domains of the Fv fragment, VL and VH, are coded for by te genes, they can be joined, using recombinant methods, by a synthetic linker that enables them to be made as a single protein chain in which the VL and VH regions pair to form monovalent molecules (known as single chain Fv ; see e.g., Bird et al. (1988) e 242:423-426; and Huston et al. (1988) Proc. Natl. Acad. Sci. USA 85:5879-5883). Such single chain antibodies are also intended to be encompassed within the term "antigen-binding portion" of an dy. Other forms of single chain antibodies, such as diabodies are also encompassed.

Diabodies are bivalent, bispecific antibodies in which VH and VL domains are expressed on a single polypeptide chain, but using a linker that is too short to allow for pairing between the two domains on the same chain, thereby forcing the domains to pair with complementary domains of another chain and creating two antigen binding sites (see e.g., Holliger, P., et al. (1993) Proc. Natl. Acad. Sci. USA 90:6444-6448; Poljak, R.J., et al. (1994) Structure 2:1121- 1123). Such antibody binding portions are known in the art (Kontermann and Dubel eds., Antibody ering (2001) er-Verlag. New York. 790 pp. (ISBN 341354-5).

An ted antibody", as used herein, is intended to refer to an antibody that is substantially free of other dies having different antigenic specificities (e.g., an isolated antibody that specifically binds EGFR is substantially free of dies that specifically bind antigens other than EGFR). An isolated antibody that specifically binds EGFR may, however, have cross-reactivity to other antigens, such as EGFR molecules from other s.

Moreover, an isolated antibody may be substantially free of other cellular material and/or chemicals.

The term "humanized antibody" refers to antibodies which comprise heavy and light chain variable region sequences from a non-human species (e.g., a mouse) but in which at least a portion of the VH and/or VL sequence has been altered to be more "human-like", i.e., more similar to human germline variable sequences. In a particular embodiment, the term "humanized dy" refers to an antibody or dy variant, derivative or fragment, which specifically binds to an antigen of interest, and comprises a framework (FR) region having substantially the amino acid sequence of a human dy, and comprises CDRs having substantially the amino acid sequence of a non-human antibody. As used herein, the term "substantially" in the context of a CDR refers to a CDR having an amino acid sequence at least 80%, preferably at least 85%, at least 90%, at least 95%, at least 98% or at least 99% identical to the amino acid sequence of a non-human antibody CDR. In one embodiment, one type of humanized antibody is a CDR-grafted antibody, in which human CDR sequences are introduced into non-human VH and VL sequences to replace the corresponding nonhuman CDR sequences.

As used herein, the term "CDR" refers to the mentarity determining region within antibody le sequences. There are three CDRs in each of the variable regions of the heavy chain and the light chain, which are designated CDR1, CDR2 and CDR3, for each of the variable regions. The term "CDR set" as used herein refers to a group of three CDRs that occur in a single variable region capable of binding the antigen. The exact boundaries of these CDRs have been defined differently according to different systems. The system described by Kabat (Kabat et al., Sequences of Proteins of Immunological Interest (National Institutes of Health, Bethesda, Md. (1987) and (1991)) not only provides an guous residue numbering system applicable to any variable region of an antibody, but also provides precise residue boundaries defining the three CDRs. These CDRs may be referred to as Kabat CDRs. Chothia and ers (Chothia &Lesk, J. Mol. Biol. 196:901-917 (1987) and Chothia et al., Nature 342:877-883 ) found that certain sub- ns within Kabat CDRs adopt nearly identical peptide ne conformations, despite having great diversity at the level of amino acid sequence. These sub-portions were designated as L1, L2 and L3 or H1, H2 and H3 where the "L" and the "H" designates the light chain and the heavy chains regions, respectively. These regions may be referred to as Chothia CDRs, which have boundaries that overlap with Kabat CDRs. Other boundaries defining CDRs overlapping with the Kabat CDRs have been described by Padlan (FASEB J. 9:133-139 (1995)) and MacCallum (J Mol Biol 262(5):732-45 (1996)). Still other CDR boundary tions may not strictly follow one of the above systems, but will nonetheless overlap with the Kabat CDRs, although they may be shortened or lengthened in light of prediction or experimental findings that particular residues or groups of residues or even entire CDRs do not significantly impact n binding. The s used herein may utilize CDRs defined according to any of these systems, although preferred embodiments use Kabat or Chothia defined CDRs.

The term "disorder" refers to any condition that would benefit from treatment with the formulations of the invention, e.g., a disorder requiring treatment with the anti-EGFR dy in the formulation. This includes chronic and acute disorders or diseases including those pathological conditions that predispose the subject to the disorder in question.

The term "cancer" is meant to refer to or describe the physiological ion in mammals that is typically characterized by unregulated cell growth. Examples of cancer include, but are not limited to, carcinoma, lymphoma, blastoma, sarcoma, and leukemia or lymphoid malignancies. More particular examples of such cancers include glioblastoma, nonsmall cell lung cancer, lung cancer, colon , head and neck cancer, breast cancer, squamous cell tumors, anal cancer, skin cancer, and vulvar cancer. In one embodiment, the formulation is administered to a patient having a tumor(s) containing amplifications of the EGFR gene, whereby the tumor expresses the truncated version of the EGFR de2-7. In one embodiment, the formulation comprising ADC1-MMAF may be administered to a subject for the treatment of colorectal cancer, head and neck cancer (including, but not limited to, aryngeal , oropharyngeal cancer, esophageal cancer, laryngeal cancer, and oral cavity cancer), non-small cell lung cancer, pancreatic cancer, gastric cancer, breast cancer, a solid tumor, e.g., a solid tumor likely to xpress the Epidermal Growth Factor Receptor (EGFR), or glioblastoma multiforme.

The term "administering" as used herein is meant to refer to the delivery of a nce (e.g., an anti-EGFR antibody drug conjugate) to achieve a therapeutic objective (e.g., the treatment of an EGFR- associated disorder). Modes of stration may be parenteral, enteral and l. Parenteral administration is usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, eritoneal, transtracheal, aneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal and intrasternal injection and infusion.

The term "therapeutically effective amount" or "effective amount" of an ADC as used herein, refers to an amount ive in the prevention or treatment or alleviation of a symptom of a er for the treatment of which the ADC is effective.

The term "treatment" refers to both eutic treatment and lactic or preventative es. Those patients in need of treatment include those already with the disorder as well as those in which the disorder is to be prevented.

Various aspects of the invention are described in further detail in the following subsections.

II. Anti-EGFR Antibody Drug Conjugate Formulations of the Invention The present invention features ations comprising an anti-EGFR antibody, or an antigen-binding n thereof, wherein said EGFR antibody is conjugated to one or more drugs, e.g., an auristatin (e.g., MMAF). The present ion is based, at least in part, on the finding that a formulation comprising an anti-EGFR antibody drug conjugate (ADC), (wherein the anti-EGFR antibody, or antigen-binding portion thereof, is conjugated to one or more molecules of auristatin, such as MMAF), is able to maintain biological activity of the ADC upon reconstitution and maintain a drug to antibody ratio after reconstitution, following storage of the formulation for up to 6 months at 5°C and 25°C.

Formulations described herein may be lyophilized or aqueous. Unless otherwise indicated, the term lation" indicates both lyophilized and aqueous.

Certain formulations ably comprise an pidermal Growth Factor Receptor (EGFR) antibody drug conjugate (ADC), a sugar, a buffer, and a polysorbate, n the formulation has a pH of about 5 – 7. In certain embodiments, the formulation further comprises an anti-EGFR ADC comprising an anti-EGFR antibody, or antigen-binding portion thereof, such as antibody 1, which is conjugated to one or more molecules of an auristatin, such as MMAF.

In one embodiment, the invention provides a lyophilized formulation sing an anti-EGFR antibody drug conjugate, a sugar, e.g., sucrose, a surfactant, e.g., a rbate (such as polysorbate 80), and histidine, n the formulation has a pH of about 5 - 7, and wherein the anti-EGFR antibody drug conjugate comprises an anti-EGFR antibody, or antigen-binding portion thereof, conjugated to Monomethylauristatin F (MMAF).

In one embodiment, the invention provides a lyophilized formulation comprising an anti-EGFR antibody drug conjugate, sucrose, a surfactant, and a buffer, wherein the formulation has a pH of about 5 -7, and wherein the anti-EGFR antibody drug conjugate comprises an GFR antibody, or n-binding n thereof, e.g., antibody 1, conjugated via a maleimidocaproyl linker to Monomethylauristatin F (MMAF) (mc-MMAF).

In one embodiment, the invention provides a lyophilized formulation comprising an anti-EGFR antibody drug conjugate, sucrose, a rbate, and ine, wherein the formulation has a pH of about 5 - 7, and wherein the anti-EGFR antibody drug conjugate comprises an anti-EGFR antibody, or antigen-binding portion f, e.g., antibody 1, conjugated to via a maleimidocaproyl linker Monomethylauristatin F (MMAF) (mc-MMAF).

The formulations described herein preferably have a pH of about 4.0 to about 8.0. In one embodiment, the pH of the formulation ranges from about 5.0 to about 7.0; alternatively the pH may range from about 5 to about 6.5; alternatively the pH of the formulation may range from about 5.5 to about 6.5. The ranges intermediate to the entioned pH values, e.g., about 5.6 to about 6.4, are also intended to be part of the invention. Ranges of values using a combination of any of the aforementioned values as upper / lower limits are also intended to be included, e.g., a pH range of about 5.5 to about 6.2. ations of the invention preferably comprise an anti-EGFR ADC, a sugar, a surfactant, and a buffer. es of buffers known in the art that may be used in the formulations of the invention include, but are not d to, acetate, histidine, glycine, ne, phosphate, Tris, and citrate. In one ment, the buffer used in the formulation is histidine.

In one embodiment, the formulation comprises 1-20 mg/ml of a ine buffer (e.g., about 1 to about 20, about 1 to about 10; about 1 to about 5; or about 1 to about 3 mg/ml) with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between.

In one embodiment, the formulation comprises about 5-25 mM histidine (e.g., about 2 to about 25 mM; about 5 to about 25 mM; about 10 to about 25 mM; or about 20 to about 25 mM), and ranges in between.

In one embodiment, the formulation comprises 1-20 mg/ml of succinate buffer (e.g., about 1 to about 20, about 1 to about 10; about 5 to about 20; or about 5 to about 10 mg/ml) with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between. In one embodiment, the formulation comprises about 1-10 mg/ml of a succinate buffer with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between.

In one embodiment, the formulation comprises 1-20 mg/ml of a citrate buffer (e.g. about 1 to about 20, about 1 to about 10; about 5 to about 20; or about 5 to about 10 mg/ml) with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between. In one embodiment, the buffer used in the formulation comprises about 1-10 mg/ml of a citrate buffer with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between.

In one embodiment, the formulation comprises 1-20 mg/ml of a phosphate buffer (e.g. about 1 to about 20, about 1 to about 10; about 5 to about 20; or about 5 to about 10 mg/ml) with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in n. In one embodiment, the buffer used in the formulation comprises about 1-10 mg/ml of a phosphate buffer with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between.

In one embodiment, the formulation comprises 1-20 mg/ml of a citrate / phosphate buffer (e.g. about 1 to about 20, about 1 to about 10; about 5 to about 20; or about 5 to about mg/ml) with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about .5 to about 6.5. In one embodiment, the buffer used in the formulation comprises about 1-10 mg/ml of a citrate / phosphate buffer with a pH of about 5.0 to about 7.0; a pH of about 5 to about 6.5; or a pH of about 5.5 to about 6.5, and ranges in between.

In addition to the buffer, a sugar is included the formulation. Examples of sugars that may be used in the formulation include, but are not limited to mannitol, sorbitol, sucrose and trehalose. In one embodiment, the sugar used in the formulation is sucrose.

In one embodiment, the formulation comprises a sugar at a concentration of about 50 to about 90 mg/ml, about 50 to about 85 mg/ml, about 50 to about 80 mg/ml, about 50 to about 75 mg/ml, about 50 to about 70 mg/ml, about 50 to about 65 mg/ml, about 50 to about 60 mg/ml, about 60 to about 90 mg/ml, about 60 to about 85 mg/ml, about 60 to about 75 mg/ml, about 60 to about 70 mg/ml, or about 60 to about 75 mg/ml, and ranges in n, e.g., about 55 to about 85 mg/ml of sugar, and ranges in n.

In one embodiment, the formulation comprises sucrose at a concentration of about 50 to about 90 mg/ml, about 50 to about 85 mg/ml, about 50 to about 80 mg/ml, about 50 to about 75 mg/ml, about 50 to about 70 mg/ml, about 50 to about 65 mg/ml, about 50 to about 60 mg/ml, about 60 to about 90 mg/ml, about 60 to about 85 mg/ml, about 60 to about 75 mg/ml, about 60 to about 70 mg/ml, or about 60 to about 75 mg/ml, and ranges in between, e.g., about 55 to about 85 mg/ml of sucrose, and ranges in between.

A tant is also be added to the formulation , e.g., for added stability. Exemplary surfactants e, but are not limited to, nonionic detergents such as polysorbates (e.g., polysorbates 20, 80) or poloxamers (e.g., poloxamer 188).

In one embodiment, the formulation comprises a rbate, e.g., polysorbate 80, at a concentration of about 0.05-0.20 mg/ml (e.g. about 0.05-0.19, 0.05-0.18, 0.05-0.17, 0.05- 0.16, 0.05-0.15, 0.05-0.14, 0.05-0.13, .12, 0.05- 0.11, or 0.05-0.10 mg/ml, and ranges in between). In one embodiment, the aqueous formulation comprises 0.05-0.15 mg/ml of the polysorbate, e.g., polysorbate 80.

In one embodiment, the formulation comprises an GFR antibody drug conjugate at a concentration of about 1-150 mg/ml (e.g. about 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 120, 125, 130, 135, 140, 145, or 150 mg/ml, and values in between, of the anti-EGFR antibody drug conjugate).

In one embodiment, the formulation comprises an anti-EGFR antibody drug conjugate in an amount of about 1-150 mg, about 10-150 mg, about 20-150 mg, about 30-150 mg, about 40-150 mg, about 50-150 mg, about 60-150 mg, about 70-150 mg, about 80-150 mg, about 90-150 mg, about 100-150 mg, about 10-140 mg, about 20-140 mg, about 30-140 mg, about 40-140 mg, about 50-140 mg, about 60-140 mg. about 70-140 mg, about 80-140 mg, about 90-140 mg, about 0 mg, about 10-130 mg, about 20-130 mg, about 30-130 mg, about 40-130 mg, about 50-130 mg, about 60-130 mg about 70-130 mg, about 80-130 mg, about 90-130 mg, about 100-130 mg, about 10-120 mg, about 20-120 mg, about 30-120 mg, about 40-120 mg, about 50-120 mg, about 60-120 mg, about 70-120 mg, about 80-120 mg, about 90-120 mg, about 100-120 mg, about 10-110 mg, about 20-110 mg, about 30-110 mg, about 40-110 mg, about 50-110 mg, about 60-110 mg, about 70-110 mg, about 80-110 mg, about 90-110 mg, and about 100-110 mg, and ranges in between.

In one embodiment, the formulation comprises an anti-EGFR dy drug conjugate at a concentration of 1 mg/ml, 2 mg/ml, 3 mg/ml, 4 mg/ml, 5 mg/ml, 6 mg/ml, 7 mg/ml, 8 mg/ml, 9 mg/ml, 10 mg/ml, 11 mg/ml, 12 mg/ml, 13 mg/ml, 14 mg/ml, 15 mg/ml, 16 mg/ml, 17 mg/ml, 18 mg/ml, 19 mg/ml, 20 mg/ml, 21 mg/ml, 22 mg/ml, 23 mg/ml, 24 mg/ml, 25 mg/ml, 26 mg/ml, 27 mg/ml, 28 mg/ml, 29 mg/ml, 30 mg/ml, 31 mg/ml, 32 mg/ml, 33 mg/ml, 34 mg/ml, 35 mg/ml, 36 mg/ml, 37 mg/ml, 38 mg/ml, 39 mg/ml, 40 mg/ml, 41 mg/ml, 42 mg/ml, 43 mg/ml, 44 mg/ml, 45 mg/ml, 46 mg/ml, 47 mg/ml, 48 mg/ml, 49 mg/ml, 50 mg/ml, 51 mg/ml, 52 mg/ml, 53 mg/ml, 54 mg/ml, 55 mg/ml, 56 mg/ml, 57 mg/ml, 58 mg/ml, 59 mg/ml, 60 mg/ml, 61 mg/ml, 62 mg/ml, 63 mg/ml, 64 mg/ml, 65 mg/ml, 66 mg/ml, 67 mg/ml, 68 mg/ml, 69 mg/ml, 70 mg/ml, 71 mg/ml, 72 mg/ml, 73 mg/ml, 74 mg/ml, 75 mg/ml, 76 mg/ml, 77 mg/ml, 78 mg/ml, 79 mg/ml, 80 mg/ml, 81 mg/ml, 82 mg/ml, 83 mg/ml, 84 mg/ml, 85 mg/ml, 86 mg/ml, 87 mg/ml, 88 mg/ml, 89 mg/ml, 90 mg/ml, 91 mg/ml, 92 mg/ml, 93 mg/ml, 94 mg/ml, 95 mg/ml, 96 mg/ml, 97 mg/ml, 98 mg/ml, 99 mg/ml, 100 mg/ml, 101 mg/ml, 102 mg/ml, 103 mg/ml, 104 mg/ml, 105 mg/ml, 106 mg/ml, 107 mg/ml, 108 mg/ml, 109 mg/ml, 110 mg/ml, 111 mg/ml, 112 mg/ml, 113 mg/ml, 114 mg/ml, 115 mg/ml, 116 mg/ml, 117 mg/ml, 118 mg/ml, 119 mg/ml, 120 mg/ml, 121 mg/ml, 122 mg/ml, 123 mg/ml, 124 mg/ml, 125 mg/ml, 126 mg/ml, 127 mg/ml, 128 mg/ml, 129 mg/ml, 130 mg/ml, 131 mg/ml, 132 mg/ml, 133 mg/ml, 134 mg/ml, 135 mg/ml, 136 mg/ml, 137 mg/ml, 138 mg/ml, 139 mg/ml, 140 mg/ml, 141 mg/ml, 142 mg/ml, 143 mg/ml, 144 mg/ml, 145 mg/ml, 146 mg/ml, 147 mg/ml, 148 mg/ml, 149 mg/ml or 150 mg/ml of the antibody. Ranges including any of the aforementioned numbers are also included in the invention, e.g., 10-150 mg/ml, 10-100 mg/ml, 20-90 mg/ml, 10-70 mg/ml, 10- 40 mg.ml, and 1-70 mg/ml.

In one aspect, the invention features an aqueous formulation which is reconstituted from a lyophilized formulation comprising an anti-EGFR antibody drug conjugate, n the reconstituted aqueous formulation comprises about 1 - 100 mg/ml of the anti-EGFR ADC, about 1 -10 mg/mL of a buffer (e.g., ine), about 50 -90 mg/ml of a sugar (e.g., e), and about 0.01 - 0.2 mg/ml of a polysorbate (e.g., rbate 80), and has a pH of about 5 – 7, and wherein said anti-EGFR antibody drug conjugate comprises an anti-EGFR antibody, or antigen-binding n thereof, (e.g., antibody 1) conjugated to an atin (e.g., MMAF).

A lyophilized ation is initially made as a pre-lyophilized formulation, which is the ation prior to the lyophilization process. The amount of anti-EGFR antibody drug conjugate present in the pre-lyophilized formulation is determined taking into account the desired dose volumes, mode(s) of administration etc.

In one aspect, the invention features a lyophilized formulation comprising an anti- EGFR dy drug conjugate, a sugar, (e.g., sucrose), a surfactant, (e.g., polysorbate 80), and histidine, wherein the formulation has a pH of about 5.0 to 7.0, and wherein the anti- EGFR antibody drug conjugate comprises an anti-EGFR antibody, (e.g., antibody 1), conjugated to an auristatin, (e.g., MMAF).

In one embodiment of the invention, the lyophilized formulation comprises an anti- EGFR ADC, e.g., ADC1-MMAF, sucrose, a polysorbate, e.g., polysorbate 80, and histidine, and does not include, or is substantially free of, mannitol and/or serine. In one embodiment of the invention, the lyophilized formulation comprises an anti-EGFR ADC, e.g., ADC1- MMAF, sucrose, a polysorbate, e.g., polysorbate 80, and histidine, and does not include or is substantially free of a divalent cation. In another embodiment of the invention, the lyophilized formulation does not include lactobionic acid. In another embodiment of the invention, the lyophilized formulation does not include a sugar acid.

In certain exemplary aspects, the invention es a lyophilized formulation having a pH g from about 5.0 to 7.0 and comprising 1-20 mg of a buffer (e.g., histidine), about 320-410 mg of a sugar (e.g., sucrose), about 0.1 to 0.9 mg of a surfactant (e.g., polysorbate 80), and about 50-150 mg of an anti-EGFR antibody drug conjugate, wherein the anti-EGFR antibody drug conjugate ses an anti-EGFR antibody, (e.g., antibody 1), ated to an auristatin, (e.g., MMAF).

In one embodiment, the lyophilized formulation ses about 320-410 mg, about 330-400 mg, about 340 to 390 mg, about 350 to 380 mg, or about 360 to 370 mg of a sugar (e.g., sucrose), and ranges (e.g., 355 mg to 375 mg) in between.

In one embodiment, the lized formulation comprises about 0.1-0.9 mg of a surfactant (e.g. about 0.1-0.8, 0.1-0.7, .6, .55, 0.2-0.6, 0.3-0.6, 0.4-0.6, and ranges in between).

In one embodiment, the lyophilized formulation comprises an anti-EGFR dy drug conjugate in an amount of about 1-150 mg, about 10-150 mg, about 20-150 mg, about 30-150 mg, about 40-150 mg, about 50-150 mg, about 60-150 mg, about 70-150 mg, about 80-150 mg, about 90-150 mg, about 100-150 mg, about 10-140 mg, about 20-140 mg, about -140 mg, about 40-140 mg, about 50-140 mg, about 60-140 mg, about 70-140 mg, about 80-140 mg, about 90-140 mg, about 100-140 mg, about 10-130 mg, about 20-130 mg, about -130 mg, about 40-130 mg, about 50-130 mg, about 60-130 mg about 70-130 mg, about 80-130 mg, about 90-130 mg, about 100-130 mg, about 10-120 mg, about 20-120 mg, about -120 mg, about 40-120 mg, about 50-120 mg, about 60-120 mg, about 70-120 mg, about 80-120 mg, about 90-120 mg, about 100-120 mg, about 10-110 mg, about 20-110 mg, about -110 mg, about 40-110 mg, about 50-110 mg, about 60-110 mg, about 70-110 mg, about 80-110 mg, about 90-110 mg, and about 100-110 mg, and ranges in between.

In one embodiment, the lyophilized formulation comprises 1-20 mg/ml of histidine, or alternatively, 2-18 mg, 3-17 mg, 4-16 mg, 5-15 mg, 6-14 mg, or 7-13 mg, and ranges in between.

Lyophilization may be performed according to methods known in the art. For example, many different freeze-dryers are available for this purpose such as HULL50 (Hull, USA) or GT20 (Leybold-Heraeus, Germany) freeze-dryers. Freeze-drying is accomplished by freezing the ation and subsequently subliming ice from the frozen content at a temperature suitable for primary drying. Under this condition, the product temperature is below the eutectic point or the se temperature of the formulation. Typically, the shelf temperature for the primary drying will range from about -30 to 25°C. (provided the product remains frozen during primary drying) at a suitable pressure, ranging typically from about 50 to 250 mTorr. The ation, size and type of the container g the sample (e.g., glass vial) and the volume of liquid will mainly dictate the time required for drying, which can range from a few hours to several days (e.g. 40-60 hrs). Optionally, a secondary drying stage may also be performed depending upon the desired al moisture level in the product.

The temperature at which the secondary drying is carried out ranges from about 0-40°C, ing ily on the type and size of container and the type of protein employed. For example, the shelf temperature throughout the entire water removal phase of lyophilization may be from about 15-30°C (e.g., about 20°C). The time and pressure required for secondary drying will be that which produces a suitable lyophilized cake, dependent, e.g., on the temperature and other ters. The secondary drying time is dictated by the desired residual moisture level in the product and typically takes at least about 5 hours (e.g. 10-15 hours). The re may be the same as that employed during the primary drying step.

Freeze-drying conditions can be varied depending on the formulation and vial size.

Prior to administration to the patient, the lyophilized formulation is reconstituted with a pharmaceutically acceptable diluent such that the concentration of the anti-EGFR antibody drug ate in the reconstituted formulation is, for example, with that necessary for treatment, e.g., at least about 1-150 mg/ml. Reconstitution lly takes place at a temperature of about 25º C to ensure complete hydration, although other atures may be employed as desired. The time required for reconstitution will depend, e.g., on the type of diluent, amount of excipient(s) and protein. Exemplary diluents include sterile water, bacteriostatic water for injection (BWFI), a pH buffered solution (e.g. phosphate-buffered saline), sterile saline solution (e.g., 0.9% saline solution), Ringer's on or dextrose on. In one embodiment, the lyophilisates are to be dissolved in sterile water for injection and diluted in sterile Normal Saline solution. The diluent optionally contains a preservative. ary vatives have been described above, with aromatic alcohols such as benzyl or phenol alcohol being the preferred preservatives. The amount of preservative employed is determined by assessing different preservative concentrations for compatibility with the protein and preservative efficacy testing. For example, if the preservative is an aromatic alcohol (such as benzyl alcohol), it can be present in an amount from about 0.1-2.0%, from about 0.5-1.5%, or about 2%.

III. GFR Antibody Drug Conjugates for Use in the Formulations of the Invention The formulations and methods described herein encompass the use of antibody drug conjugates (ADCs) comprising anti-EGFR antibodies, or antigen-binding portions f, that specifically bind to EGFR. The anti-EGFR antibody drug conjugates used in the formulations of the invention are conjugated to a therapeutic agent, whereby the therapeutic agent exerts a cytotoxic, atic or suppressive effect on EGFR-expressing cells.

In particular, the t invention pertains to formulations comprising an anti-EGFR antibody drug conjugate comprising an antibody, or an antigen-binding portion thereof, that recognizes an EGFR epitope which is found in tumorigenic, hyperproliferative or abnormal cells, wherein the epitope is not detectable in normal or wild-type cells. Preferably, the antibody or antigen-binding portion thereof, does not bind to or ize normal or wildtype cells containing normal or wild-type EGFR epitope in the absence of overexpression and in the presence of normal EGFR post-translational modification.

Anti-EGFR antibodies suitable for use in accordance with the present formulations and methods are typically monoclonal and can include, for example, chimeric (e.g., having a human constant region and mouse variable region), humanized, or human antibodies; single chain antibodies; or the like. The immunoglobulin les can be of any type (e.g., IgG, IgE, IgM, IgD, IgA and IgY), class (e.g., IgG1, IgG2, IgG3, IgG4, IgA1 and IgA2) or subclass of immunoglobulin molecule. For example, the anti-EGFR antibody used in the anti-EGFR antibody drug conjugate of the invention may be GFR antibody 1 or 2, or an antigen-binding portion thereof. The sequences and characteristics of antibodies 1 and 2 are described below (see also sequence of Figure 55), incorporated by reference in their ty ). Antibodies 1 and 2 each target the over-expressed form of the epidermal growth factor receptor (EGFR) present in 50% of all cancers of epithelial .

In a particular embodiment of the present invention, the anti-EGFR antibody used in the anti-EGFR antibody drug conjugate recognizes ied wild-type EGFR and the de2-7 EGFR. The GFR antibody (or GFR ADC) demonstrates useful specificity, in that it recognizes de2-7 EGFR and amplified EGFR, but does not recognize normal, wildtype EGFR or the unique onal peptide which is characteristic of de2-7 EGFR. es of antibodies having these binding characteristics are antibody 1, antibody 2 and antibody 3. Sequences for antibody 1 and antibody 2 are provided below.

Antibody 2 is a monoclonal murine anti-EGFR antibody. The antibody 2 VH chain comprises nucleic acid sequence (SEQ ID NO: 1) and amino acid sequence, with signal peptide (SEQ ID NO: 2) as shown below (signal peptide underlined in SEQ ID NO: 2).

SEQ ID NO: 1 ATGAGAGTGCTGATTCTTTTGTGGCTGTTCACAGCCTTTCCTGGTGTCCTGTCTGA TGTGCAGCTTCAGGAGTCGGGACCTAGCCTGGTGAAACCTTCTCAGTCTCTGTCC CTCACCTGCACTGTCACTGGCTACTCAATCACCAGTGATTTTGCCTGGAACTGGA TCCGGCAGTTTCCAGGAAACAAGCTGGAGTGGATGGGCTACATAAGTTATAGTG GTAACACTAGGTACAACCCATCTCTCAAAAGTCGAATCTCTATCACTCGAGACAC ATCCAAGAACCAATTCTTCCTGCAGTTGAATTCTGTGACTATTGAGGACACAGCC ACATATTACTGTGTAACGGCGGGACGCGGGTTTCCTTATTGGGGCCAAGGGACTC TGGTCACTGTCTCTGCA SEQ ID NO: 2 MRVLILLWLFTAFPGVLSDVQLQESGPSLVKPSQSLSLTCTVTGYSITSDFAWNWIRQ FPGNKLEWMGYISYSGNTRYNPSLKSRISITRDTSKNQFFLQLNSVTIEDTATYYCVT AGRGFPYWGQGTLVTVSA The antibody 2 VL chain comprises nucleic acid sequence (SEQ ID NO: 3) and amino acid sequence (SEQ ID NO :4) as shown below (signal peptide underlined in SEQ ID NO: 4).

SEQ ID NO: 3 ATGGTGTCCACAGCTCAGTTCCTTGCATTCTTGTTGCTTTGGTTTCCAGGTGCAAG ATGTGACATCCTGATGACCCAATCTCCATCCTCCATGTCTGTATCTCTGGGAGAC ACAGTCAGCATCACTTGCCATTCAAGTCAGGACATTAACAGTAATATAGGGTGGT TGCAGCAGAGACCAGGGAAATCATTTAAGGGCCTGATCTATCATGGAACCAACT TGGACGATGAAGTTCCATCAAGGTTCAGTGGCAGTGGATCTGGAGCCGATTATTC CATCAGCAGCCTGGAATCTGAAGATTTTGCAGACTATTACTGTGTACAG TATGCTCAGTTTCCGTGGACGTTCGGTGGAGGCACCAAGCTGGAAATCAAACGT SEQ ID NO: 4 MVSTAQFLAFLLLWFPGARCDILMTQSPSSMSVSLGDTVSITCHSSQDINSNIGWLQQ RPGKSFKGLIYHGTNLDDEVPSRFSGSGSGADYSLTISSLESEDFADYYCVQYAQFPW TFGGGTKLEIKR Complementarity determining s CDR1, CDR2, and CDR3 (SEQ ID NOs: 5, 6, and 7, respectively) of the VH chain sequence SEQ ID NO: 2, without signal peptide (SEQ ID NO: 11) are indicated by underlining below. Key residues of the VH chain sequence (SEQ ID NO: 11) are 24, 37, 48, 67 and 78.

SEQ ID NO: 11 DVQLQESGPSLVKPSQSLSLTCTVTGYSITSDFAWNWIRQFPGNKLEWMGYISYSGNTR CDR1 CDR2 YNPSLKSRISITRDTSKNQFFLQLNSVTIEDTATYYCVTAGRGFPYWGQGTLVTVSA Complementarity determining regions CDR1, CDR2, and CDR3 (SEQ ID NOS: 8, 9, and 10, tively) of the VL chain sequence SEQ ID NO :4, without signal peptide (SEQ ID NO: 12) are indicated by underlining below. Key residues of the VH chain sequence (SEQ ID NO: 12) are 36, 46, 57 and 71.

SEQ ID NO: 12 DILMTQSPSSMSVSLGDTVSITCHSSQDINSNIGWLQQRPGKSFKGLIYHGTNLDDEVPSR CDR1 CDR2 FSGSGSGADYSLTISSLESEDFADYYCVQYAQFPWTFGGGTKLEIKR Antibody 3 is a ic antibody comprising the variable domains of the light and heavy chains of antibody 2, and human constant regions.

In one embodiment of the invention, the anti-EGFR antibody used in the formulations and methods of the invention is dy 1. As described above, antibody 1 is a humanized anti-EGFR antibody which includes the CDRs of antibody 2. The heavy chain variable (VH) and constant (CH) regions of antibody 1 are shown below as SEQ ID NOS: 13 and 14, respectively. The VH region CDR1, CDR2, and CDR3 (SEQ ID NOS: 15, 16, and 17, respectively) are indicated by underlining.

SEQ ID NO: 13 QVQLQESGPGLVKPSQTLSLTCTVSGYSISSDFAWNWIRQPPGKGLEWMGYISYSGNTR CDR1 CDR2 SRITISRDTSKNQFFLKLNSVTAADTATYYCVTAGRGFPYWGQGTLVTVSS SEQ ID NO: 14 ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVL QSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAP ELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKT KPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREP QVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGS FFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK The light chain variable (VL) and constant (CL) regions of antibody 1 are shown below as SEQ ID NOS: 18 and 19, respectively. The VL region CDR1, CDR2, and CDR3 (SEQ ID NOS: 20, 21, and 22, respectively) are indicated by underlining.

SEQ ID NO: 18 DIQMTQSPSSMSVSVGDRVTITCHSSQDINSNIGWLQQKPGKSFKGLIYHGTNLDDGVPS CDR1 CDR2 RFSGSGSGTDYTLTISSLQPEDFATYYCVQYAQFPWTFGGGTKLEIKR CDR3 SEQ ID NO: 19 TVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTE QDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC In one embodiment, the invention features a lyophilized formulation comprising an anti-EGFR antibody drug conjugate, sucrose, polysorbate 80, and histidine, wherein the formulation has a pH of about 5 -7, wherein the anti-EGFR antibody drug conjugate ses an anti-EGFR antibody, or antigen g portion f, conjugated to monomethyl auristatin F , and wherein said antibody comprises a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid sequences set forth in SEQ ID NOS: 15, 16, and 17, and comprises a light chain variable region comprising CDRs comprising the amino acid ces set forth in SEQ ID NOS: 20, 21, and 22.

In one ment, the invention provides a lyophilized formulation having a pH of about 5-7 and comprising an anti-EGFR ADC comprising an antibody, or antigen-binding n thereof, comprising a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO: 13 and a heavy chain constant region having the amino acid sequence as set forth in SEQ ID NO: 14, and a light chain variable region having the amino acid sequence set forth in SEQ ID NO: 18 and a light chain constant region having the amino acid sequence as set forth in SEQ ID NO: 19, histidine, a sugar, e.g., sucrose, and a polysorbate, e.g., polysorbate 80.

In one embodiment, the invention provides a ation comprising an ADC sing an anti-EGFR antibody (conjugated to an auristatin, e.g., MMAF) having a light chain variable region comprising CDRs as described in the amino acid sequence of SEQ ID NO: 18, a heavy chain variable region comprising CDRs as described in the amino acid sequence of SEQ ID NO: 13.

GFR antibodies that may be used make anti-EGFR antibody drug conjugates can be generated by any suitable method known in the art. For example, monoclonal antibodies can be prepared using a wide variety of techniques including, e.g., the use of hybridoma, recombinant, and phage display technologies, or a ation thereof.

Hybridoma techniques are generally discussed in, for example, Harlow et al., Antibodies: A Laboratory Manual, (Cold Spring Harbor Laboratory Press, 2nd ed., 1988); and Hammerling, et al., In onal Antibodies and T-Cell Hybridomas, pp. 563-681 (Elsevier, N.Y., 1981).

Examples of phage display s that can be used to make the anti-CD70 antibodies include, e.g., those disclosed in Brinkman et al., 1995, J Immunol Methods 182:41-50; Ames et al., 1995, J Immunol Methods 184:177-186; Kettleborough et al., 1994, Eur J Immunol 24:952-958; Persic et al., 1997, Gene 18; Burton et al., 1994, Advances in Immunology -280; PCT Application No. PCT/GB91/01 134; PCT Publications WO 90/02809; WO 91/10737; WO 92/01047; WO 92/18619; WO 93/11236; WO 95/15982; WO 95/20401; and U.S. Pat. Nos. 426; 5,223,409; 5,403,484; 5,580,717; 908; 5,750,753; 5,821,047; 698; 5,427,908; 5,516,637; 5,780,225; 5,658,727; 5,733,743 and ,969,108 (the disclosures of which are incorporated by reference herein).

Techniques for generating antibody fragments that recognize specific epitopes are also generally known in the art. For example, Fab and F(ab')2 fragments can be ed by proteolytic cleavage of immunoglobulin molecules, using enzymes such as papain (to produce Fab fragments) or pepsin (to e F(ab')2 fragments). F(ab')2 fragments contain the variable region, the light chain constant region and the CH1 domain of the heavy chain.

Techniques to recombinantly produce Fab, Fab' and F(ab')2 fragments can also be employed using, e.g., methods disclosed in PCT ation WO 92/22324; Mullinax et al., 1992, hniques 12(6):864-869; and Sawai et al., 1995, AJRI 34; and Better et al., 1988, Science 41-1043 (the disclosures of which are incorporated by reference herein).

Examples of techniques that can be used to produce single-chain Fvs and dies include those described in U.S. Pat. Nos. 4,946,778 and 5,258,498; Huston et al., 1991, Methods in Enzymology 203:46-88; Shu et al., 1993, Proc Natl Acad Sci USA 90:7995-7999; and Skerra et al., 1988, Science 240:1038-1040.

Antibodies may be produced by any of a number of techniques known in the art. For example, expression from host cells, wherein expression vector(s) encoding the heavy and light chains is (are) transfected into a host cell by standard techniques. The various forms of the term "transfection" are intended to encompass a wide variety of techniques commonly used for the introduction of exogenous DNA into a prokaryotic or eukaryotic host cell, e.g., electroporation, calcium-phosphate precipitation, DEAE-dextran transfection and the like.

Mammalian host cells for expressing the recombinant antibodies of the invention e Chinese r Ovary (CHO cells) (including dhfr-CHO cells, described in Urlaub and Chasin (1980) Proc. Natl. Acad. Sci. USA 77:4216-4220, used with a DHFR selectable marker, e.g., as described in Kaufman and Sharp (1982) J. Mol. Biol. 1-621) and DG44 or DUXB11 cells (Urlaub et al. (1986) Som. Cell Molec. Genet. 12:555; Haynes et al. (1983) Nuc. Acid. Res. 11:687-706; Lau et al. (1984) Mol. Cell. Biol. 4:1469-1475), NS0 a cells, monkey kidney line (e.g., CVI and COS, such as a COS 7 cell), SP2 cells, human embryonic kidney (HEK) cells, such as a HEK-293 cell, Chinese hamster fibroblast (e.g., R1610), human cervical carcinoma (e.g., HELA), murine fibroblast (e.g., BALBc/3T3), murine myeloma (P3x63-Ag3.653; NS0; SP2/O), hamster kidney line (e.g., HAK), murine L cell (e.g., L-929), human lymphocyte (e.g., RAJI), human kidney (e.g., 293 and 293T). Host cell lines are typically commercially ble (e.g., from BD Biosciences, Lexington, Ky.; Promega, n, Wis.; Life Technologies, rsburg, Md.) or from the American Type Culture Collection (ATCC, Manassas, Va.).

When recombinant expression vectors encoding the antibody are introduced into mammalian host cells, the antibodies are produced by culturing the host cells for a period of time sufficient to allow for expression of the antibodies in the host cells or secretion of the antibodies into the culture medium in which the host cells are grown. Antibodies can be red from the culture medium using standard protein cation methods.

In an exemplary system for recombinant expression of antibodies, a recombinant expression vector encoding both the antibody heavy chain and the antibody light chain is introduced into dhfr-CHO cells by calcium phosphate-mediated transfection. Within the recombinant expression , the antibody heavy and light chain cDNAs are each operatively linked to CMV enhancer/AdMLP promoter regulatory elements to drive high levels of transcription of the cDNAs. The recombinant expression vector also carries cDNA ng DHFR, which allows for selection of CHO cells that have been transfected with the vector using rexate selection/amplification. The selected transformant host cells are ed to allow for expression of the antibody heavy and light chains and intact antibody is recovered from the culture medium. Standard molecular biology techniques are used to prepare the recombinant expression vector, transfect the host cells, select for transformants, culture the host cells and recover the antibody from the culture medium. Still r, the invention provides a method of sizing an antibody by ing a host cell of the invention in a suitable culture medium until the antibody is synthesized. The method can further comprise isolating the antibody from the culture medium.

The anti-EGFR antibody drug ate used in the invention comprises an anti- EGFR antibody, or antigen binding portion thereof, conjugated to a cytotoxic or immunosuppressive agent, such that the resulting ADC exerts a cytotoxic or atic effect on an EGFR-expressing cancer cell. Thus, the anti-EGFR antibody drug conjugate exerts a cytotoxic or cytostatic effect on EGFR-expressing cancer cells. In one embodiment, the anti- EGFR ADC is internalized and accumulates within an EGFR-expressing cell, where the ADC exerts a therapeutic effect (e.g., a cytotoxic, cytostatic, or immunosuppressive effect). es of suitable moieties for conjugation to antibodies include chemotherapeutic agents, g converting enzymes, radioactive isotopes or compounds, or toxins. In exemplary embodiments, the anti-EGFR antibody, or an antigen-binding portion f is ated to an atin, e.g., MMAF or MMAE. Any agent that exerts a therapeutic effect on cancer cells or activated immune cells can be used as the therapeutic agent for conjugation to an anti-EGFR antibody or derivative f. (See, e.g., "Drug Conjugates and Their Use for Treating Cancer, An Autoimmune. Disease or an Infectious Disease" (supra) and U.S. Provisional Application No. 60/400,403 (supra)).

Typically, the therapeutic agent is a cytotoxic agent. In some embodiments, an anti-EGFR drug conjugate comprises more than one therapeutic agents per conjugate, for example from about 1 to about 20 therapeutic agents per conjugate.

In a preferred embodiment, the anti-EGFR dy, or an antigen-binding portion thereof, is conjugated to an auristatin (one or more). Auristatins have been shown to interfere with microtubule dynamics, GTP hydrolysis, and/or nuclear and cellular division and have anticancer and/or antifungal activity.

An anti-EGFR antibody of the ion may be conjugated to at least one auristatin.

Auristatins represent a group of dolastatin analogs that have generally been shown to possess anticancer activity by interfering with microtubule dynamics and GTP hydrolysis, thereby inhibiting cellular division. For example, Auristatin E (described in U.S. Patent No. ,635,483, incorporated by reference ) is a synthetic analogue of the marine natural product dolastatin 10, a compound that inhibits n polymerization by binding to the same site on n as the anticancer drug vincristine (G. R. Pettit, Prog. Chem. Org. Nat. Prod, 70: 1-79 (1997)). Dolastatin 10, auristatin PE, and auristatin E are linear peptides having four amino acids, three of which are unique to the atin class of compounds. Exemplary embodiments of the auristatin ss of mitotic inhibitors include, but are not limited to, monomethyl auristatin D (MMAD or atin D derivative), monomethyl auristatin E (MMAE or auristatin E derivative), monomethyl auristatin F (MMAF or auristatin F derivative), auristatin F phenylenediamine (AFP), auristatin EB (AEB), auristatin EFP , and 5-benzoylvaleric acid-AE ester (AEVB). The synthesis and structure of auristatin derivatives are described in U.S. Patent Application Publication Nos. 2003- 0083263, 2005-0238649 and 009751; International Patent Publication No. WO 04/010957, International Patent Publication No. WO 02/088172, and U.S. Pat. Nos. 6,323,315; 104; 6,034,065; 5,780,588; 5,665,860; 5,663,149; 5,635,483; 5,599,902; ,554,725; 5,530,097; 5,521,284; 5,504,191; 5,410,024; 5,138,036; 5,076,973; 4,986,988; 744; 4,879,278; 4,816,444; and 4,486,414, each of which is incorporated by reference herein.

In one ment, an anti-EGFR antibody, such as antibody 1, is conjugated to at least one MMAF (monomethyl auristatin F) by a linker such as, but not limited to, maleimidocaproyl (mc-MMAF). The structure of MMAF is provided in Figure 2. An anti- EGFR-antibody ADC may have a drug-to-antibody ratio (DAR) of 2, 4, 6, or 8. Notably, the DAR of an ADC can range from 0 to 8, although higher loads, e.g., 10, are also possible.

Monomethyl atin F (MMAF) inhibits cell division by blocking the polymerization of tubulin. It has a charged C-terminal phenylalanine residue that ates its cytotoxic activity compared to its uncharged counterpart MMAE. Because of its toxicity, it cannot be used as a drug itself, but can be linked to a monoclonal antibody (mAb) that directs it to the cancer cells. In one embodiment, the linker to the anti-EGFR antibody is stable in extracellular fluid, but is cleaved by cathepsin once the conjugate has entered a tumor cell, thus activating the anti-mitotic mechanism.

In one ment, the anti-EGFR antibody of the invention is conjugated to at least one MMAE (mono-methyl auristatin E). The structure of MMAE is provided in Figure 1, as is an exemplary ADC sing MMAE. Monomethyl auristatin E (MMAE, vedotin) inhibits cell division by blocking the polymerisation of tubulin. Because of its super toxicity, it also cannot be used as a drug itself. In recent cancer therapy developments, it is linked to a monoclonal antibody (mAb) that recognizes a specific marker expression in cancer cells and directs MMAE to the cancer cells. In one embodiment, the linker linking MMAE to the anti- EGFR antibody is stable in extracellular fluid (i.e., the medium or environment that is external to cells), but is cleaved by cathepsin once the ADC has bound to the specific cancer cell antigen and entered the cancer cell, thus releasing the toxic MMAE and activating the potent anti-mitotic mechanism.

In one embodiment, the anti-EGFR antibody, or antigen-binding portion f, is conjugated to an auristatin which is MMAF. In one embodiment, the anti-EGFR ADC is the ADC 1-MMAF. ADC 1-MMAF comprises antibody 1 (described above and in SEQ ID NOs: 13 to 22) covalently linked to one or more molecules of monomethyl auristatin F (MMAF) (see Figure 2 for structure). To generate ADC , the interchain ide bonds of antibody 1 are d to sulfhydryl groups. MMAF is then coupled to the antibody via these sulfhydryl groups. ADC 1-MMAF is generated using a noncleavable linker, i.e., a noncleavable maleimidocaproyl (mc) linkage, as shown in Figure 2.

In one particular ment, the formulations of the invention comprise anti-EGFR ADCs that are labeled with a detectable or functional label. able labels include, but are not limited to, radiolabels such as the isotopes 2H, 3H, 11C, 13C, 14C, 32P, 33S, 34S, 35S, 36S, 36C1, 51Cr, 57Co, 58Co, 59Fe, 90Y, 121I, 124I, 125I, 131I, 211At, 198Au, 67Cu, 225Ac, 213Bi, 99Tc and 186Re, which may be ed to antibodies of the invention using conventional try known in the art of antibody imaging. Labels also include fluorescent labels and labels used conventionally in the art for MRI-CT imagine. They also include enzyme labels such as adish peroxidase. Labels further include chemical moieties such as biotin which may be detected via binding to a specific cognate detectable moiety, e.g. labeled avidin.

Functional labels may also include substances which are designed to be targeted to the site of a tumor to cause destruction of tumor tissue. Such functional labels include cytotoxic drugs such as 5-fluorouracil or ricin and enzymes such as bacterial carboxypeptidase or nitroreductase, which are capable of converting prodrugs into active drugs at the site of a tumor.

As will be understood by those of skill in the art, the agents set forth above, as well as other le agents, may be conjugated or attached to an anti-EGFR antibody, e.g., dy 1, in any suitable manner to e an anti-EGFR ADC useful in the present invention. For example and without limitation, in various embodiments of the present invention the anti- EGFR antibody and agent(s) may be covalently attached and/or may be conjugated using linker, spacer and/or stretcher compounds, which in various embodiments of the present invention are cleavable or are noncleavable, and result in the therapeutic agent(s) being internalized by the target cell.

In one embodiment, antibody 1 is conjugated to MMAF using a noncleavable maleimidocaproyl linkage (antibody 1-mc-MMAF).

Techniques for ating therapeutic agents to proteins, and in particular to antibodies, are well-known. (See, e.g., Arnon et al., "Monoclonal Antibodies For Immunotargeting Of Drugs In Cancer Therapy," in Monoclonal Antibodies And Cancer Therapy (Reisfeld et al. eds., Alan R. Liss, Inc., 1985); Hellstrom et al., "Antibodies For Drug Delivery," in Controlled Drug Delivery (Robinson et al. eds., Marcel , Inc., 2nd ed. 1987); Thorpe, "Antibody Carriers Of Cytotoxic Agents In Cancer Therapy: A Review," in Monoclonal Antibodies '84: Biological And Clinical Applications (Pinchera et al. eds., 1985); "Analysis, Results, and Future Prospective of the Therapeutic Use of Radiolabeled dy In Cancer Therapy," in Monoclonal Antibodies For Cancer Detection And Therapy (Baldwin et al. eds., Academic Press, 1985); and Thorpe et al., 1982, Immunol. Rev. 62:119- 58. See also, e.g., PCT publication WO 89/12624.) In one embodiment, the ADC comprises a linker region between the cytotoxic agent and the antibody. For example, such linker, spacer and/or her compounds include, but are not limited to, the following: amino benzoic acid spacers (see, for example and without limitation, U.S. Patent Nos. 7,091,186 and 816, each of which is hereby incorporated by reference in its entirety); maleimidocaproyl; p-aminobenzylcarbamoyl (PAB); lysosomal enzyme-cleavable linkers (see, for example and without limitation, U.S. Patent No. 6,214,345, hereby incorporated by reference in its entirety); maleimidocaproyl-polyethylene glycol (MC(PEG)6-OH); N-methyl-valine citrulline; N-succinimidyl 4-(N- maleimidomethyl) cyclohexanecarboxylate (SMCC) (see, for example and t limitation, ake et al. (1979) Eur. J. m., 101, 395-399, hereby incorporated by reference in its entirety); N- succinimidyl 4-(2-pyridyldithio) butanoate (SPDB) (see, for e and without tion, U.S. Patent No. 304, hereby incorporated by reference in its ty); N-Succinimidyl 4-(2-pyridylthio)pentanoate (SPP); valine-citrulline; and other linker, spacer, and/or stretcher compounds (see, for example and without limitation, U.S. Patent Nos. 7,090,843, 7,223,837, and 7,659,241, and U.S. Patent Publication Nos. 2004/0018194, 121940, 2006/0116422, 2007/0258987, 2008/0213289, 2008/0241128, 2008/0311136, 317747, and 2009/0010945, each of which is hereby incorporated by reference in its entirety). Generally speaking, techniques for attaching and/or ating the agents set forth above, as well as other agents, to specific binding members of the present invention, particularly antibodies and fragments thereof, are known in the art. See, for example and without limitation, Amon et al., "Monoclonal Antibodies For Immunotargeting Of Drugs In Cancer Therapy", in Monoclonal Antibodies And Cancer Therapy, Reisfeld et al. (eds.), pp. 243-56 (Alan R. Liss, Inc. 1985); Hellstrom et al., "Antibodies For Drug Delivery", in Controlled Drug Delivery (2nd Ed.), Robinson et al. (eds.), pp. 623-53 (Marcel Dekker, Inc. 1987); Thorpe, "Antibody Carriers Of Cytotoxic Agents In Cancer Therapy: A ", In Monoclonal Antibodies '84: Biological And al ations, Pinchera et al. (eds.), pp. 475-506 (1985); "Analysis, Results, And Future Prospective Of The eutic Use Of Radiolabeled Antibody In Cancer Therapy", in Monoclonal Antibodies For Cancer Detection And Therapy, Baldwin et al. (eds.), pp. 303-16 (Academic Press 1985), and Thorpe et al., "The Preparation And Cytotoxic ties Of Antibody-Toxin Conjugates", Immunol.

Rev., 62:119-58 (1982), each of which is hereby incorporated by reference in its entirety.

A number of different reactions are available for nt attachment of drugs to antibodies. This is often accomplished by reaction of the amino acid residues of the antibody molecule, ing the amine groups of lysine, the free carboxylic acid groups of glutamic and aspartic acid, the sulfhydryl groups of cysteine and the various moieties of the aromatic amino acids. One of the most commonly used ecific s of covalent attachment is the carbodiimide reaction to link a carboxy (or amino) group of a compound to amino (or carboxy) groups of the antibody. Additionally, bifunctional agents such as dialdehydes or imidoesters have been used to link the amino group of a compound to amino groups of the antibody molecule. Also ble for attachment of drugs to antibodies is the Schiff base reaction. This method es the ate oxidation of a drug that contains glycol or hydroxy groups, thus forming an de which is then reacted with the antibody molecule.

Attachment occurs via formation of a Schiff base with amino groups of the antibody molecule. Isothiocyanates can also be used as coupling agents for covalently attaching drugs to antibodies. Other techniques are known to the skilled artisan and within the scope of the present invention. Non-limiting examples of such techniques are described in, e.g., U.S. Pat.

Nos. 5,665,358; 5,643,573; and 623, which are incorporated by reference in their entireties herein.

In certain embodiments, an intermediate, which is the precursor of the linker, is reacted with the drug under appropriate conditions. In certain ments, reactive groups are used on the drug and/or the intermediate. The product of the reaction between the drug and the intermediate, or the tized drug, is subsequently reacted with the anti-EGFR antibody under appropriate conditions.

Other examples of conjugation methods are described in US Patent No. 7,837,980 (Seattle Genetics), Carter and Senter (2008) Cancer J, 154, as well as U.S. Published Application Nos. 2004-0157782 A1 and 2005-0238649 and International Patent Application No, PCT/US04/038392.

In certain embodiments, anti-EGFR ADCs may be purified in order to obtain ADCs having a desired drug to antibody ration (DAR). In one embodiment of the invention, the formulation contains an anti-EGFR ADC mixture comprising anti-EGFR ADCs having an average desired drug to antibody ration (DAR), e.g., an average DAR of about 3. In one embodiment of the invention, the ation comprises an ADC mixture comprising anti- EGFR ADCs having a desired DAR range, e.g., a DAR of about 2-4.

In one ment, the formulation contains an ADC mixture where 70% of the ADCs present have a drug loaded s of 4 or less, and wherein the ADC comprises an anti-EGFR antibody and an auristatin. Alternatively, 75% of ADCs t have a drug loaded species of 4 or less; 80% of ADCs present have a drug loaded species of 4 or less; 85% of ADCs present have a drug loaded s of 4 or less; 90% of ADCs present have a drug loaded species of 4 or less; or 95% of ADCs present have a drug loaded species of 4 or less.

In one embodiment of the invention, the formulation comprises an anti-EGFR ADC comprising an anti-EGFR antibody, or antigen-binding portion f, conjugated to monomethyl auristatin F (MMAF), n said ADC 1-MMAF comprises a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid sequences set forth in SEQ ID NOS: 15, 16, and 17, and ses a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22, sucrose, histidine, and polysorbate 80, wherein the formulation comprises an ADC mixture having an average DAR of about 3 or an ADC mixture having a DAR of about 2-4. In a further embodiment of the invention, the formulation is lyophilized. In yet a further embodiment, the anti-EGFR antibody is linked to MMAF via a maleimidocaproyl linker. In still a further embodiment, the GFR antibody, or antigen-binding portion thereof, comprises a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 13, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 18.

In one embodiment, the formulation comprises an anti-EGFR ADC sing an anti-EGFR antibody, or antigen-binding portion thereof, conjugated to monomethyl auristatin E (MMAE), wherein said ADC 1-MMAE ses a heavy chain variable region comprising complementarity domain regions (CDRs) comprising the amino acid ces set forth in SEQ ID NOS: 15, 16, and 17, and comprises a light chain le region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22, sucrose, histidine, and polysorbate 80, wherein the formulation comprises an ADC mixture having an average DAR of about 3 or an ADC e having a DAR of about 2-4.

In a further embodiment of the invention, the formulation is lized. In still a further ment, the anti-EGFR antibody, or antigen-binding portion thereof, comprises a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 13, and a light chain variable region comprising the amino acid ce set forth in SEQ ID NO: 18.

Purification of the ADCs may be achieved in such a way that ADCs having certain DARs are collected. For example, HIC resin may be used to separate high drug loaded ADCs from ADCs having optimal drug to antibody ratios (DARs), e.g. a DAR of 4 or less. In one embodiment, a hydrophobic resin is added to an ADC mixture such that undesired ADCs, i.e., higher drug loaded ADCs, bind the resin and can be selectively removed from the mixture. In certain ments, separation of the ADCs may be achieved by contacting an ADC mixture (e.g., a mixture comprising a drug loaded species of ADC of 4 or less and a drug loaded species of ADC of 6 or more) with a hobic resin, wherein the amount of resin is sufficient to allow binding of the drug loaded species which is being removed from the ADC mixture. The resin and ADC mixture are mixed together, such that the ADC species being removed (e.g., a drug loaded species of 6 or more) binds to the resin and can be separated from the other ADC species in the ADC mixture. The amount of resin used in the method is based on a weight ratio between the species to be removed and the resin, where the amount of resin used does not allow for significant binding of the drug loaded species that is desired. Thus, methods may be used to reduce the average DAR 5.5 to less than 4. Further, the purification methods may be used to isolate ADCs having any desired range of drug loaded species, e.g., a drug loaded species of 4 or less, a drug loaded s of 3 or less, a drug loaded species of 2 or less, a drug loaded species of 1 or less.

Certain species of molecule(s) binds to a surface based on hydrophobic interactions between the species and a hydrophobic resin. In one embodiment, method of the invention refers to a cation process that relies upon the ixing of a hydrophobic resin and a mixture of ADCs, n the amount of resin added to the mixture determines which species (e.g., ADCs with a DAR of 6 or more) will bind. Following production and purification of an antibody from an expression system (e.g., a mammalian expression system), the antibody is reduced and coupled to a drug through a conjugation reaction. The resulting ADC mixture often contains ADCs having a range of DARs, e.g., 1 to 8. In one embodiment, the ADC mixture ses a drug loaded species of 4 or less and a drug loaded species of 6 or more. According to the methods of the ion, the ADC mixture may be purified using a process, such as, but not d to, a batch process, such that ADCs having a drug loaded species of 4 or less are selected and separated from ADCs having a higher drug load (e.g., ADCs having a drug loaded species of 6 or more). Notably, the purification methods described herein may be used to isolate ADCs having any desired range of DAR, e.g., a DAR of 4 or less, a DAR of 3 or less, a DAR of 2 or less.

Thus, in one embodiment, an ADC mixture comprising a drug loaded species of 4 or less and a drug loaded species of 6 or more may be contacted with a hydrophobic resin to form a resin mixture, wherein the amount of hydrophobic resin contacted with the ADC e is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant binding of the drug load species of 4 or less; and removing the hydrophobic resin from the ADC mixture, such that the ition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody conjugated to an auristatin. In a separate ment, the method may include contacting an ADC mixture comprising a drug loaded species of 4 or less and a drug loaded species of 6 or more with a hydrophobic resin to form a resin mixture, wherein the amount of hydrophobic resin ted with the ADC mixture is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant g of the drug load species of 4 or less; and removing the hydrophobic resin from the ADC mixture, such that the composition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody conjugated to an auristatin, n the hydrophobic resin weight is 3 to 12 times the weight of the drug loaded s of 6 or more in the ADC mixture.

The ADC tion method may be performed using a batch purification method.

The batch purification process generally includes adding the ADC mixture to the hydrophobic resin in a vessel, mixing, and subsequently ting the resin from the atant. For example, in the context of batch purification, a hydrophobic resin may be prepared in or brated to the desired equilibration . A slurry of the hobic resin may thus be obtained. The ADC mixture may then be contacted with the slurry to adsorb the specific species of ADC(s) to be separated by the hydrophobic resin. The solution comprising the desired ADCs that do not bind to the hydrophobic resin material may then be separated from the slurry, e.g., by filtration or by allowing the slurry to settle and removing the supernatant. The resulting slurry can be subjected to one or more washing steps. In order to elute bound ADCs, the salt concentration can be sed. In one embodiment, the s used in the invention includes no more than 50 g of hydrophobic resin.

Thus, a batch method may be used to contact an ADC mixture comprising a drug loaded s of 4 or less and a drug loaded species of 6 or more with a hydrophobic resin to form a resin mixture, wherein the amount of hydrophobic resin contacted with the ADC mixture is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant binding of the drug load species of 4 or less; and removing the hydrophobic resin from the ADC mixture, such that the composition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody conjugated to an auristatin. In a separate embodiment, a batch method is used to contact an ADC mixture comprising a drug loaded species of 4 or less and a drug loaded species of 6 or more with a hydrophobic resin to form a resin mixture, wherein the amount of hydrophobic resin contacted with the ADC mixture is ient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant binding of the drug load species of 4 or less; and removing the hobic resin from the ADC mixture, such that the composition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody conjugated to an auristatin, wherein the hydrophobic resin weight is 3 to 12 times the weight of the drug loaded species of 6 or more in the ADC mixture.

Alternatively, purification may be performed using a circulation process, whereby the resin is packed in a container and the ADC mixture is passed over the hydrophobic resin bed until the specific s of ADC(s) to be separated have been removed. The supernatant (containing the desired ADC species) is then pumped from the container and the resin bed may be subjected to washing steps.

A circulation process may also be used to contact an ADC mixture comprising a drug loaded species of 4 or less and a drug loaded species of 6 or more with a hydrophobic resin to form a resin mixture, wherein the amount of hydrophobic resin contacted with the ADC mixture is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant binding of the drug load s of 4 or less; and removing the hydrophobic resin from the ADC mixture, such that the composition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody ated to an auristatin. In a te embodiment, a circulation process is used to t an ADC mixture sing a drug loaded species of 4 or less and a drug loaded s of 6 or more with a hydrophobic resin to form a resin mixture, wherein the amount of hobic resin contacted with the ADC mixture is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant g of the drug load species of 4 or less; and removing the hydrophobic resin from the ADC mixture, such that the composition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody conjugated to an atin, wherein the hydrophobic resin weight is 3 to 12 times the weight of the drug loaded species of 6 or more in the ADC e.

Alternatively, purification may be performed using a flow through process, whereby resin is packed in a container, e.g., a column, and the ADC mixture is passed over the packed resin such that the desired ADC species does not substantially bind to the resin and flows through the resin, and the undesired ADC species is bound to the resin. A flow through process may be performed in a single pass mode (where the ADC species of interest are obtained as a result of a single pass through the resin of the container) or in a multi-pass mode (where the ADC s of interest are obtained as a result of multiple passes h the resin of the container). The flow through process is performed such that the weight of resin selected binds to the undesired ADC population, and the desired ADCs (e.g., DAR 2-4) flow over the resin and are collected in the flow through after one or multiple passes.

In one embodiment of the invention, a flow through process may be used to t an ADC mixture comprising a drug loaded species of 4 or less and a drug loaded species of 6 or more with a hobic resin, wherein the amount of hydrophobic resin contacted with the ADC mixture is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant binding of the drug load species of 4 or less, where the drug load species of 4 or less passes over the resin and is uently collected after one or multiple passes, such that the composition comprising the desired ADCs (e.g. DAR 2-4) is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and n the ADC ses an antibody conjugated to an auristatin. In a te embodiment, a flow through process is used to contact an ADC mixture comprising a drug loaded species of 4 or less and a drug loaded species of 6 or more with a hydrophobic resin by passing the ADC mixture over the resin, wherein the amount of hydrophobic resin contacted with the ADC mixture is sufficient to allow binding of the drug loaded species of 6 or more to the resin but does not allow significant binding of the drug load species of 4 or less, where the drug load species of 4 or less passes over the resin and is subsequently collected, such that the composition comprising ADCs is obtained, wherein the composition comprises less than 15% of the drug loaded species of 6 or more, and wherein the ADC comprises an antibody ated to an auristatin, wherein the amount of hydrophobic resin weight is 3 to 12 times the weight of the drug loaded species of 6 or more in the ADC mixture.

Purification methods may be based on the use of a hydrophobic resin to separate high vs. low drug loaded species of ADC. Hydrophobic resin comprises hydrophobic groups which ct with the hydrophobic properties of the ADCs. Hydrophobic groups on the ADC interact with hydrophobic groups within the hobic resin. The more hobic a protein is the stronger it will interact with the hydrophobic resin.

Hydrophobic resin normally comprises a base matrix (e.g., cross-linked agarose or synthetic copolymer material) to which hydrophobic ligands (e.g., alkyl or aryl groups) are coupled. Many hydrophobic resins are available commercially. Examples include, but are not limited to, Phenyl SepharoseTM 6 Fast Flow with low or high substitution (Pharmacia LKB Biotechnology, AB, Sweden); Phenyl SepharoseTM High Performance (Pharmacia LKB Biotechnology, AB, Sweden); Octyl SepharoseTM High Performance (Pharmacia LKB Biotechnology, AB, Sweden); FractogelTM EMD Propyl or FractogelTM EMD Phenyl columns (E. Merck, Germany); Macro-PrepTM Methyl or Macro-PrepTM. t-Butyl Supports (Bio-Rad, California); WP HI-Propyl (C3)TM (J. T. Baker, New Jersey); and ToyopearlTM ether, hexyl, phenyl or butyl (TosoHaas, PA). In one embodiment, the hydrophobic resin is a butyl hydrophobic resin. In another embodiment, the hobic resin is a phenyl hydrophobic resin. In another embodiment, the hydrophobic resin is a hexyl hydrophobic resin, an octyl hydrophobic resin, or a decyl hobic resin. In one embodiment, the hydrophobic resin is a methacrylic polymer having n-butyl ligands (e.g. TOYOPEARL Butyl-600M).

Additional methods for purifying separate low and high DAR ADCs are disclosed in U.S. Provisional Application No. 61/792,834 and U.S. Application No. 14/210,602, filed on March 14, 2014 , the disclosures of which are incorporated by reference herein.

IV. Formulation Uses In accordance with the present methods, a ation comprising an GFR ADC is administered to a subject having (or at risk of ) a disorder requiring treatment with an anti-EGFR antibody or an anti-EGFR-ADC. The formulation comprising the anti- EGFR ADC may be administered either alone or in combination with other itions in the prevention or ent of the disorder requiring treatment with the anti-EGFR antibody.

As used herein, the term "a disorder in which EGFR activity is detrimental" is intended to include es and other disorders in which the presence of EGFR in a subject ing from the disorder has been shown to be or is suspected of being either responsible for the pathophysiology of the disorder or a factor that butes to a worsening of the disorder. Accordingly, a disorder in which EGFR activity is detrimental is a er in which inhibition of EGFR activity is expected to alleviate the symptoms and/or progression of the disorder. Such disorders may be evidenced, for e, by an increase in the activity of EGFR or an increase in the amount of EGFR present in a biological sample from a subject ing from the disorder (e.g., an increase in the concentration of EGFR in a tissue sample, in serum, plasma, synovial fluid, etc. of the subject), which can be detected, for example, using an anti-EGFR antibody.

The formulations of the invention may be used to treat cancer. Examples of cancer that may be d include, but are not limited to, glioblastoma, non-small cell lung cancer, lung , colon cancer, head and neck cancer, breast , squamous cell tumors, anal cancer, skin cancer, and vulvar .

In one embodiment, a formulation comprising an ADC1-MMAF may be administered to a t for the treatment of colorectal , head and neck cancer (including, but not limited to, hypopharyngeal cancer, oropharyngeal cancer, geal cancer, laryngeal cancer, and oral cavity cancer), pancreatic cancer, and gastric cancer. In one aspect of the ion, a formulation comprising an ADC1-MMAF is administered to a subject to treat a solid tumor likely to xpress the Epidermal Growth Factor Receptor (EGFR), squamous non-small cell lung cancer (NSCLC), or glioblastoma multiforme. Additional examples of such cancers that may be treated with the compositions of the invention include squamous tumors (including, squamous tumors of the lung, head and neck, cervical, etc.), glioblastoma, glioma, non-small cell lung cancer, lung cancer, colon cancer, head and neck cancer, breast cancer, squamous cell tumors, anal cancer, skin cancer, and vulvar .

The unique specificity of anti-EGFR ADCs provides diagnostic and therapeutic uses to identify, characterize, target and treat, reduce or ate a number of tumorigenic cell types and tumor types, for e, but not limited to, glioblastoma, non-small cell lung cancer, lung cancer, colon cancer, head and neck , breast cancer, squamous cell tumors, anal cancer, skin cancer and vulvar cancer, without the problems associated with normal tissue uptake that may be seen with previously known EGFR antibodies. Thus, cells overexpressing EGFR (e.g. by amplification or expression of a mutant or variant EGFR), and in particular embodiments, those demonstrating aberrant post-translational modification may be recognized, isolated, characterized, ed and treated or eliminated utilizing anti-EGFR ADCs.

In one aspect of the invention, there is provided a method for treating a subject comprising administering a therapeutically effective amount of an anti-EGFR ADC in any of the formulations as described herein, wherein the subject has a disorder requiring treatment with the anti-EGFR antibody in the formulation (e.g. a tumor, a cancerous condition, a precancerous condition, and any condition related to or resulting from hyperproliferative cell growth), such as, but not limited to, a solid tumor likely to over-express the Epidermal Growth Factor Receptor (EGFR) or glioblastoma multiforme.

Methods for detecting expression of EGFR in a tumor are known in the art, e.g., the EGFR pharmDx™ Kit (Dako). In contrast, an "EGFR negative tumor" is defined as a tumor having an absence of EGFR membrane staining above background in a tumor sample as determined by immunohistochemical techniques.

Formulations comprising anti-EGFR ADCs can thus specifically be used to categorize the nature of EGFR tumors or tumorigenic cells, by staining or otherwise recognizing those tumors or cells wherein EGFR overexpression, particularly ication and/or EGFR mutation, particularly de2-7 EGFR, is present. Further, anti-EGFR ADCs have been shown to demonstrate significant in vivo anti-tumor activity against tumors containing amplified EGFR and against de2-7 EGFR positive xenografts. ore, in a further aspect of the invention, there is provided a method of treatment of a tumor, a cancerous condition, a precancerous condition, and any ion related to or resulting from hyperproliferative cell growth comprising administration of an anti-EGFR ADC in a formulation bed herein.

Various delivery systems are known and can be used to administer formulations comprising GFR ADCs. s of introduction include but are not limited to intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral . The ADCs can be administered, for example by on or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, and the like) and can be administered together with other biologically active agents such as herapeutic agents. Administration can be systemic or local. In one embodiment, the formulation of the invention is delivered to a subject intravenously. In another embodiment, the formulation of the invention is red to a subject subcutaneously. In one ment, the t administers the formulation to himself/herself (self-administration).

The amount of the ADC that is effective in the treatment or prevention of a disorder requiring ent with the anti-EGFR ADC in the formulation, e.g. a cancer, can be determined by standard al techniques. In addition, in vitro assays may optionally be employed to help identify optimal dosage ranges. The e dose will also depend on the route of administration, and the stage of immunological disorder or EGFR-expressing cancer, and may be decided according to the judgment of the practitioner and each patient's circumstances. In one embodiment, a therapeutically effective amount of the anti-EGFR ADC in the formulation is administered to a subject in need thereof. The term "therapeutically effective amount" or "effective amount" of an anti-EGFR ADC, as used herein, refers to an amount effective in the prevention or treatment or alleviation of a symptom of a disorder for the treatment of which the ADC is effective. An example of a therapeutically effective amount of the anti-EGFR ADC in the formulation is an amount sufficient to inhibit detrimental EGFR activity or treat a disorder in which EGFR activity is detrimental.

A dose of an anti-EGFR ADC can be stered, for example, daily, once per week (weekly), twice per week, thrice per week, four times per week, five times per week, biweekly, every three weeks, monthly or every four weeks, or otherwise as needed.

In certain embodiments, In certain embodiments, the anti-EGFR ADC can be coadministered to a subject with one or more additional therapeutic agents to treat cancer. The term "co-administered" means the administration of two or more different pharmaceutical agents or treatments (e.g., radiation treatment) that are administered to a subject by combination in the same pharmaceutical composition or separate pharmaceutical compositions. Thus co-administration involves administration at the same time of a single pharmaceutical composition comprising two or more pharmaceutical agents or stration of two or more different compositions to the same subject at the same or different times.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, where es of the agents include, such as radiation, alkylating agents, angiogenesis inhibitors, dies, tabolites, antimitotics, antiproliferatives, antivirals, aurora kinase inhibitors, apoptosis promoters (for e, Bcl-xL, Bcl-w and Bfl-1) inhibitors, activators of death or pathway, Bcr-Abl kinase inhibitors, BiTE (Bi-Specific T cell Engager) antibodies, antibody drug conjugates, biologic response modifiers, cyclindependent kinase inhibitors, cell cycle inhibitors, cyclooxygenase-2 inhibitors, DVDs (dual variable domain antibodies), leukemia viral oncogene homolog ) receptor inhibitors, growth factor inhibitors, heat shock protein (HSP)-90 inhibitors, e deacetylase (HDAC) inhibitors, hormonal therapies, immunologicals, tors of inhibitors of apoptosis proteins (IAPs), intercalating antibiotics, kinase inhibitors, kinesin tors, Jak2 inhibitors, mammalian target of rapamycin inhibitors, microRNA’s, mitogen-activated extracellular signal-regulated kinase inhibitors, multivalent g proteins, non-steroidal anti-inflammatory drugs s), poly ADP (adenosine diphosphate)-ribose polymerase (PARP) inhibitors, platinum chemotherapeutics, polo-like kinase (Plk) inhibitors, phosphoinositide-3 kinase domain) tors, proteosome inhibitors, purine analogs, pyrimidine analogs, receptor tyrosine kinase inhibitors, etinoids/deltoids plant alkaloids, small inhibitory ribonucleic acids (siRNAs), topoisomerase inhibitors, ubiquitin ligase inhibitors, and the like, and in ation with one or more of these agents.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including BiTE antibodies, which are cific antibodies that direct T-cells to attack cancer cells by simultaneously binding the two cells. The T-cell then attacks the target cancer cell. es of BiTE antibodies include adecatumumab (Micromet MT201), blinatumomab met MT103) and the like. Without being limited by theory, one of the mechanisms by which T-cells elicit apoptosis of the target cancer cell is by osis of cytolytic granule components, which include perforin and me B. In this regard, Bcl-2 has been shown to attenuate the induction of apoptosis by both perforin and granzyme B.

These data suggest that inhibition of Bcl-2 could enhance the cytotoxic effects elicited by T- cells when targeted to cancer cells (V.R. Sutton, D.L. Vaux and J.A. Trapani, J. of Immunology 1997, 158 (12), 5783).

Anti-EGFR ADCs (or ations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including siRNA. SiRNAs are molecules having endogenous RNA bases or chemically modified tides. The modifications do not abolish cellular activity, but rather impart increased stability and/or increased cellular potency. Examples of chemical modifications include phosphorothioate groups, 2'-deoxynucleotide, 2'-OCH3-containing ribonucleotides, 2'-F-ribonucleotides, 2'-methoxyethyl ribonucleotides, combinations f and the like.

The siRNA can have varying lengths (e.g., 10-200 bps) and structures (e.g., hairpins, single/double strands, bulges, nicks/gaps, mismatches) and are processed in cells to provide active gene silencing. A -stranded siRNA (dsRNA) can have the same number of nucleotides on each strand (blunt ends) or asymmetric ends (overhangs). The overhang of 1-2 tides can be present on the sense and/or the antisense strand, as well as present on the '- and/ or the 3'-ends of a given strand.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a eutically effective amount of one or more agents to treat a cancer, including DVDs and other multivalent binding proteins. Multivalent g proteins are binding proteins comprising two or more antigen binding sites. Multivalent g proteins are engineered to have the three or more n binding sites and are generally not lly occurring antibodies. The term "multispecific binding protein" means a binding protein capable of binding two or more related or unrelated targets. Dual variable domain (DVD) binding proteins are tetravalent or multivalent binding proteins binding proteins comprising two or more antigen binding sites. Such DVDs may be monospecific (i.e., capable of g one antigen) or multispecific (i.e., capable of binding two or more antigens). DVD binding proteins comprising two heavy chain DVD ptides and two light chain DVD polypeptides are referred to as DVD Ig's. Each half of a DVD Ig comprises a heavy chain DVD polypeptide, a light chain DVD ptide, and two antigen binding sites. Each binding site comprises a heavy chain variable domain and a light chain variable domain with a total of 6 CDRs involved in antigen binding per antigen binding site. Multispecific DVDs include DVD binding proteins that bind DLL4 and VEGF, or C-met and EGFR or ErbB3 and EGFR.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a therapeutically effective amount of one or more agents to treat a cancer, including alkylating agents. Alkylating agents include altretamine, AMD-473, AP-5280, uone, bendamustine, brostallicin, busulfan, carboquone, carmustine (BCNU), chlorambucil, CLORETAZINE® (laromustine, VNP 40101M), cyclophosphamide, decarbazine, estramustine, fotemustine, glufosfamide, ifosfamide, KW-2170, lomustine (CCNU), mafosfamide, melphalan, mitobronitol, mitolactol, nimustine, en mustard e, ranimustine, temozolomide, thiotepa, TREANDA® (bendamustine), treosulfan, rofosfamide and the like.

Anti-EGFR ADCs (or formulations comprising GFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including angiogenesis inhibitors. Angiogenesis inhibitors e endothelial-specific receptor tyrosine kinase (Tie-2) inhibitors, epidermal growth factor receptor (EGFR) inhibitors, insulin growth factor-2 receptor 2) inhibitors, matrix metalloproteinase-2 (MMP-2) inhibitors, matrix metalloproteinase-9 (MMP-9) inhibitors, platelet-derived growth factor receptor (PDGFR) inhibitors, thrombospondin analogs, vascular endothelial growth factor receptor tyrosine kinase (VEGFR) inhibitors and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including antimetabolites. Antimetabolites include ALIMTA® (pemetrexed disodium, 14, MTA), 5-azacitidine, XELODA® (capecitabine), carmofur, LEUSTAT® (cladribine), abine, cytarabine, cytarabine ocfosfate, cytosine arabinoside, decitabine, xamine, doxifluridine, eflornithine, EICAR (5-ethynylβ -D-ribofuranosylimidazole- 4-carboxamide), enocitabine, ethnylcytidine, fludarabine, 5-fluorouracil alone or in combination with leucovorin, GEMZAR® (gemcitabine), hydroxyurea, ALKERAN®(melphalan), mercaptopurine, 6-mercaptopurine riboside, methotrexate, mycophenolic acid, nelarabine, nolatrexed, ocfosfate, pelitrexol, pentostatin, raltitrexed, Ribavirin, triapine, trimetrexate, S-1, tiazofurin, tegafur, TS-1, vidarabine, UFT and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including rals. Antivirals e ritonavir, ychloroquine and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including aurora kinase inhibitors. Aurora kinase inhibitors include ABT-348, 52, MLN-8054, , Aurora A-specific kinase inhibitors, Aurora B-specific kinase tors and pan-Aurora kinase inhibitors and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including Bcl-2 n inhibitors. Bcl-2 protein inhibitors include AT-101 ssypol), GENASENSE® (G3139 or oblimersen (Bcltargeting antisense oligonucleotide)), IPI-194, IPI-565, N-(4-(4-((4'-chloro(1,1'-biphenyl)yl)methyl)piperazinyl)benzoyl)(((1R) (dimethylamino)((phenylsulfanyl)methyl)propyl)amino)nitrobenzenesulfonamide) (ABT-737), N-(4-(4-((2-(4-chlorophenyl)-5,5-dimethylcyclohexen yl)methyl)piperazinyl)benzoyl)(((1R)(morpholinyl) ((phenylsulfanyl)methyl)propyl)amino)((trifluoromethyl)sulfonyl)benzenesulfonamide (ABT-263), GX-070 clax), ABT-199, and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a eutically ive amount of one or more agents to treat a cancer, including Bcr-Abl kinase inhibitors, such as DASATINIB® (BMS-354825), C® (imatinib) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a , including CDK inhibitors. CDK inhibitors include AZD-5438, BMI-1040, BMS-032, BMS- 387, 84, flavopyridol, 6199, MCS-5A, PD0332991, PHA-690509, seliciclib (CYC-202, R-roscovitine), ZK-304709 and the like.

Anti-EGFR ADCs (or ations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a , including COX-2 inhibitors. COX-2 inhibitors include ABT-963, ARCOXIA® (etoricoxib), BEXTRA® (valdecoxib), BMS347070, CELEBREX® (celecoxib), COX-189 acoxib), CT-3, DERAMAXX® (deracoxib), JTE-522, 4-methyl(3,4-dimethylphenyl)(4- oylphenyl-1H-pyrrole), MK-663 (etoricoxib), NS-398, parecoxib, RS-57067, SC-58125, SD-8381, SVT-2016, S-2474, T-614, VIOXX® (rofecoxib) and the like.

GFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- stered with a therapeutically effective amount of one or more agents to treat a cancer, including other EGFR inhibitors. EGFR inhibitors include EGFR antibodies, ABX-EGF, anti-EGFR immunoliposomes, ccine, EMD-7200, ERBITUX® (cetuximab), HR3, IgA antibodies, IRESSA® (gefitinib), TARCEVA® (erlotinib or OSI-774), TP-38, EGFR fusion protein, TYKERB® (lapatinib) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including HER2 inhibitors. ErbB2 receptor inhibitors include CP714, CI-1033 (canertinib), HERCEPTIN® (trastuzumab), TYKERB® (lapatinib), OMNITARG® (2C4, petuzumab), TAK-165, GW-572016 (ionafarnib), GW-282974, EKB-569, PI-166, dHER2 (HER2 vaccine), APC-8024 (HER-2 vaccine), anti-HER/2neu bispecific antibody, B7.her2IgG3, AS HER2 ctional bispecfic antibodies, mAB AR-209, mAB 2B-1 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including histone deacetylase inhibitors, such as depsipeptide, LAQ-824, MS-275, trapoxin, suberoylanilide amic acid (SAHA), TSA, valproic acid and the like.

HSP-90 inhibitors e 17-AAG-nab, 17-AAG, CNF-101, CNF-1010, CNF-2024, 17-DMAG, geldanamycin, IPI-504, KOS-953, MYCOGRAB® (human recombinant antibody to HSP-90), NCS-683664, PU24FCl, PU-3, radicicol, SNX-2112, STA-9090 09 and the like.

Anti-EGFR ADCs (or ations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including inhibitors of inhibitors of apoptosis proteins, such as HGS1029, GDC-0145, GDC- 0152, LCL-161, LBW-242 and the like.

Anti-EGFR ADCs (or formulations sing anti-EGFR ADCs) can be coadministered with a therapeutically ive amount of one or more agents to treat a cancer, including other ADCs, such as anti-CD22-MC-MMAF, anti-CD22-MC-MMAE, D22- MCC-DM1, CRvcMMAE, DC, MEDI-547, SGN-19Am SGN-35, SGN-75 ADCs and the like Anti-EGFR ADCs (or formulations comprising GFR ADCs) can be nistered with a therapeutically effective amount of one or more agents to treat a cancer, including activators of death receptor pathway, such as TRAIL, antibodies or other agents that target TRAIL or death receptors (e.g., DR4 and DR5) such as Apomab, conatumumab, ETR2-ST01, GDC0145, (lexatumumab), HGS-1029, LBY-135, PRO-1762 and trastuzumab.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a therapeutically effective amount of one or more agents to treat a cancer, including kinesin inhibitors, such as Eg5 inhibitors such as AZD4877, ARRY-520; CENPE inhibitors such as GSK923295A and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including JAK-2 inhibitors, such as CEP-701 (lesaurtinib), XL019 and INCB018424 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a therapeutically ive amount of one or more agents to treat a cancer, including MEK tors, such as ARRY-142886, ARRY-438162 PD-325901, PD-98059 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including mTOR tors, such as AP-23573, CCI-779, everolimus, RAD-001, cin, temsirolimus, ATP-competitive TORC1/TORC2 inhibitors, ing PI-103, PP242, PP30, Torin 1 and the like.

GFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including non-steroidal anti-inflammatory drugs (NSAIDs), such as AMIGESIC® (salsalate), DOLOBID® (diflunisal), MOTRIN® (ibuprofen), ORUDIS® (ketoprofen), RELAFEN® (nabumetone), FELDENE® (piroxicam), ibuprofen cream, ALEVE® xen) and NAPROSYN® (naproxen), VOLTAREN® (diclofenac), INDOCIN® (indomethacin), CLINORIL® (sulindac), TOLECTIN® (tolmetin), LODINE® (etodolac), TORADOL® (ketorolac), DAYPRO® (oxaprozin) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including PDGFR inhibitors, such as C-451, CP-673, CP-868596 and the like.

GFR ADCs (or ations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including platinum chemotherapeutics, such as cisplatin, ELOXATIN® (oxaliplatin) eptaplatin, lobaplatin, nedaplatin, ATIN® (carboplatin), satraplatin, picoplatin and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a therapeutically effective amount of one or more agents to treat a cancer, including polo-like kinase inhibitors, e.g., BI-2536 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a eutically effective amount of one or more agents to treat a cancer, including phosphoinositide-3 kinase (PI3K) inhibitors, such as nnin, LY294002, XL- 147, CAL-120, ONC-21, AEZS-127, ETP-45658, PX-866, GDC-0941, BGT226, BEZ235, XL765 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including thrombospondin analogs, such as ABT-510 (thrombospondin mimetic), 7, ABT-898 (thrombospondin-1 mimetic peptide), TSP-1 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including VEGFR inhibitors, such as AVASTIN® (bevacizumab), ABT-869, AEE-788, ANGIOZYME™ (a ribozyme that inhibits angiogenesis (Ribozyme Pharmaceuticals (Boulder, CO.) and Chiron, (Emeryville, CA)), axitinib (AG-13736), AZD-2171, CP-547,632, IM-862, MACUGEN (pegaptamib), NEXAVAR® (sorafenib, BAY43-9006), pazopanib (GW-786034), vatalanib (PTK-787, ZK-222584), SUTENT® (sunitinib, SU- , VEGF trap, ZACTIMA™ (vandetanib, ZD-6474), GA101, ofatumumab, ABT-806 (mAb-806), ErbB3 specific antibodies, BSG2 specific antibodies, DLL4 specific antibodies and C-met specific antibodies, and the like. Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co-administered with a therapeutically effective amount of one or more agents to treat a , including antibiotics, such as intercalating antibiotics aclarubicin, actinomycin D, cin, cin, adriamycin, BLENOXANE® (bleomycin), daunorubicin, CAELYX® or MYOCET® omal doxorubicin), elsamitrucin, cin, glarbuicin, ZAVEDOS® (idarubicin), cin C, bicin, zinostatin, peplomycin, bicin, rebeccamycin, amer, streptozocin, R® (valrubicin), zinostatin and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a therapeutically effective amount of one or more agents to treat a cancer, including topoisomerase inhibitors, such as aclarubicin, 9-aminocamptothecin, amonafide, amsacrine, becatecarin, belotecan, BN-80915, CAMPTOSAR® (irinotecan hydrochloride), camptothecin, CARDIOXANE® (dexrazoxine), diflomotecan, edotecarin, ELLENCE® or RUBICIN® (epirubicin), etoposide, exatecan, 10-hydroxycamptothecin, gimatecan, lurtotecan, mitoxantrone, orathecin, pirarbucin, pixantrone, rubitecan, sobuzoxane, SN-38, tafluposide, topotecan and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- stered with a therapeutically effective amount of one or more agents to treat a cancer, including therapeutic antibodies, such as AVASTIN® (bevacizumab), CD40-specific antibodies, chTNT-1/B, denosumab, ERBITUX® (cetuximab), HUMAX-CD4® (zanolimumab), IGF1R-specific antibodies, lintuzumab, PANOREX® (edrecolomab), RENCAREX® (WX G250), RITUXAN® (rituximab), ticilimumab, trastuzimab, CD20 antibodies types I and II and the like.

Anti-EGFR ADCs (or ations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including hormonal therapies, such as ARIMIDEX® (anastrozole), AROMASIN® (exemestane), arzoxifene, CASODEX® (bicalutamide), CETROTIDE® (cetrorelix), degarelix, deslorelin, DESOPAN® (trilostane), dexamethasone, DROGENIL® (flutamide), EVISTA® (raloxifene), AFEMA™ (fadrozole), ON® (toremifene), FASLODEX® (fulvestrant), FEMARA® (letrozole), formestane, orticoids, HECTOROL® (doxercalciferol), RENAGEL® amer carbonate), lasofoxifene, lide acetate, MEGACE® (megesterol), MIFEPREX® (mifepristone), NILANDRON™ amide), NOLVADEX® (tamoxifen citrate), PLENAXIS™ (abarelix), prednisone, PROPECIA® teride), rilostane, SUPREFACT® (buserelin), TRELSTAR® (luteinizing hormone releasing hormone (LHRH)), VANTAS® (Histrelin implant), VETORYL® (trilostane or modrastane), ZOLADEX® (fosrelin, goserelin) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including deltoids and retinoids, such as citol (EB1089, CB1093), lexacalcitrol (KH1060), fenretinide, PANRETIN® (aliretinoin), ATRAGEN® omal tretinoin), TIN® (bexarotene), LGD-1550 and the like.

Anti-EGFR ADCs (or formulations sing anti-EGFR ADCs) can be co- stered with a therapeutically effective amount of one or more agents to treat a cancer, ing PARP inhibitors, such as veliparib, olaparib, KU-59436, AZD-2281, AG-014699, BSI-201, , INO-1001, ONO-2231 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be nistered with a eutically effective amount of one or more agents to treat a cancer, including plant alkaloids, such as, but are not limited to, vincristine, vinblastine, vindesine, vinorelbine and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including proteasome inhibitors, such as VELCADE® (bortezomib), MG132, NPI-0052, PR-171 and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including immunologicals. Examples of immunologicals include interferons and other immune-enhancing agents. Interferons include interferon alpha, interferon 2a, eron alpha-2b, interferon beta, interferon gamma-1a, ACTIMMUNE® (interferon gamma-1b) or interferon gamma-n1, combinations thereof and the like. Other agents include ALFAFERONE®,(IFN-α), BAM-002 (oxidized hione), BEROMUN® (tasonermin), BEXXAR® (tositumomab), CAMPATH® (alemtuzumab), CTLA4 (cytotoxic lymphocyte antigen 4), decarbazine, denileukin, epratuzumab, GRANOCYTE® (lenograstim), an, leukocyte alpha interferon, imiquimod, 0 (anti-CTLA-4), melanoma vaccine, mitumomab, mostim, MYLOTARG™ (gemtuzumab ozogamicin), EN® (filgrastim), OncoVAC-CL, ® (oregovomab), pemtumomab (Y-muHMFG1), PROVENGE® (sipuleucel-T), sargaramostim, sizofilan, teceleukin, THERACYS® (Bacillus Calmette-Guerin), ubenimex, VIRULIZIN® (immunotherapeutic, Lorus Pharmaceuticals), Z- 100 (Specific Substance of Maruyama (SSM)), WF-10 (Tetrachlorodecaoxide ), PROLEUKIN® (aldesleukin), ZADAXIN® (thymalfasin), X® (daclizumab), ZEVALIN® (90Y-Ibritumomab tiuxetan) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including biological response modifiers, such as agents that modify defense mechanisms of living sms or biological responses, such as survival, growth or differentiation of tissue cells to direct them to have anti-tumor activity and include krestin, lentinan, sizofiran, picibanil PF-3512676 (CpG-8954), ex and the like.

GFR ADCs (or ations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, ing pyrimidine analogs, such as bine (ara C or Arabinoside C), cytosine arabinoside, doxifluridine, FLUDARA® (fludarabine), 5-FU (5-fluorouracil), idine, GEMZAR® (gemcitabine), TOMUDEX® (ratitrexed), TROXATYL™ (triacetyluridine troxacitabine) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- administered with a therapeutically effective amount of one or more agents to treat a cancer, including purine analogs, such as LANVIS® (thioguanine) and PURI-NETHOL® (mercaptopurine).

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically effective amount of one or more agents to treat a cancer, including antimitotic agents, such as batabulin, epothilone D (KOS-862), N-(2-((4- hydroxyphenyl)amino)pyridinyl)methoxybenzenesulfonamide, ixabepilone (BMS 247550), paclitaxel, TAXOTERE® (docetaxel), PNU100940 1), patupilone, 81 (larotaxel), vinflunine, ZK-EPO (synthetic epothilone) and the like.

Anti-EGFR ADCs (or formulations comprising anti-EGFR ADCs) can be co- stered with a therapeutically effective amount of one or more agents to treat a cancer, including ubiquitin ligase inhibitors, such as MDM2 inhibitors, such as nutlins, NEDD8 inhibitors such as MLN4924 and the like.

Compounds of this invention can also be used as radiosensitizers that e the efficacy of radiotherapy. Examples of radiotherapy include external beam radiotherapy, teletherapy, therapy and sealed, unsealed source radiotherapy and the like.

GFR ADCs (or formulations comprising anti-EGFR ADCs) can be coadministered with a therapeutically ive amount of one or more agents to treat a cancer, including chemotherapeutic agents such as ABRAXANE™ (ABI-007), ABT-100 (farnesyl transferase inhibitor), ADVEXIN® (Ad5CMV-p53 vaccine), ALTOCOR® or MEVACOR® tatin), AMPLIGEN® (poly I:poly C12U, a synthetic RNA), APTOSYN® (exisulind), AREDIA® (pamidronic acid), arglabin, L-asparaginase, atamestane (1-methyl-3,17-dione- ta-1,4-diene), AVAGE® (tazarotene), AVE-8062 (combreastatin derivative) BEC2 (mitumomab), cachectin or in (tumor necrosis factor), canvaxin (vaccine), CEAVAC® (cancer vaccine), CELEUK® (celmoleukin), CEPLENE® (histamine dihydrochloride), CERVARIX® (human papillomavirus vaccine), CHOP® (C: N® (cyclophosphamide); H: ADRIAMYCIN® (hydroxydoxorubicin); O: Vincristine IN®); P: sone), CYPAT™ terone acetate), statin A4P, DAB(389)EGF (catalytic and translocation domains of eria toxin fused via a His-Ala linker to human epidermal growth factor) or TransMID-107R™ (diphtheria ), dacarbazine, dactinomycin, 5,6-dimethylxanthenoneacetic acid (DMXAA), eniluracil, EVIZON™ (squalamine lactate), DIMERICINE® (T4N5 liposome lotion), discodermolide, DX-8951f (exatecan mesylate), enzastaurin, EPO906 (epithilone B), GARDASIL® (quadrivalent human papillomavirus (Types 6, 11, 16, 18) recombinant vaccine), GASTRIMMUNE®, GENASENSE®, GMK (ganglioside conjugate vaccine), GVAX® (prostate cancer vaccine), halofuginone, histerelin, hydroxycarbamide, ibandronic acid, IGN- 101, ILPE38, ILPE38QQR (cintredekin besudotox), pseudomonas exotoxin, interferon-α, eron-γ, JUNOVAN™ or MEPACT™ (mifamurtide), lonafarnib, 5,10- methylenetetrahydrofolate, miltefosine (hexadecylphosphocholine), NEOVASTAT®(AE- 941), XIN® (trimetrexate onate), NIPENT® statin), ONCONASE® (a ribonuclease enzyme), ONCOPHAGE® (melanoma vaccine treatment), ONCOVAX® (IL-2 Vaccine), ORATHECIN™ (rubitecan), OSIDEM® (antibody-based cell drug), OVAREX® MAb (murine monoclonal antibody), paclitaxel, PANDIMEX™ (aglycone saponins from g comprising 20(S)protopanaxadiol (aPPD) and 20(S)protopanaxatriol (aPPT)), panitumumab, PANVAC®-VF (investigational cancer vaccine), pegaspargase, PEG Interferon A, phenoxodiol, procarbazine, rebimastat, REMOVAB® (catumaxomab), REVLIMID® (lenalidomide), RSR13 (efaproxiral), SOMATULINE® LA (lanreotide), SORIATANE® (acitretin), staurosporine (Streptomyces staurospores), talabostat (PT100), TARGRETIN® (bexarotene), TAXOPREXIN® aclitaxel), TELCYTA® (canfosfamide, TLK286), temilifene, TEMODAR® (temozolomide), tesmilifene, thalidomide, THERATOPE® (STn-KLH), thymitaq (2-amino-3,4-dihydromethyloxo(4- pyridylthio)quinazoline ochloride), TNFERADE™ (adenovector: DNA carrier containing the gene for tumor necrosis factor-α), TRACLEER® or ZAVESCA® (bosentan), tretinoin (Retin-A), tetrandrine, TRISENOX® (arsenic de), VIRULIZIN®, ukrain (derivative of alkaloids from the greater ine plant), vitaxin (anti-alphavbeta3 antibody), XCYTRIN® (motexafin gadolinium), XINLAY™ (atrasentan), XYOTAX™ (paclitaxel poliglumex), YONDELIS® (trabectedin), ZD-6126, ZINECARD® (dexrazoxane), ZOMETA® (zolendronic acid), zorubicin and the like.

In one ment, the formulation comprising the anti-EGFR-ADC is intravenously administered to a subject having glioblastoma in combination with radiation and/or TEMODAR® olomide).

Further, in one embodiment, the formulation can be provided as a ceutical kit comprising (a) a container containing an anti-EGFR ADC in lyophilized form and (b) a second container containing a pharmaceutically acceptable diluent (e.g., sterile water) for injection. The ceutically able diluent can be used for reconstitution or dilution of the lized ADC. Optionally associated with such container(s) can be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration.

The invention is further bed in the following examples, which are in not intended to limit the scope of the invention.

EXAMPLES Example 1: Stability Testing of dy Drug Conjugates (ADCs) The following example describes tests used to assay the stability of certain ADCs (in liquid form) in ison to ugated antibodies. Antibodies conjugated to either MMAF (see Figure 2) (referred to below as "ADC 1- MMAF" which is humanized anti- EGFR antibody 1- MMAF conjugate) or MMAE (see Figure 1) (referred to below as "ADC 1- MMAE" which is humanized anti-EGFR antibody 1 -MMAE conjugate) were tested and compared to humanized anti-EGFR antibody 1 alone. Among the properties examined were the onset of unfolding temperature using dynamic scanning fluorescence and DSC, secondary and tertiary ure analysis by FTIR and near UV-CD, respectively, accelerated stability at low and high concentrations, serum stability, freeze/thaw stability at low and high concentrations and solubility. The formulations described in this example were liquid formulations.

Analysis of onset of unfolding using Dynamic Scanning Fluorescence (DSF) and Differential Scanning Calorimetry (DSC) Two different techniques, dynamic scanning fluorescence (DSF) and ential scanning calorimetry (DSC), were used to determine the onset of unfolding and the conformational stability of antibody 1, ADC 1- MMAF and ADC 1- MMAE during thermal denaturation. As shown in Figure 3A, the change in scence intensity was related to protein unfolding levels and temperatures. The results from thermostability ements were compared with the data acquired using DSC (Figure 3B). Unfolding of the protein at a temperature greater than 55º C was used as a measure of stability. As shown in Figure 3A and B, the onset of unfolding occurred at a lower ature in ADC 1- MMAE (46º C) compared to ADC 1- MMAF (55º C), and was highest for antibody 1 (61º C), indicating antibody 1 was the most stable of the three molecules. Thus, the ADCs showed thermodynamic stability se, as was reflected in the lower unfolding temperatures for ADC 1- MMAF and ADC-1 MMAE vs. antibody 1 alone. ary and tertiary structure es of antibody 1, ADC 1- MMAF and ADC 1-MMAE The stabilities of antibody 1 , ADC 1- MMAF, and ADC 1-MMAE were determined using both Fourier Transform Infrared Spectroscopy (FTIR) and near UV- Circular Dichroism (CD). It has been shown that CD spectra between 260 and imately 180 nm can be analyzed for the ent secondary ural types: alpha helix, parallel and antiparallel beta sheet, turn, and other. Changes in secondary structure of antibody 1, the ADC 1- MMAF and ADC 1-MMAE in citrate / phosphate buffer alone at pH 5/6/7 were monitored by FTIR (Figure 4A) and CD (Figure 4B). As shown in Figures 4A and 4B, physical characteristics of ADC 1- MMAE and ADC 1- MMAF were slightly altered in unstructured elements compared to antibody 1. There were also ly altered unstructured elements in ADC 1- MMAE and ADC 1- MMAF compared to antibody 1 alone, as evidenced by the FTIR data in Figure 4A. In general, however, each of the three molecules showed the presence of > 40% β sheet band at 1638 cm-1. CD results showed a different profile for ADC 1- MMAE as compared to ADC 1- MMAF and antibody 1 (Figure 4B).

Generally, however, each of the les had an S-shaped profile with negative ellipticity at 280 nm. rated stability studies of dy 1, ADC 1- MMAF and ADC 1-MMAE Accelerated stability studies can help provide information on the effect of short term exposure to conditions that otherwise typically occur over a longer period. Antibody 1, ADC 1- MMAF and ADC 1- MMAE were formulated at both low concentrations (1 mg/ml) in 10 mM citrate/ phosphate buffer, pH 6, and higher concentrations (60 mg/ml) in 15 mM histidine, pH 5.75. Stability was defined as less than 5% monomer loss at 40ºC after 7 days at most stable pH The results of these studies are shown in Figure 5 and Figure 6. Figure 5 shows aggregation (as % aggregates; determined by SEC analysis) at an initial time point (T0), and after storage at 40ºC for 7 days. Figure 5 shows that at a concentration of 1 mg/ml, there was an increased aggregation propensity of ADC 1- MMAE at low concentrations, compared to ADC 1- MMAF and antibody 1. Figure 6 shows aggregation (as % aggregates) at initial time point (T0), and after storage at 40 C for 7 days. Figure 6 shows that at a concentration of 60 mg/ml, there is a significantly increased aggregation propensity of ADC 1-MMAE at high concentrations, as compared to ADC 1- MMAF and antibody 1. r, there was no impact of known stabilizing agents like hydroxy propyl beta cyclodextrin (labeled " in "Figure 6) on aggregation.

Plasma ity of antibody 1, ADC 1-MMAF and ADC 1-MMAE Plasma stability plays an important role in drug discovery and development, as unstable nds tend to have rapid clearance and short half-life, resulting in poor in vivo performance. The in vitro serum stability of antibody 1, ADC 1- MMAF and ADC 1-MMAE was evaluated in a serum stability assay. Briefly, the antibodies were labeled with Aexa Flur® (Life Technologies). Labeled antibody 1 and ADCMMAF and ADCMMAE were then incubated in filtered serum. Samples were collected on days 0, 1, 3, 5, 7, and analyzed by xclusion chromatography (SEC). The slope of the percent of high molecular weight (HMW) aggregates was calculated between days 0-7. ity was defined as less than 1% HMW species per day. Thus, the lower the slope, the less aggregation was present. More specifically, the graph in Figure 7 shows that the slope of the ADC 1-MMAF (0.5%) was lower than antibody 1 (1.10%) and ADC 1-MMAE (2.30), thus, ting less aggregation and better plasma stability. Figure 7 also describes the slopes of the percent of HMW aggregates for a range of other molecules, e.g., antibodies and DVD-Igs, for comparison purposes. /thaw stability of high and low concentrations of antibody 1, ADC 1-MMAF and ADC 1--MMAE Aggregation of antibodies can be induced by freeze-thawing and ed temperature, typical stress factors during development, production and storage. Antibody 1, ADC 1- MMAF and ADC 1- MMAE were subjected to 0, 1 or 2 freeze-thaw cycles, and characterized by spectroscopic techniques (SEC). High concentrations of antibody 1 (210 mg/ml), ADC 1- MMAF (135 mg/ml) and ADC 1-MMAE (145 mg/ml) were formulated in mM histidine buffer at a pH of 5.75. The results showing the % r (determined by SEC) are bed in Figure 8A, and suggest that there was no change in aggregation (defined as < 2% HMW species increase after 2 F/T cycles) among the three molecules In the experiments shown in Figure 8B, antibody 1, ADC 1-MMAF and ADC 1-MMAE at the same concentrations were formulated at a concentration of 1 mg/ml in 10 mM citrate and 10 mM phosphate buffer at a pH of 7.0. As shown in Figures 8A and 8B, there was no significant change in freeze/thaw stability after one or two cycles of freeze/ thaw among antibody 1, ADC 1-MMAF and ADC 1-MMAE at either high or low concentrations.

Particle formation was also tested for the three molecules at a concentration of 1 mg/ml in citrate / ate buffer alone at pH 6, during freeze-thawing (0, 1 or 2 freeze thaw ). ible particles (>= 10 µm and >= 25 µm, respectively) were determined to be below pharmacopeial limits (>= 10 µm and less than or equal to 600/ Ml (>= 25 µm), tively (Figure 9A). Microflow imaging (MFI) was also used to detect and quantify subvisible particles (less than 10 microns) e 9B). Figures 9A and 9B describe an overall increase in subvisible particles for antibody 1, ADC 1-MMAF and ADC 1-MMAE over time.

Solubility of antibody 1 versus ADC 1 with MMAF or MMAE The solubility of antibody 1, ADC 1-MMAF and ADC 1-MMAE in a formulation containing 10 mM citrate and 10 mM phosphate buffer system at pH 6 was examined at 5 degrees C. Solubility was defined as a on having no precipitate when formulated at at least a concentration of 50 mg/ml. The solubility of each of antibody 1, ADC 1- MMAF and ADC 1-MMAE was determined to be as follows: antibody 1 > 210 mg/mL; ADC 1-MMAF : > 135 mg/mL (Source 1); ADC 1-MMAF : > 92 mg/mL A(Source 2); ADC 1-MMAE: > 145 mg/mL (Source 1); and ADC : > 116 mg/mL (Source 2). It is noted that solubility may have ed the above mentioned concentrations, as limited material prevented further concentration.

Conclusion Overall, ADC 1-MMAF and ADC1-MMAE showed lower ity than unconjugated dy 1, as described, for example, in the accelerated studies and the unfolding assay described herein.

Example 2: ADC 1-MMAF Stable Lyophilized ation ADC 1-MMAF is an anti-EGFR antibody drug conjugate comprising antibody 1 covalently linked to MMAF. ADC 1-MMAF was ated as a lyophilized powder for injection upon reconstitution and packaged in glass vials. The lyophilized powder was reconstituted with 5 mL sterile water for injection (SWFI) and provided a 20 mg/mL of ADC 1-MMAF solution for injection. The drug product ation was for single use and contained no preservative. The composition of the ADC 1-MMAF per vial (lyophilized powder) and per mL (reconstituted solution) is described in Table 1, below. The reconstituted drug product was diluted with 0.9% saline solution (Sodium Chloride Injection, USP) for dose administration by infusion.

Table 1. ition of ADC 1-MMAF Powder for Injection Solution, 20 mg/mL Amount (mg) Amount (mg/mL) Name of Ingredients Function per vial reconstituted ADC 1-MMAF Drug substance 105 20 Histidine Buffering agent 12 2.3 e Bulking agent 368 70 Polysorbate 80 tant 0.53 0.10 Hydrochloric acid a pH adjustment q.s. q.s.

Water for Injection/ Vehicle Not applicable b To total weight of Water for injections 1032 mg a. Used as 10% solution b. Not present after freeze drying The formulation described in Table 1 is representative of a lyophilized formulation for an anti-EGFR ADC where the conjugate is an auristatin derivative, such as MMAF. The formulation comprises a buffer, a sugar, a surfactant and an anti-EGFR antibody drug conjugate. es 3-5 describe stability studies testing the lyophilized ADC 1-MMAF formulation described in Example 2. Examples 6-8 describe stability studies testing the purified lyophilized ADC 1-MMAF formulation described in e 2. For stability studies, ADC 1-MMAF (or ADC1-MMAFp) was stored as a lyophilizate in 20 ml colorless glass vials, closed with grey rubber stopper and a grey plastic cap. ADC 1-MMAF (or ADC1-MMAFp) was stored under the ing three separate conditions: 5º C; 25º C (60% relative humidity); 40º C (75% relative ty) for stability testing.

Example 3: ity of ADC 1-MMAF in a Lyophilized Formulation at 5º C The following experiments were performed after reconstitution with SWFI at the initial time point, and after reconstitution following storage of the lyophilizate for up to eighteen months at 5º C.

Appearance of lyophilizate and reconstituted solution not ed by long term storage at 5º C Appearance of the lyophilizate and of the reconstituted solution was visually assessed to confirm that the lyophilizate was practically free from visible foreign particulate matter and free from moisture in packaging material. At the initial time point, and after reconstitution following storage at 5º C for up to twelve months, the appearance of the lyophilizate complied with the ing criteria. After titution following storage at 5º C for up to twelve months, the reconstituted solution was a colorless to slightly yellow solution, and was practically free from visible particulate .

Color of solution not impacted by long term storage at 5º C Color of the reconstituted solution (visual) was assessed using a Blue / Yellow scale (BY-scale), where the samples were tested against a reference solution and the values reported. At the initial time point, and after reconstitution following e at 5º C for up to twelve months, all tituted ons had a BY-scale measure less than or equal to 7.

Thus, storage did not affect the color of the solution.

Clarity and opalescence of solution not affected by long term storage at 5º C Clarity and opalescence of the reconstituted solution was measured by a standard ometer using the light scattering ple and followed the respective Ph. Eur. or USP methods (as was also done for Examples 4 to 8). At the initial time point, and after reconstitution following storage at 5º C for up to twelve months, the appearance of the reconstituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, ph. Eur) (< = RSII).

Protein content of solution not affected by long term storage at 5º C Protein content of the reconstituted solution was determined. The protein concentration of the ADC was ined spectrophotometrically using a wavelength of 280 nm and the MAF extinction coefficient (1.43) (as was also done for Examples 4 to 8). At the initial time point, protein content of the reconstituted solution was 18.8 mg/ml.

After reconstitution following storage at 5º C for three months, the protein content of the reconstituted solution was 20.2 mg/ml.

Biological activity of on not affected by long term storage at 5º C A cytotoxicity assay using a human epidermoid carcinoma cell line was used to test the biological activity (%) of the reconstituted solution in comparison to an ADC1-MMAF control which had been previously confirmed to have cytotoxic activity (the control having 100% activity). At the initial time point, relative biological activity was 109%. After reconstitution ing storage at 5º C for one month, relative biological activity was 105%.

After reconstitution following storage at 5º C for three , relative biological activity was 97%. After reconstitution following storage at 5º C for six months, relative biological activity was 108%. After reconstitution following storage at 5º C for nine months, relative biological activity was 105%. After reconstitution following storage at 5º C for 12 months, relative biological ty was 99%. After reconstitution following storage at 5º C for 18 months, relative biological activity was 112%.

Size of molecules and/or molecular complexes not affected by long term storage at 5º C Size exclusion chromatography of the reconstituted solution was performed using Size Exclusion-High mance Liquid Chromatography (SE-HPLC). SE-HPLC determined the purity of ADC1-MMAF using size-exclusion HPLC. The macromolecules are isocratically ted during the gel filtration HPLC according to the decreasing molecular size. Purity was determined by comparing the area of ADC1-MMAF main peak to the total area of the sample chromatogram, excluding buffer-related peaks. The method is capable of resolving high molecular weight aggregates and truncated dy species from the ADC1-MMAF main peak. This method was also used in Examples 4 to 8.

The main peak (%) was measured in addition to high molecular weight s (%) and low molecular weight species (%). At the initial time point, the main peak was 98.9%.

High lar weight species were 0.9% and low lar weight species were 0.2%.

After reconstitution following storage at 5º C for one month, the main peak was 98.8%. High molecular weight species were 0.9% and low molecular weight species were 0.2%.

After reconstitution following storage at 5º C for three months, the main peak was 98.8%. High molecular weight species were 1.0% and low lar weight species were 0.2%.

After reconstitution following storage at 5º C for six months, the main peak was 99.0%. High molecular weight species were 0.9% and low molecular weight species were 0.2%. \ After reconstitution following storage at 5º C for nine months, the main peak was 98.9%. High molecular weight species were 0.9% and low molecular weight species were 0.3%.

After reconstitution ing storage at 5º C for 12 months, the main peak was 98.8%. High molecular weight species were 0.8% and low lar weight s were 0.4%.

After reconstitution following storage at 5º C for 18 months, the main peak was 98.8%. High molecular weight species were 0.9% and low molecular weight species were 0.3%.

Thus, all time points showed little to no change in the main peak % and high and low molecular weight species among the initial, one, three, six, nine, twelve and eighteen month time point measurements.

Chromatographic peak of the solution unchanged by long term storage at 5º C Cation exchange chromatography (CEX) was performed on the reconstituted solution using High Performance Liquid Chromatography (CEX-HPLC). In cation exchange chromatography, positively d molecules are attracted to a negatively d solid support. The cation exchange (CEX-HPLC) chromatography assay is a charged based separation method which was used to monitor ity of ADC1-MMAF in test samples through comparison with a reference standard (ADC1-MMAF which had been previously terized). The method is capable of resolving the main peak from acidic and basic At the initial time point, and after reconstitution following storage at 5º C for up to eighteen months the appearance of the reconstituted on was characterized by a predominant chromatographic peak pattern of the sample that conformed to that of a control which was the MAF which had been previously characterized. Thus, the chromatographic peak remained relatively unchanged over the course of eighteen months at 5º C. 30 Purity of the solution not affected by long term storage at 5º C Capillary gel ophoresis (CE-SDS-R) was performed on the reconstituted solution at the initial time point, and after reconstitution following storage at 5º C for up to 18 months to determine the purity of the solution. At the initial time point, the percent purity was 97.4%. After reconstitution following storage at 5º C for one month, the percent purity was 97.6%. After reconstitution following storage at 5º C for three months, the percent purity was 96.9%. After reconstitution ing storage at 5º C for six months, the percent purity was 97.1%. After reconstitution following e at 5º C for nine months, the percent purity was 96.7%. After reconstitution following storage at 5º C for twelve months, the percent purity was 97.2%. After reconstitution following storage at 5º C for eighteen months, the percent purity was 97.3%. Thus, the purity of the reconstituted solution did not icantly change n the initial time point, and up to eighteen months after reconstitution.

Drug to antibody ratio of the solution unchanged after long term storage at 5º C hobic ction chromatography (HIC) was med on the tituted solution in order to determine the drug to antibody ratio (DAR) over the eighteen month time period. HIC is used to separate proteins on the basis of relative hydrophobicity. The HIC method is a measure of the hydrophobicity of ADC1-MMAF. The bound components are eluted off the ligand in order of increasing hydrophobicity by using a gradient to decrease the salt concentration of the mobile phase. For ADC1-MMAF, the first peak eluted from the column was unconjugated antibody. The remaining peaks ented an increasing number of drug-linker molecules per antibody. Thus, the number of drug-linkers per antibody was determined by peak retention time and relative peak area. This method was also used in Examples 4 to 8. At the initial time point, and after reconstitution following storage at 5º C for up to eighteen months, the drug to antibody ratio (DAR) was measured as 4.1-4.2 for all reconstituted solutions.

Percent unconjugated dy in the on unchanged after long term storage at 5º C The reconstituted solution was also analyzed to determine the percent unconjugated antibody for ADC1-MMAF using the HIC method described above for determining the DAR (and also used for Examples 4 to 8). At the initial time point, the percent was not more than 4.1. After reconstitution following storage at 5º C for one month, the percent was not more than 4.1. After reconstitution following storage at 5º C for three months, the percent was not more than 4.1. After titution following storage at 5º C for six months, the percent was not more than 3.9. After reconstitution following storage at 5º C for nine months, the percent was not more than 4.0. After reconstitution ing storage at 5º C for twelve months, the percent was not more than 4.0. After reconstitution following storage at 5º C for en months, the percent was not more than 4.0. Thus, the t at all times points was similar.

Percent quenched drug linker in the solution not changed by long-term storage at 5º C Reversed phase chromatography (RP-HPLC) was performed on the reconstituted solution to determine the percent quenched drug linker. RP-HPLC is the separation of molecules based upon their interaction with a hydrophobic matrix which is largely based on their polarity. This method ines the quantity of the quenched drug-linker, and total ties in the solution. ADC1-MMAF was removed from the sample by precipitation with methanol followed by centrifugation. The is of the supernatant for the quenched drug-linker and total ties was performed by RP-HPLC using a C-18 column with UV detection at 214 nm. This method was also used in Examples 4 to 8.

At the initial time point, the percent was not more than 0.007. After reconstitution following storage at 5º C for one month, the percent was not more than 0.005. After reconstitution following storage at 5º C for three months, the percent was not more than 0.006. After reconstitution following storage at 5º C for six months, the percent was not more than 0.005. After reconstitution following storage at 5º C for nine , the percent was not more than 0.005. After reconstitution following storage at 5º C for twelve , the percent was not more than 0.007. After reconstitution ing storage at 5º C for eighteen months, the percent was not more than 0.005. Thus, the percent at all times points was similar for percent quenched drug linker.

Total impurities in the solution did not change after long term storage at 5º C The reconstituted solution was also ed to ine the percent of total impurities using RP-HPLC, using the method described above with respect to the percent quenched linker (also used for Examples 4 to 8). At the initial time point, the percent was not more than 0.007. After reconstitution following storage at 5º C for one month, the percent was not more than 0.005. After reconstitution following storage at 5º C for three months, the percent was not more than 0.006. After reconstitution following storage at 5º C for six months, the percent was not more than 0.005. After reconstitution following e at 5º C for nine months, the percent was not more than 0.005. After reconstitution following storage at 5º C for twelve months, the percent was not more than 0.007. After reconstitution ing storage at 5º C for eighteen months, the percent was not more than 0.005. Thus, the percent at all times points was r for total impurities.

Particulate contamination of the solution not affected by long term storage at 5º C Particulate contamination was assessed by determining sub-visible particles.

Acceptance criteria was met by ining the number of particles r than 10 µm per container, with not more than 6000 (USP (US Pharmacopeia) and European Pharmacopoeia standard). At the initial time point, the number of particles per container greater than 10 µm was 33. After reconstitution following storage at 5º C for one month, the number of particles per container greater than 10 µm was 22. After reconstitution following storage at 5º C for three months, the number of particles per container greater than 10 µm was 25. After reconstitution following storage at 5º C for six months, the number of particles per container greater than 10 µm was 73. After reconstitution following storage at 5º C for twelve , the number of particles per container greater than 10 µm was 20. Thus, all time points met with the acceptance criteria for the number of particles per container greater than 10 µm.

Acceptance criteria was also met by determining the number of particles greater than µm per container, with NMT of 600 (USP (US copeia) and European Pharmacopoeia rd). At the initial time point, the number of particles per container greater than 25 µm was 0. After reconstitution following storage at 5º C for one month, the number of particles per container greater than 25 µm was 2. After reconstitution following storage at 5º C for three months, the number of les per ner r than 25 µm was 2. After reconstitution following storage at 5º C for six months, the number of particles per container greater than 25 µm was 10. After reconstitution following storage at 5º C for twelve months, the number of particles per ner greater than 25 µm was 3. Thus, all time points met with the acceptance criteria for the number of particles per container greater than 25 µm.

Water content of the solution not ed by long term storage at 5º C Water content was assessed by Karl-Fischer-Titration. Karl Fischer titration uses etric or volumetric titration to determine trace amounts of water in a , reported as a percent. At the initial time point, the percent water in the reconstituted solution was 2.0%. After titution following storage at 5º C for three months, the percent water in the reconstituted solution was 0.7%. After reconstitution following storage at 5º C for six months, the percent water in the reconstituted solution was 0.7%. After reconstitution following storage at 5º C for twelve months, the percent water in the reconstituted solution was 0.8%. Thus, at the initial time point, and after reconstitution following storage at 5º C for one, three, six and twelve months, the water content of the reconstituted solution was negligible. pH of the solution not ed by long term storage at 5º C pH of the reconstituted solution was determined at the initial time point, and after reconstitution following storage at 5º C for one, three, six and twelve months. At the initial time point, the pH value of the reconstituted solution was 6.0. After storage at 5º C for three months, the pH value of the reconstituted solution was 5.9. After storage at 5º C for six months, the pH value of the reconstituted solution was 5.9. After storage at 5º C for twelve , the pH value of the reconstituted solution was 5.9.

Osmolality of the on was not affected by long term storage at 5º C Osmolality of the reconstituted solution was determined at the initial time point, and after reconstitution following storage at 5º C for one month by measuring the mean value of milliosmoles of solute per kilogram of solvent (mOsmol/kg). At the initial time point, osmolality was 235 mOsmol/kg. At one month, osmolality was 251 /kg.

Example 4: Stability of ADC 1-MMAF in a Lyophilized Formulation at 25º C The following tests were med after reconstitution with SWFI at the initial time point, and after reconstitution ing e of the lyophilizate for one, three and six months at 25º C (60% relative humidity): Appearance of lyophilizate and reconstituted solution not impacted by long term storage at 25º C Appearance of the lyophilizate and of the reconstituted solution was visually assessed to confirm lyophilizate was practically free from visible foreign particulate matter and free from moisture in packaging material. At the initial time point, and after reconstitution following storage for one, three and six months at 25º C (60% relative humidity), the appearance of the lyophilizate complied with the foregoing criteria. After reconstitution, the reconstituted solution was a colorless to slightly yellow solution, practically free from visible particulate matter. Thus, at the initial time point, and after reconstitution ing storage for one, three and six months at 25º C (60% relative ty), the appearance of the reconstituted solution was that the solution was colorless to slightly yellow on, cally free from visible particulate matter.

Color of solution not impacted by long term storage at 25º C Color of solution (visual) was assessed using a Blue/Yellow (BY)-scale where the samples were tested t a reference solution and the values were reported. At the initial time point, and after titution following storage for one, three and six months at 25º C (60% relative humidity), all reconstituted solutions had a BY-scale measure less than or equal to 7. Thus, storage did not affect the color of the solution.

Clarity and opalescence of solution not affected by long term storage at 25º C Clarity and opalescence of the reconstituted solution was assessed. Acceptance criteria of the reconstituted solution was met if the reconstituted solution was not more opalescent than nce suspension IV (per European Pharmacopeia, ph. Eur.). At the initial time point, and after reconstitution following storage for one, three and six months at 25º C (60% ve humidity), the ance of the reconstituted solution was not more opalescent than nce suspension IV (per European Pharmacopeia, ph. Eur.) (< = RSII).

Biological ty of solution not affected by long term storage at 25º C A cytotoxicity assay using a human epidermoid carcinoma cell line was used to test the biological activity (%) of the reconstituted solution in comparison to an ADC1-MMAF control which had been usly confirmed to have xic activity (the control having 100% activity. At the initial time point, relative ical activity was 109%. After reconstitution following storage at 25º C (60% relative humidity) for one month, relative biological activity was 113%. After reconstitution following storage at 25º C/ 60% relative humidity for three months, relative biological activity was 103%. After reconstitution following storage at 25º C/ 60% relative humidity for six months, relative biological activity was 109%.

Size of les and/ or molecular complexes not affected by long term storage at 25º C Size exclusion chromatograph was performed by Size Exclusion-High Performance Liquid Chromatography (SE-HPLC). The main peak (%) was measured, in addition to high molecular weight s (%) and low molecular weight s (%). At the initial time point, the main peak was 98.9%. High molecular weight species were 0.9% and low molecular weight species were 0.2%. After reconstitution following storage for at 25º C (60% relative humidity) one month, the main peak was 98.8%. High molecular weight species were 1.0% and low molecular weight species were 0.2%. After reconstitution ing storage at 25º C (60% relative humidity) for three , the main peak was 98.8%. High molecular weight species were 1.0% and low molecular weight species were 0.2%. After reconstitution following storage at 25º C (60% relative humidity) for six months, the main peak was 98.9%. High molecular weight species were 0.9% and low molecular weight species were 0.2%. Thus, there was little to no change in main peak % and high and low molecular weight species among initial, one, three and six month measurements.

Chromatographic peak of the on unchanged by long term storage at 25º C Cation exchange tography (CEX) was performed by High Performance Liquid Chromatography (CEX-HPLC). At the initial time point, and after titution following storage at 25º C/ 60% relative humidity for one month, three months and six months the appearance of the reconstituted solution was characterized by a predominant chromatographic peak pattern of the sample that med to that of a reference standard.

Purity of the on not affected by long term storage at 25º C Capillary gel electrophoresis (CE-SDS-R) was performed on the reconstituted solution at the initial time point, and after reconstitution following e for one, three and six months at 25º C (60% relative humidity). At the initial time point, the percent purity was 97.4%. After reconstitution following e for one month, the t purity was 97.4%.

After reconstitution following storage for three months, the percent purity was 96.9%. After reconstitution following storage for six months, the percent purity was 97.1%. Thus, the purity of the reconstituted solution did not significantly change n the initial time point, and at and after reconstitution following storage for one, three and six months at 25º C (60% relative ty).

Drug to antibody ratio of the solution unchanged after long term storage at 25º C Hydrophobic interaction chromatography (HIC) was performed on the reconstituted solution. At the initial time point, and after reconstitution following storage for one, three and six months at 25º C (60% relative humidity), DAR was measured as 4.2 for all reconstituted solutions.

Percent unconjugated antibody in the solution unchanged after long term storage The reconstituted solution was analyzed to determine the percent unconjugated antibody. At the l time point, the percent was not more than 4.1. After reconstitution following storage for one month at 25º C (60% relative humidity), the percent was not more than 4.1. After reconstitution following storage for three months at 25º C (60% relative humidity), the percent was not more than 4.1. After reconstitution ing storage for six months at 25º C (60% ve humidity), the percent was not more than 3.9.

Percent quenched drug linker in the solution not changed by long-term storage at 25º C Reversed phase tography (RP-HPLC) was performed on the reconstituted solution to determine the percent quenched linker. At the initial time point, the percent was not more than 0.007. After reconstitution following storage for one month at 25º C (60% relative humidity), the percent was not more than 0.005. After reconstitution following storage for three months at 25º C (60% relative humidity), the percent was not more than 0.006. After titution following storage for six months at 25º C (60% relative humidity), the t was not more than 0.005. Thus, the percent at all times points was similar for t quenched drug linker.

Total impurities in the solution did not change after long term e at 25º C The reconstituted solution was analyzed to determine the percent of total impurities.

At the initial time point, the percent was not more than 0.007. After reconstitution following storage for one month at 25º C (60% relative humidity), the percent was not more than 0.005.

After reconstitution following storage for three months at 25º C (60% relative humidity), the percent was not more than 0.006. After reconstitution ing storage for six months at 25º C (60% relative humidity), the percent was not more than 0.005. Thus, the percent at all times points was similar for total ties.

Particulate contamination of the solution not affected by long term storage at 25º C Particulate contamination was assessed by determining sible particles. ance criteria was met by determining the number of particles greater than 10 µm per container, with no more than 6000 (USP (US Pharmacopeia) and European Pharmacopoeia standard). At the initial time point, the number of particles per container greater than 10 µm was 33. After reconstitution following storage for one month at 25º C (60% relative humidity), the number of particles per container greater than 10 µm was 18. After reconstitution following storage for three months at 25º C (60% relative humidity), the number of particles per container greater than 10 µm was 25. After reconstitution following storage for six months at 25º C (60% relative humidity), the number of particles per container greater than 10 µm was 50. Thus, all time points met with the acceptance ia for the number of particles per container greater than 10 µm. Acceptance criteria was also met by determining the number of particles greater than 25 µm per container, with not more than 600. At the l time point, the number of particles per container greater than 25 µm was 0.

After reconstitution following e for one month at 25º C (60% relative humidity), the number of les per container greater than 25 µm was 2. After reconstitution following storage for three month at 25º C (60% relative humidity), the number of particles per container greater than 25 µm was 2. After reconstitution ing storage for six months at 25º C (60% relative humidity), the number of particles per container greater than 25 µm was 2. Thus, all time points met with the acceptance criteria for the number of particles per container greater than 25 µm.

Water content of the solution not affected by long term storage at 25º C Water content was assessed by Karl-Fischer-Titration. At the initial time point, the percent water in the reconstituted solution was 2.0%. After titution following storage for one month at 25º C (60% relative humidity), the percent water in the reconstituted solution was undetectable. After reconstitution following storage for three months at 25º C (60% relative humidity), the t water in the tituted solution was 0.8%. After titution following storage for six months at 25º C (60% relative humidity), the percent water in the tituted solution was 0.9%. Thus, at the initial time point, and after reconstitution following storage for one, three and six months, the water content of the reconstituted solution was negligible. pH of the solution not affected by long term storage at 25º C pH of the reconstituted solution was determined at the initial time point, and after reconstitution following storage for three and six months at 25º C (60% relative humidity).

At the l time point, the pH value of the reconstituted solution was 6.0. After reconstitution following storage for three months at 25º C (60% relative humidity), the pH value of the reconstituted solution was 5.9. After reconstitution following e for six months at 25º C (60% relative humidity), the pH value of the reconstituted solution was 5.9.

Example 5: Stability of the ADC 1-MMAF Lyophilized Formulation at 40 ºC The following tests were performed after reconstitution of the lyophilized ADC1- MMAF formulation describe in Example 2, with SWFI at the initial time point, and after reconstitution following e of the lyophilizate for one, three and six months at 40º C/(75% relative ty): Appearance of lyophilizate and reconstituted solution not impacted by long term storage at 40º C Appearance of the lizate and of the reconstituted solution was visually assessed to confirm lyophilizate was practically free from visible foreign particulate matter and free from moisture in packaging material. At the initial time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity), the appearance of the lyophilizate complied with the foregoing criteria. After reconstitution, the reconstituted solution was a colorless to slightly yellow solution, practically free from visible particulate matter. At the initial time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity), the appearance of the reconstituted solution a colorless to slightly yellow solution, cally free from visible particulate matter.

Color of solution not impacted by long term storage at 40º C Color of solution (visual) was assessed using a BY-scale, where the s were tested against a reference on and the values were ed. At the initial time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity), all reconstituted solutions had a BY-scale measure less than or equal to 7. Thus, storage did not affect the color of the solution.

Clarity and Opalescence of solution not affected by long term storage at 40º C Clarity and cence of the reconstituted solution was assessed. ance ia of the reconstituted solution was met if the reconstituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, Ph. Eur. At the initial time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity), the ance of the tituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, Ph. Eur.) (< = RSII).

Biological activity of solution not affected by long term storage at 40º C A xicity assay using a human epidermoid carcinoma cell line was used to test the biological activity (%) of the reconstituted solution in comparison to an ADC1-MMAF control which had been previously confirmed to have cytotoxic activity (the control having 100% activity). At the initial time point, ical ty was 109%. After reconstitution following storage at 40º C (75% relative humidity) for one month, relative biological activity was 117%. After reconstitution following storage at 40º C (75% relative humidity) for three months, relative biological activity was 113%. After titution following storage at 40º C (75% relative humidity) for six months, relative biological activity was 110%. Thus, the percent biological activity at all times points had biological activity over 100%.

Size of molecules and/or molecular complexes not affected by long term storage at 40º C Size exclusion chromatograph was performed by Size Exclusion-High Performance Liquid Chromatograph (SE-HPLC). The main peak (%) was measured in addition to high molecular weight s (%) and low molecular weight species (%). At the initial time point, the main peak was 98.9%. High molecular weight species were 0.9% and low molecular weight species were 0.2%. After reconstitution following storage for at 40º C (75% relative humidity) one month, the main peak was 98.8%. High molecular weight species were 1.0% and low molecular weight species were 0.2%. After reconstitution following storage at 40º C (75% relative humidity) for three months, the main peak was 98.7%. High molecular weight species were 1.1% and low molecular weight species were 0.2%. After reconstitution following storage at 40º C (75% ve humidity) for six months, the main peak was 98.8%. High molecular weight species were 1.0% and low molecular weight species were 0.2%. Thus, there was little to no change in main peak % and high and low molecular weight species among l, one, three and six month ements.

Chromatographic peak of the solution ged by long term storage at 40º C Cation exchange chromatography (CEX) was performed by High Performance Liquid Chromatography (CEX-HPLC). At the initial time point, and after reconstitution following e at 40º C (75% relative humidity) for one month, three months and six months the ance of the reconstituted solution was characterized by a predominant chromatographic peak pattern of the sample conforms to that of the nce standard.

Purity of the solution not affected by long term storage Capillary gel electrophoresis (CE-SDS-R) was performed on the reconstituted solution at the initial time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity) and was used to determine the percent purity of the on. At the initial time point, the percent purity was 97.4%. After reconstitution following storage for one month, the percent purity was 97.5%. After reconstitution ing storage for three , the percent purity was 96.9%. After reconstitution following storage for six months, the percent purity was 97.2%. Thus, the purity of the tituted solution did not significantly change between the initial time point, and at and after reconstitution following storage for one, three and six months at 40º C (75% ve humidity).

Drug to antibody ratio of the solution unchanged after long term storage at 40º C Hydrophobic interaction chromatography (HIC) was performed on the reconstituted solution. At the l time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity), DAR was measured as 4.2 for all reconstituted solutions.

Percent unconjugated antibody in the solution unchanged after long term storage at 40º C At the initial time point, the percent was not more than 4.1. After reconstitution following storage for one month at 40º C (75% relative humidity), the percent was not more than 4.1. After reconstitution following storage for three months at 40º C (75% relative humidity), the percent was not more than 4.1. After reconstitution following storage for six months at 40º C (75% relative humidity), the percent was not more than 3.9. Thus, the percent at all times points was similar.

Percent quenched drug linker in the solution not changed by long term e at 40º C Reversed phase chromatography (RP-HPLC) was med on the tituted solution to determine the percent quenched drug linker. At the initial time point, the percent was not more than 0.007. After reconstitution following storage for one month at 40º C (75% relative humidity), the percent was not more than 0.005. After reconstitution following storage for three months at 40º C (75% relative humidity), the percent was not more than 0.006. After reconstitution ing storage for six months at 40º C (75% relative humidity), the percent was not more than 0.005. Thus, the percent at all times points was similar for percent quenched drug linker.

Total impurities in the solution did not change after long term storage at 40º C The reconstituted solution was analyzed to determine the percent of total impurities using RP-HPLC. At the initial time point, the percent was not more than 0.007. After reconstitution following storage for one month at 40º C (75% relative humidity), the percent was not more than 0.005. After reconstitution ing storage for three months at 40º C (75% relative ty), the percent was not more than 0.006. After reconstitution following storage for six months at 40º C (75% relative ty), the percent was not more than 0.005.

Thus, the percent at all times points was similar for total impurities.

Particulate contamination of the on not ed by long term storage at 40º C Particulate contamination was assessed by determining sub-visible particles.

Acceptance criteria was met by determining the number of particles r than 10 µm per container, with not more than 6000 (USP (US Pharmacopeia) and European Pharmacopoeia standard). At the initial time point, the number of particles per container greater than 10 µm was 33. After titution following e for one month at 40º C (75% relative humidity), the number of particles per container greater than 10 µm was 5. After reconstitution following storage for three months at 40º C (75% relative humidity), the number of particles per container greater than 10 µm was 12. After reconstitution following storage for six months at 40º C (75% relative humidity), the number of particles per container greater than 10 µm was 32. Thus, all time points met with the acceptance criteria for the number of particles per container greater than 10 µm. Acceptance criteria was also met by determining the number of particles r than 25 µm per container, with not more than 600. At the initial time point, the number of particles per container r than 25 µm was 0.

After reconstitution following storage for one month at 40º C (75% relative humidity), the number of particles per container greater than 25 µm was 0. After reconstitution following storage for three month at 40º C (75% ve humidity), the number of particles per container greater than 25 µm was 0. After reconstitution following storage for six months at 40º C (75% relative humidity), the number of particles per container greater than 25 µm was 2. Thus, all time points met with the acceptance criteria for the number of les per container greater than 25 µm.

Water content of the solution not affected by long term storage at 40º C Water content was assessed by Karl-Fischer-Titration. Karl Fischer titration uses coulometric or volumetric titration to determine trace amounts of water in a sample, reported as a t. At the l time point, the percent water in the reconstituted solution was 2.0%. After reconstitution following storage for one month at 40º C (75% ve humidity), the percent water in the reconstituted solution was undetectable. After reconstitution following storage for three months at 40º C (75% relative humidity), the percent water in the reconstituted solution was 0.9%. After reconstitution following e for six months at 40º C (75% relative humidity), the percent water in the tituted solution was 1.0%. Thus, at the initial time point, and after reconstitution following e for one, three and six months, the water content of the reconstituted solution was negligible. pH of the on not affected by long term storage at 40º C pH of the reconstituted solution was determined at the initial time point, and after reconstitution following storage for one, three and six months at 40º C (75% relative humidity). At the initial time point, the pH value of the tituted solution was 6.0. After reconstitution following storage for three months at 40º C (75% relative humidity), the pH value of the reconstituted solution was 5.9. After reconstitution following storage for six months at 40º C (75% relative humidity), the pH value of the tituted solution was 5.9.

Purification of ADC 1-MMAF was performed in accordance with the batch purification method described herein, and disclosed in U.S. Provisional Application No. 834 and U.S. Application No. 14/210,602, filed on March 14, 2014, the contents of which are incorporated by reference herein. The average DAR for ADC mixtures comprising ADC1-MMAFp described in Examples 6 to 8 was about 3.0.

Stability experiments described in Examples 6 to 8 were performed after reconstitution with SWFI at an initial time point, and after reconstitution following storage of the lyophilizate comprising ADC1-MMAFp for three months at 5º C, and for one and three months at both 25º C (60% relative humidity) and 40º C/(75% ve humidity).

Example 6: Stability of Purified ADC 1-MMAF (ADC1-MMAFp) in a Lyophilized Formulation at 5º C The following tests were performed after reconstitution of the lyophilized ADC1- MMAFp formulation described in Example 2, with SWFI at the l time point, and after reconstitution of the formulation following storage of the lyophilizate for up to three months at 5º C.

Appearance of lyophilizate and reconstituted solution not impacted by long term storage at 5º ance of the lyophilizate and of the reconstituted solution was ly assessed to confirm that the lyophilizate was practically free from visible foreign particulate matter and free from moisture in packaging material. At the initial time point, and after reconstitution following storage at 5º C for three months, the ance of the lyophilizate complied with the foregoing criteria. After reconstitution, the reconstituted solution was a colorless to slightly yellow solution, and was practically free from visible particulate matter.

Color of on not impacted by long term storage at 5º C Color of the reconstituted solution (visual) was assessed using a Blue / Yellow scale (BY-scale), where the samples were tested against a nce solution and the values reported. At the initial time point, and after reconstitution following storage at 5º C for three months, all reconstituted solutions had a BY-scale e less than or equal to 7. Thus, storage of the ADC1-MMAFp formulation did not affect the color of the solution.

Clarity and opalescence of solution not ed by long term storage at 5º C Clarity and opalescence of the reconstituted solution was assessed. At the initial time point, and after reconstitution following storage at 5º C for three months, the appearance of the reconstituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, ph. Eur) (< = RSII). ical activity of solution not ed by long term storage at 5º C A cytotoxicity assay using a human epidermoid carcinoma cell line was used to test the biological activity (%) of the reconstituted solution in comparison to an ADC1-MMAF control which had been previously confirmed to have cytotoxic activity (the control having 100% activity). At the initial time point, relative biological activity was 102%. After reconstitution following storage at 5º C in a lyophilized form for three months, relative biological activity was 98%.

Size of molecules and/or molecular complexes not affected by long term storage at 5º C Size exclusion chromatography of the reconstituted solution was performed using Size Exclusion-High Performance Liquid Chromatography (SE-HPLC). The main peak (%) was ed in addition to high molecular weight species (%) and low molecular weight species (%). At the initial time point, the main peak was 99.5%. High molecular weight species were 0.2% and low molecular weight species were 0.2%. After reconstitution following storage at 5º C in a lyophilized form for three months, the main peak was 99.6%.

High molecular weight species were 0.2% and low molecular weight species were 0.2% at both initially and when tituted following three months of storage in lized form.

Thus, all time points showed little to no change in the main peak % and high and low molecular weight species among the initial and three month time point measurements.

Chromatographic peak of the solution unchanged by long term storage at 5º C Cation exchange chromatography (CEX) was performed on the reconstituted on using High Performance Liquid Chromatography (CEX-HPLC). In cation exchange tography, positively d molecules are attracted to a negatively charged solid support. At the initial time point, and after titution following storage at 5º C in lyophilized form for three months the appearance of the tituted solution was characterized by a inant tographic peak pattern of the sample that conformed to that of a l which was the ADC1-MMAF which had been previously characterized.

Thus, the chromatographic peak remained relatively unchanged over the course of three months at 5º C.

Purity of the solution not affected by long term storage at 5º C Capillary gel electrophoresis (CE-SDS-R) was med on the reconstituted solution at the initial time point, and after reconstitution following e at 5º C for three months to determine the purity of the solution. At the initial time point, the percent purity was 97.4%. After reconstitution following e at 5º C in lized form for three months, the percent purity was 97.6%. Thus, the purity of the reconstituted on did not significantly change between the initial time point and three months of storage.

Drug to antibody ratio (DAR) of ADC1-MMAF ed unchanged after storage at 5º C Hydrophobic interaction chromatography (HIC) was performed on the reconstituted solution in order to determine the drug to antibody ratio (DAR) over a three month storage period. HIC is used to separate proteins on the basis of relative hydrophobicity. At the initial time point, and after titution following storage in lyophilized form at 5º C for three months, the average drug to antibody ratio (DAR) for ADC1-MMAF was measured as 3.0 and 2.9, respectively.

Percent unconjugated antibody 1 in the solution unchanged after storage at 5º C The reconstituted solution was also analyzed to determine the percent unconjugated antibody for MAF. At the initial time point, the percent was not more than 7.6.

After reconstitution ing storage at 5º C in lyophilized form for three months, the percent was not more than 7.6. Thus, the percent of unconjugated antibody 1 remained the same over the three month period.

Percent quenched drug linker in the solution unchanged by storage at 5º C Reversed phase chromatography LC) was performed on the reconstituted solution to determine the percent quenched drug linker. The percent of quenched drug linker was not detected both initially and after reconstitution following storage at 5º C for three months in lyophilized form (the practical limit of detection was 0.001%).

Total impurities in the solution unchanged after storage at 5º C Reconstituted solution was also analyzed to determine the percent of total impurities using RP-HPLC. The percent of total impurities was not detectable both initially and after reconstitution following storage at 5º C for three months in lyophilized form (the cal limit of detection was 0.001%; practical limit of quantitation was 0.003%).

Particulate contamination of the solution not affected by storage at 5º C Particulate contamination was assessed by determining sub-visible particles using two different acceptance ia. ance criteria was met by determining the number of particles greater than 10 µm per ner, with not more than 6000 (USP (US Pharmacopeia) and European copoeia standard). At the initial time point, the number of particles per ner greater than 10 µm was 13. After reconstitution following storage at 5º C for three months in lized form, the number of particles per container greater than 10 µm was 20. Thus, both time points met with the acceptance ia for the number of particles per container greater than 10 µm.

Acceptance criteria was also met by determining the number of particles greater than µm per container, with NMT of 600 (USP (US Pharmacopeia) and European Pharmacopoeia standard). At the initial time point, the number of particles per container r than 25 µm was 0. After reconstitution following e at 5º C for three months, the number of particles per container greater than 25 µm was 0. Thus, both time points met with the acceptance criteria for the number of particles per container greater than 25 µm.

Water content of the solution not affected by storage at 5º C Water content was assessed by Karl-Fischer-Titration. Karl Fischer titration uses coulometric or volumetric titration to determine trace amounts of water in a , reported as a percent. At the initial time point, the percent water in the reconstituted solution was 0.8%. After reconstitution following e at 5º C for three months in lyophilized form, the percent water in the reconstituted solution was 0.8%. Thus, at the initial time point and after titution following storage at 5º C for three months, the water content of the reconstituted solution was ible. pH of the solution not affected by storage at 5º C pH of the reconstituted solution was determined at the initial time point, and after reconstitution following storage at 5º C for three months. At the initial time point, the pH value of the reconstituted solution was 5.9. After storage at 5º C for three months, the pH value of the reconstituted solution was 5.9. Thus, storage of the ADC1-MMAFp composition for three months at 5º C did not affect pH.

Example 7: Stability of ADC 1-MMAFp in a lized Formulation at 25º C The following experiments were performed after reconstitution of the lyophilized ADC1-MMAFp formulation (see Example 2) with SWFI at the initial time point, and after titution following storage of the lyophilizate for one and three months at 25º C (60% ve humidity).

Appearance of lyophilizate and reconstituted solution not ed by storage at 25º C Appearance of the lyophilizate and of the reconstituted solution was visually ed to confirm lizate was practically free from visible foreign particulate matter and free from moisture in packaging material. At the initial time point, and after reconstitution following storage for one and three months at 25º C, the appearance of the lizate complied with the foregoing criteria. After reconstitution, the reconstituted solution was a colorless to slightly yellow on, practically free from visible particulate matter. Thus, at the initial time point, and after reconstitution following storage for one and three months at 25º C, the appearance of the reconstituted solution was that the on was colorless to slightly yellow solution, and practically free from visible particulate matter.

Color of solution not impacted by storage at 25º C Color of solution (visual) was assessed using a Blue/Yellow (BY)-scale where the samples were tested against a reference solution and the values were ed. At the initial time point, and after reconstitution following storage for one and three months at 25º C, all reconstituted solutions had a BY-scale measure less than or equal to 7. Thus, storage did not affect the color of the solution.

Clarity and opalescence of on not affected by storage at 25º C Clarity and opalescence of the reconstituted solution was assessed. ance criteria of the reconstituted solution was met if the reconstituted solution was not more opalescent than reference suspension IV (per European copeia, ph. Eur.).At the initial time point, and after reconstitution following storage for one and three months at 25º C, the ance of the reconstituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, ph. Eur.) (< = RSII).

Biological activity of solution not affected by storage at 25º C A cytotoxicity assay using a human epidermoid carcinoma cell line was used to test the biological activity (%) of the reconstituted solution in comparison to an ADC1-MMAF control which had been previously confirmed to have cytotoxic activity (the control having 100% activity. At the initial time point, relative biological activity was 102%. After reconstitution following storage at 25º C for one month, relative biological ty was 101%. After reconstitution following storage at 25º C for three months, relative biological activity was 97%.

Size of molecules and/ or molecular complexes not ed by e at 25º C Size ion chromatograph was performed by Size Exclusion-High Performance Liquid Chromatography (SE-HPLC). The main peak (%) was ed, in on to high molecular weight s (%) and low molecular weight species (%). At the initial time point, the main peak was 99.5%. High molecular weight species were 0.2% and low molecular weight s were 0.2%. After reconstitution following storage for at 25º C one month, the main peak was 99.5%. High molecular weight species were 0.3% and low molecular weight species were 0.2%. After reconstitution following storage at 25º C for three months, the main peak was 99.6%. High molecular weight species were 0.3% and low molecular weight species were 0.2%. Thus, there was little to no change in main peak % and high and low molecular weight species among initial, one and three month measurements.

Chromatographic peak of the solution unchanged by storage at 25º C Cation exchange chromatography (CEX) was performed by High mance Liquid Chromatography (CEX-HPLC). At the initial time point, and after reconstitution ing storage at 25º C for one month and three months the appearance of the reconstituted solution was characterized by a inant chromatographic peak n of the sample that conformed to that of a nce standard.

Purity of the solution not affected by e at 25º C Capillary gel electrophoresis (CE-SDS-R) was performed on the reconstituted solution at the initial time point, and after reconstitution following storage for one and three at 25º C. At the initial time point, the percent purity was 97.4%. After reconstitution following storage for one month, the percent purity was 97.5%. After reconstitution following storage for three months, the percent purity was 97.6%. Thus, the purity of the reconstituted solution did not significantly change between the initial time point, and after reconstitution following storage for one and three months at 25º C.

Drug to antibody ratio (DAR) of ADC1-MMAFp in the solution remained unchanged after storage at 25º C Hydrophobic interaction chromatography (HIC) was performed on the reconstituted solution. At the initial time point, DAR was measured as 3.0. After titution following storage for one month at 25º C, DAR was measured as 3.0. After reconstitution following storage for three months at 25º C, DAR was measured as 2.9. Thus, DAR of ADC1-MMAFp did not significantly change between the initial time point, and after reconstitution following storage for one and three months at 25º C.

Percent unconjugated antibody 1 in the solution unchanged after storage at 25º C The reconstituted solution was analyzed to determine the percent unconjugated antibody 1. At the initial time point, the percent was not more than 7.6. After reconstitution following storage for one month at 25º C, the percent was not more than 7.6. After titution ing storage for three months at 25º C, the percent was not more than 7.6.

Percent ed drug linker in the on not changed by storage at 25º C Reversed phase chromatography (RP-HPLC) was performed on the reconstituted solution to determine the percent quenched linker. At the initial time point, the one month time point, and the three month time point, the percent of quenched linked was not detectable (practical limit of detection was 0.001%; practical limit of quantitation was 0.003%).

Total ties in the solution did not change after storage at 25º C The reconstituted solution was ed to determine the percent of total impurities.

At the initial time point, the percent was not detected. After reconstitution ing storage for one month at 25º C, the percent of impurities was less than 0.003. After reconstitution following storage for three months at 25º C, the percent was not detected (practical limit of detection was 0.001%; cal limit of quantitation was 0.003%). Thus, the percent at all times points was similar for total impurities.

Particulate contamination of the solution not affected by storage at 25º C Particulate contamination was ed by determining sub-visible particles according to two acceptance criteria. ance criteria was met by determining the number of particles greater than 10 µm per container, with no more than 6000 (USP (US Pharmacopeia) and European Pharmacopoeia standard). At the initial time point, the number of particles per container greater than 10 µm was 13. After titution following e for one month at 25º C, the number of particles per container greater than 10 µm was 12. After reconstitution following storage for three months at 25º C, the number of les per container r than 10 µm was 17. Thus, all time points met with the acceptance criteria for the number of particles per container greater than 10 µm. Acceptance criteria was also met by determining the number of particles greater than 25 µm per container, with not more than 600. At the initial time point, the number of les per container greater than 25 µm was 0. After reconstitution following storage for one month at 25º C, the number of particles per container greater than 25 µm was 0. After reconstitution following storage for three month at 25º C, the number of particles per container greater than 25 µm was 7. Thus, all time points met with the acceptance criteria for the number of les per container greater than 25 µm.

Water content of the solution not affected by storage at 25º C Water content was assessed by Karl-Fischer-Titration. At the initial time point, the percent water in the reconstituted solution was 0.8%. After reconstitution following e for one month at 25º C, the percent water in the reconstituted solution was 0.8%. After titution following storage for three months at 25º C, the percent water in the reconstituted solution was 0.8%. Thus, at the initial time point, and after reconstitution following storage for one and three months, the water content of the reconstituted solution was negligible. pH of the solution not affected by storage at 25º C pH of the reconstituted solution was determined at the initial time point, and after titution following storage for one and three months at 25º C. At the initial time point, the pH value of the reconstituted solution was 5.9. After reconstitution following storage for three months at 25º C, the pH value of the reconstituted solution was 5.9. After reconstitution following storage for six months at 25º C, the pH value of the reconstituted on was 5.9.

Example 8: ity of ADC 1-MMAFp Lyophilized Formulation at 40 ºC The following tests were performed after reconstitution of the lyophilized ADC1- MMAFp formulation describe in Example 2, with SWFI at the l time point, and after titution following storage of the lyophilizate for one and three months at 40º C/(75% relative humidity).

Appearance of lyophilizate and reconstituted solution not ed by storage at 40º C Appearance of the lyophilizate and of the reconstituted solution was ly assessed to confirm lyophilizate was practically free from visible foreign particulate matter and free from moisture in packaging material. At the initial time point, and after titution following storage for one and three months at 40º C, the appearance of the lyophilizate complied with the foregoing criteria. After reconstitution, the reconstituted solution was a ess to slightly yellow solution, practically free from visible particulate matter. At the initial time point, and after reconstitution following storage for one and three months at 40º C, the appearance of the tituted solution was that the solution was a colorless to ly yellow solution, practically free from visible particulate matter.

Color of solution not impacted by storage at 40º C Color of solution (visual) was assessed using a BY-scale, where the samples were tested against a reference solution and the values were reported. At the initial time point, and after reconstitution following storage for one and three months at 40º C, all reconstituted solutions had a BY-scale measure less than or equal to 7. Thus, storage did not affect the color of the solution.

Clarity and Opalescence of solution not affected by storage at 40º C Clarity and opalescence of the reconstituted solution was assessed. Acceptance criteria of the tituted solution was met if the reconstituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, Ph. Eur. At the initial time point, and after reconstitution following storage for one and three months at 40º C, the appearance of the reconstituted solution was not more opalescent than reference suspension IV (per European Pharmacopeia, Ph. Eur.) (< = RSII).

Biological activity of solution not affected by e at 40º C A cytotoxicity assay using a human epidermoid carcinoma cell line was used to test the biological activity (%) of the tituted solution in comparison to an ADC1-MMAF l which had been previously confirmed to have cytotoxic activity (the control having 100% activity). At the initial time point, biological ty was 102%. After titution following storage at 40º C for one month, relative biological ty was 101%. After reconstitution following storage at 40º C for three months, relative biological activity was 105%. Thus, the percent biological activity at all times points had biological activity over 100% in the formulation of Example 2.

Size of molecules and molecular complexes not affected by storage at 40º C Size exclusion chromatograph was performed by Size Exclusion-High Performance Liquid Chromatograph (SE-HPLC). The main peak (%) was measured in addition to high molecular weight species (%) and low molecular weight species (%). At the l time point, the main peak was 99.5%. High molecular weight species were 0.2% and low molecular weight species were 0.2%. After reconstitution following storage for at 40º C one month, the main peak was 99.5%. High molecular weight species were 0.3% and low molecular weight s were 0.2%. After titution following e at 40º C for three months, the main peak was 99.5%. High lar weight species were 0.3% and low molecular weight species were 0.2%. Thus, there was little to no change in main peak % and high and low molecular weight species among initial, one and three month measurements.

Chromatographic peak of the solution unchanged by storage at 40º C Cation exchange chromatography (CEX) was performed by High Performance Liquid Chromatography (CEX-HPLC). At the initial time point, and after reconstitution following storage at 40º C for one month and three months the appearance of the reconstituted solution was characterized by a predominant chromatographic peak pattern of the sample conforms to that of the reference standard.

Purity of the solution not ed by storage at 40º C Capillary gel electrophoresis (CE-SDS-R) was performed on the reconstituted solution at the initial time point, and after reconstitution following e for one, three and six months at 40º C and was used to ine the percent purity of the solution. At the l time point, the percent purity was 97.4%. After reconstitution following storage for one month, the percent purity was 97.5%. After reconstitution following storage for three months, the percent purity was 97.6%. Thus, the purity of the reconstituted solution did not icantly change between the initial time point, and at and after reconstitution following storage for one and three months at 40º C.

Drug to antibody ratio (DAR) of ADC1-MMAFp unchanged after storage at 40º C Hydrophobic ction chromatography (HIC) was performed on the reconstituted solution. At the initial time point, DAR was measured as 3.0. After reconstitution following storage for one month at 40º C, DAR was measured as 3.0. After reconstitution following storage for three months at 40º C, DAR was measured as 2.9. Thus, DAR did not significantly change n the initial time point, and after reconstitution following storage for one and three months at 40º C.

Percent ugated dy 1 in the solution unchanged after storage at 40º C At the initial time point, the percent of unconjugated antibody 1 was not more than 7.6. After reconstitution following storage for one month at 40º C, the percent of unconjugated antibody 1 was not more than 7.6. After reconstitution following storage for three months at 40º C, the percent of unconjugated antibody 1 was not more than 7.6. Thus, the t at all times points was similar.

Percent quenched drug linker in the solution not d by storage at 40º C Reversed phase chromatography (RP-HPLC) was performed on the reconstituted solution to determine the percent quenched drug linker. At the initial time point, the percent was not detected. After reconstitution following storage for one month at 40º C, the percent was not detected. After reconstitution following storage for three months at 40º C, the t was not detected. Thus, the percent quenched drug linker at all times points was not detected.

Total impurities in the solution did not change after storage at 40º C The reconstituted solution was analyzed to determine the percent of total ties using RP-HPLC. At the l time point, the percent was not detected. After reconstitution following storage for one month at 40º C, the percent was less than 0.003. After reconstitution following storage for three months at 40º C, the percent was not detected.

Thus, the percent at all times points was r for total impurities.

Particulate contamination of the solution not affected by storage at 40º C Particulate contamination was assessed by determining sub-visible particles according to two acceptance criteria. ance ia was met by determining the number of particles greater than 10 µm per container, with not more than 6000 (USP (US Pharmacopeia) and European Pharmacopoeia standard). At the initial time point, the number of particles per container greater than 10 µm was 13. After reconstitution following storage for one month at 40º C, the number of particles per container greater than 10 µm was 5. After reconstitution following storage for three months at 40º C, the number of particles per ner greater than 10 µm was 8. Thus, all time points met with the acceptance criteria for the number of les per container greater than 10 µm.

Acceptance criteria was also met by determining the number of particles greater than µm per container, with not more than 600. At the initial time point, the number of les per ner greater than 25 µm was 0. After reconstitution following storage for one month at 40º C, the number of particles per container greater than 25 µm was 0. After reconstitution following storage for three month at 40º C, the number of particles per container greater than 25 µm was 2. Thus, all time points met with the acceptance ia for the number of les per container greater than 25 µm.

Water content of the solution not affected by storage at 40º C Water content was assessed by Karl-Fischer-Titration. Karl Fischer ion uses coulometric or volumetric titration to determine trace amounts of water in a sample, reported as a percent. At the initial time point, the percent water in the reconstituted solution was 0.8%. After reconstitution following storage for one month at 40º C, the percent water in the reconstituted solution was 0.8%. After reconstitution following storage for three months at 40º C, the percent water in the reconstituted solution was 0.8%. Thus, at the initial time point, and after reconstitution following storage for one and three months, the water content of the reconstituted on was negligible. pH of the solution not affected by storage at 40º C pH of the reconstituted on was determined at the initial time point, and after reconstitution following storage for one and three months at 40º C. At the initial time point, the pH value of the reconstituted solution was 5.9. After reconstitution following storage for three months at 40º C, the pH value of the reconstituted solution was 5.9. After reconstitution following storage for six months at 40º C, the pH value of the reconstituted solution was 5.9.

Example 9: Large Scale Manufacturing of Lyophilized ADC 1-MMAF Formulation For the preparation of the bulk solution, histidine was dissolved in water for injection, pH was adjusted with hydrochloric acid 10% w/w, and water for injection was added to the final . The formulation buffer excipients (sucrose and polysorbate 80) were weighed and dissolved in 15 mM histidine solution. The resulting solution was then examined for appearance.

ADC 1-MMAF was thawed at 30°C in a water bath, examined for appearance, pooled and weighed. 15 mM histidine buffer, polysorbate 80, and sucrose were added to ADC 1- MMAF. The appearance of the solution was ed and its pH and density determined, followed by sterile filtration. The solution was then lized under controlled conditions.

The critical in-process tests that were carried out during the manufacture of ADC 1- MMAF Powder for Injection Solution, 20 mg/mL are listed in Table 2, below.

Table 2. In-Process Control Tests and Acceptance Limits Operation Test ance Limit First filtration Filter Integrity d flow test, diffusion rate or bubble point must comply with the filter specification Sterilization by filtration Bioburden prior to second < 10 CFU/100 mL Filter Integrity Forward flow test, ion rate or bubble point must comply with the filter specification The amount of ADC 1-MMAF and buffer solution used for a typical batch of ADC 1- MMAF solution for lyophilization are shown in Table 3, below. A list of components and the s used to manufacture the formulation buffer are described in Table 4 and Table 5.

Table 3. Batch Formula for ADC 1-MMAF Bulk Drug Product Solution Dosage Strength 20 mg/mL Batch Size 27 L a Component Amount (kg) per Batch ADC 1-MMAF Drug Substance 15.57 b, c, d Formulation Buffer e 12.29 d a. y of bulk solution: 1.032 g/mL b. Equivalent to 0.540 kg of protein at 35 g protein/L drug substance concentrate; y of drug substance concentrate: 1.0089 g/mL c. Drug nce concentrate contains 15 mM histidine d. Amounts vary depending on actual protein concentration of drug substance concentrate e. The batch formula for this material is presented in Table 4 Table 4. Batch Formula for Formulation Buffer Solution Batch Size 11.58 L a Component b Amount (g) per Batch Sucrose 1890 b Polysorbate 80 2.7 c mM Histidine Solution d ad 12290 Abbreviation: ad = to total weight of a. Density of solution: 1.0616 g/mL b. Amount ponds to a final concentration in the bulk product solution of 70 g/L c. Amount corresponds to a final concentration in the bulk product solution of 0.10 g/L d. The batch a for this material is presented in Table 6 .

Table 5. Batch Formula for 15 mM Histidine Solution Batch Size 15 L a Component Amount (g) per Batch Histidine 34.95 hloric Acid 10% (w/w) b q.s Water for Injection ad 14999 Abbreviation: ad = to total weight of a. Density of solution: 0.9993 g/mL b. Used for pH adjustment It is understood that the examples and embodiments described herein are for illustrative purposes only and that various cations or changes in light thereof will be ted to persons skilled in the art and are to be included within the spirit and purview of the appended claims. All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety for all purposes.

Y OF SEQUENCES SEQ ID NO: 1 Nucleic acid Variable heavy chain sequence of antibody 2 e anti-EGFR SEQ ID NO: 2 Protein Variable heavy chain sequence of antibody 2 (murine anti-EGFR SEQ ID NO: 3 c acid le light chain sequence of antibody 2 (murine anti-EGFR SEQ ID NO: 4 Protein Variable light chain sequence of dy 2 (murine anti-EGFR SEQ ID NO: 5 n CDR1 of the variable heavy chain sequence SEQ ID NO:2 SEQ ID NO: 6 Protein CDR2 of the variable heavy chain sequence SEQ ID NO:2 SEQ ID NO: 7 n CDR3 of the variable heavy chain sequence SEQ ID NO:2 SEQ ID NO: 8 Protein CDR1 of the variable light chain sequence SEQ ID NO:2 SEQ ID NO: 9 Protein CDR2 of the variable light chain sequence SEQ ID NO:2 SEQ ID NO: 10 Protein CDR3 of the variable light chain sequence SEQ ID NO:2 SEQ ID NO: 11 Protein le heavy chain sequence of antibody 2 (murine anti-EGFR Ab) without signal peptide SEQ ID NO: 12 Protein Variable light chain sequence of antibody 2 (murine anti-EGFR Ab) without signal peptide SEQ ID NO: 13 Protein Variable heavy chain sequence of antibody 1 (humanized anti- EGFR Ab) SEQ ID NO: 14 Protein Constant heavy chain ce of antibody 1 (humanized anti- EGFR Ab) SEQ ID NO: 15 Protein CDR1 of the variable heavy chain sequence SEQ ID NO:13 SEQ ID NO: 16 Protein CDR2 of the variable heavy chain sequence SEQ ID NO:13 SEQ ID NO: 17 Protein CDR3 of the variable heavy chain sequence SEQ ID NO:13 SEQ ID NO: 18 Protein Variable light chain sequence of antibody 1 (humanized anti- EGFR Ab) SEQ ID NO: 19 Protein Constant light chain sequence of antibody 1 (humanized anti- EGFR Ab) SEQ ID NO: 20 Protein CDR1 of the variable light chain sequence SEQ ID NO:18 SEQ ID NO: 21 Protein CDR2 of the variable light chain sequence SEQ ID NO:18 SEQ ID NO: 22 n CDR3 of the variable light chain sequence SEQ ID NO:18 We

Claims (27)

claim:

1. A lyophilized formulation comprising an anti-Epidermal Growth Factor Receptor (EGFR) dy drug conjugate (ADC), a sugar, a buffer, and a surfactant, n said ation has a pH of about 5 – 7 upon reconstitution, wherein said anti-EGFR ADC comprises an anti-EGFR antibody conjugated to an auristatin, wherein the antibody is an IgG antibody comprising a heavy chain variable region comprising mentarity domain regions (CDRs) comprising the amino acid ces set forth in SEQ ID NOS: 15, 16, and 17, and comprising a light chain variable region comprising CDRs comprising the amino acid sequences set forth in SEQ ID NOS: 20, 21, and 22 and wherein the buffer is selected from the group consisting of acetate, succinate, gluconate, methionine, imidazole, histidine, glycine, arginine, citrate, phosphate, and citrate and phosphate.

2. The formulation of claim 1, wherein the auristatin is Monomethylauristatin F (MMAF).

3. The ation of claim 2, wherein the MMAF is ated to the antibody with a maleimidocaproyl linker.

4. The formulation of any one of claims 1-3, wherein the surfactant is a polysorbate or a poloxamer.

5. The formulation of claim 4, wherein the formulation comprises 0.1-0.9 mg of the polysorbate.

6. The formulation of claim 4 or 5, wherein the polysorbate is polysorbate 80.

7. The formulation of any one of claims 1-6, wherein the formulation ses about 1- 150 mg of the anti-EGFR ADC.

8. The formulation of any one of claims 1-7, wherein the formulation comprises about 320- 410 mg of the sugar.

9. The formulation of any one of claims 1-8, wherein the sugar is selected from the group consisting of ol, sorbitol, sucrose, and trehalose.

10. The formulation of any one of claims 1-9, comprising about 1-20 mg of the .

11. The formulation of any one of claims 1-10, wherein the formulation has a pH of about 5.5 to 6.5 upon reconstitution.

12. The formulation of any one of claims 1-11, wherein the dy comprises a heavy chain le region comprising the amino acid sequence set forth in SEQ ID NO: 13, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 18.

13. The formulation of any one of claims 1-11, wherein the antibody comprises a heavy chain constant region comprising the amino acid sequence as set forth in SEQ ID NO: 14.

14. The formulation of any one of claims 1-12, wherein the antibody comprises light chain constant region comprising the amino acid sequence as set forth in SEQ ID NO: 19.

15. The formulation of claim 1, comprising 0.1-0.9 mg of polysorbate 80.

16. The formulation of claim 1, comprising 320-410 mg of sucrose.

17. The formulation of claim 1, comprising 1-150 mg of the anti-EGFR ADC, 1-20 mg of histidine, 0.1-0.9 mg of polysorbate 80, and 320-410 mg of sucrose.

18. The formulation of claim 17, comprising 90-120 mg of the anti-EGFR ADC.

19. The formulation of claim 1, wherein less than 5% of the anti-EGFR ADC is ed and/or aggregated upon titution as determined by Size Exclusion Chromatography (SEC) analysis.

20. The formulation of claim 1, wherein the pH is about 5.5.

21. The formulation of claim 1, wherein the formulation is packaged in a glass vial.

22. Use of the formulation according to any one of claims 1-21, in the manufacture of a ment for treating cancer.

23. The use according to claim 22, wherein the cancer is selected from the group consisting of: glioblastoma, non-small cell lung cancer, lung cancer, colon cancer, head and neck cancer, breast cancer, squamous cell , anal cancer, skin cancer, and vulvar cancer.

24. The use according to claim 22, wherein the cancer is selected from the group consisting of squamous tumors, glioblastoma, glioma, non-small cell lung cancer (NSCLC), lung cancer, colon , head and neck cancer, breast , anal cancer, skin cancer, and vulvar cancer.

25. The use according to claim 24, wherein the squamous tumor is selected from the group consisting of squamous lung tumor, a squamous tumor of the head or neck, and a squamous cervical tumor.

26. The use according to claim 22, wherein the cancer is a solid tumor having overexpression of EGFR.

27. The use of any one of claims 22-26, wherein the formulation is formulated for intravenous administration. AbbVie Deutschland GmbH & Co. KG AbbVie Inc. By the eys for the Applicant SPRUSON & FERGUSON I H OCH3 O MMAE ------- HOx° " H f OCH3 N I \ -- 1 N 0 � N MMAE FIG. PABA 0 1 ??1�0;;:x° fJ ---- CATHEPSIN B CLEAVAGE SELF IMMOLATIO r- vcMMAE 1. l (ACTIVE DRUG) I t'�) 2 __,A..__ ,,.-__,A V NH H A · \ (NH O �N 0 ;tJNr VALIN E H ;x CITRULLINE __ _,A...___ V MALEIMIDO CAPROYL _.-_ f MAb $/ +- I ' � N H ' O MMAF OCH3 N � I N 0 OCH3 I l PROTEOLYSIS O �() N mcMMAF N � I (ACTIVE DRUG) c y s-mcMMAF �. .... xI I x,.,., 0 I I o I _ \ 0 \I Y) .A,__ IDO CAPROYL 0 ��:Y O ��..-y o y s 5 S ¢(: Ab :� � 0 +- 140000 • ANTIBODY 1 120000 • ADC1-MMAF • ADC1-MMAE 100000 .____.. ONSET 80000 FLUORESCENCE 60000 .c:� ........,,...- + ••,,,- 40000 20000 0------..-------.---,-------r-----,--�---, 20 30 40 50 60 70 80 90 100 TEMPERATURE 0.00025 ANTIBODY 1 ADC1-MMAE 0.00020 0.00015 Cp 0.00010 (cal/°C) 0.00005 ADC1-MMAF ··. 0.00000 .. -0.00005 - - 20 30 40 50 60 70 80 90 100 TEMPERTAURE0(C) WAVENUMBERS 1695 1675 1655 1635 1615 1595 -0.005 \ a..,. -0.01 �: � -0.015 •a A.U. -0.02 11 II -0.025 41. ll • ANTIBODY1 ·\I·a a• -0.03 • ADC1-MMAF • •• 6AOC1-MMAE • -0.35 ·-· -0.04 WAVELENGTH (nm) 250 260 270 280 290 300 310 0 I • ANTIBODY1 • MAF • ADC1-MMAE NEAR UVCD % • ... ANTIBODY 1 TO AGGREGATES 8 _,.__ ADC1-MMAF TO ADC1-MMAE TO ---- ANTIBODY 1 40C 7d -+-- ADC1-MMAF 40C 7d ·····•···· - 4 ADC1 MMAE40C 7d 2 ........,,...,,.,i ,,,,,,,111,,,,,,,,,, ,,111111••••••1111u1111111u1111111u1111111u1111111u111111.. .,_..·-·-·-·-·---;a,·----------- ------- -·-·-·-·-·-•�•-•..------- 0 ··-- 4 4.5 5 5.5 6 6.5 7 7.5 I ADC1- MMAEHPBCD ADC1- MMAFHPBCD 7d .) OTO - 40C, ADC1-MMAE ADC1-MMAF __ ____ V LOT 2 _ MAE \... HISTIDINE ___ .) V LOT 1 15 mM 5.7 5, d ADC1-MMAF \...____ _ mg/ml, pH 60 7 ANTIBODY 1 9 8 7 6 5 4 3 2 1 ol AGGREGATES 10 +- I (LI z ,....1 ,........,.....,1 0 0 666 g g z zz - ��uo:::FZ _,_ --------- ---------- ----- --=----=coOOIJ