NZ759819B2 - Method of treating or reducing efp - Google Patents

Abstract

Provided is the use of collagenase for the preparation of a medicament for treating or reducing edematous fibrosclerotic panniculopathy (EFP) (cellulite), wherein said medicament is adapted for administration of a plurality of subdermal injections of collagenase comprising collagenase I and collagenase II in a 1:1 mass ratio with a specific activity of 10,000 ABC units per 0.58 mg of collagenase to an area affected by the EFP, wherein the dose of collagenase per injection is between about 5 to about 200 ABC units and the injection sites are about 1 cm to about 4 cm from one another. ase II in a 1:1 mass ratio with a specific activity of 10,000 ABC units per 0.58 mg of collagenase to an area affected by the EFP, wherein the dose of collagenase per injection is between about 5 to about 200 ABC units and the injection sites are about 1 cm to about 4 cm from one another.

Description

METHOD OF TREATING OR REDUCING EFP RELATED APPLICATION This application claims the benefit ofUS. Provisional Application No. 61/549,863 filed October 21, 2011. The entire contents of the above-referenced application are incorporated by reference herein.

BACKGROUND OF THE INVENTION Edematous fibrosclerotic panniculopathy (EFP), more ly ed to as cellulite, is a condition that presents as a topographical alteration in the appearance of the skin and affects about 90% of postpubertal women (Rawlings (2006), Int J Cosmetic Sci 2006; 28: 175-90; Khan et al. , JAm Acad Dermatol 2010; 62: 361-70). EFP appears as dimpled skin and gives the skin what is commonly described as an orange-peel appearance. The dermal septae, composed of enase, are believed to play a causative role in the dimpling of the skin.

Collagenase, an enzyme that has the specific ability to digest collagen, has been used to treat a variety of collagen-mediated diseases, including, for example, Dupuytren’s cture, Peyronie’s disease, lipoma and adhesive capsulitis. US. Patent No. 4,645,668 and US. Patent App. Pub. No. 20070224184 also disclose certain uses of collagenase. A major source of collagenase is from the tation of the bacterium, Clostrz'dz'um histolyticum. An injectable ation comprising C. histolytz'cum collagenase I and enase II is sold under the trade name XIAFLEX® and is approved by the US. Food and Drug Administration (FDA) for the treatment of Dupuytren’s contracture.

W0 2013/059619 PCT/U82012/061063 _ 2 _ The present invention is directed to a method for the ent or reduction of EFP comprising one or a plurality of injections of collagenase to an area affected by EFP.

SUMMARY OF THE INVENTION The present invention is based on the discovery that one or more low dose injections of collagenase to an area affected by EFP are effective to reduce or treat such EFP. The amount of collagenase in a single injection may be as low as 5 ABC units, or 0.00029 mg (0.29 ug). The total dose of collagenase administered depends on the size of the ent area, and is thus between about 5 to about 5000 ABC units. The concentration of collagenase is between about 50 to about 2000 ABC units/milliliter (ml). 10,000 ABC units is equivalent to 0.58 mg collagenase.

In one ment, the invention is directed to a method of treating or reducing EFP in a patient comprising administering to said patient one or a plurality of subdermal injections of collagenase to an area affected by EFP, wherein the dose of enase per injection is between about 5 to about 200 ABC units, and wherein the plurality of subdermal injections are administered at a plurality of injection sites. In certain aspects, a plurality of mal ions are stered at a plurality of injection sites. In additional embodiments, the concentration of enase administered is between about 50 to about 2000 ABC units per milliliter. In certain additional embodiments, each injection of collagenase is administered in a volume of about 0.5 ml or less. In a further aspect, the total dose of collagenase administered is n about 5 to about 2000 ABC units.

In another embodiment, the invention is directed to a method of treating or reducing EFP in a t comprising administering to said patient one or a plurality of subdermal injections of collagenase within an area affected by EFP, wherein the total dose of collagenase administered to the affected area is between about 5 to about 5000 ABC units, and wherein the plurality of injections are administered at a plurality of ion sites. In certain aspects, each injection is between about 5 to about 200 ABC units. In some embodiments, the concentration of collagenase administered is between about 50 to about 2000 ABC units per iter and/or each injection of collagenase is administered in a volume of about 0.5 ml or less.

W0 2013/059619 PCT/U82012/061063 _ 3 _ In yet another embodiment, the invention is a method of treating or ng EFP in a patient comprising stering to said t one or a plurality of subdermal injections of collagenase to an area affected by EFP, wherein the dose of collagenase administered per injection to the affected area is n about 5 to about 200 ABC units and wherein the concentration of collagenase administered to the affected area is between about 50 to about 2000 ABC units per milliliter.

In a fiarther aspect, the ion is ed to a method of treating or reducing EFP in a patient comprising administering one or a plurality of subdermal injections of collagenase to an area affected by EFP wherein the concentration of collagenase administered to the affected area is between about 50 to about 2000 ABC units per milliliter and wherein the volume of each injection of collagenase is about 0.5 ml or less.

In some embodiments, the dose of collagenase administered per injection is between about 5 to about 100 ABC units. In additional embodiments, the dose of collagenase administered per injection is n about 5 to about 50 ABC units.

The collagenase can be derived from a bacterial source or can be a recombinant form of collagenase. In some embodiments, the collagenase is purified from Clostridium histolytz'cum. In an additional embodiment, the collagenase comprises enase I and collagenase II. In yet fiarther embodiments, the collagenase is collagenase I and collagenase II purified from Clostridium histolytz'cum and comprises collagenase I and collagenase II.

BRIEF DESCRIPTION OF THE DRAWINGS The foregoing and other objects, features and advantages of the invention will be apparent from the following more particular description of preferred embodiments of the invention, as illustrated in the accompanying drawings in which like reference characters refer to the same parts hout the different views. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the ples of the invention. is a depiction of the injection template where each dot within the octagon ents an injection site. The X within the circle represents the injection site to the "central dimple." The four comers are labeled as upper right (UR), lower right (LR), upper left (UL), and lower left (LL). is a depiction of buttock and posterior upper thigh with template corner markings. A = Midline of the upper posterior thigh and buttock (from center of the popliteal fossa); C = Template corner; E = Template corner.

DETAILED DESCRIPTION OF THE INVENTION A description of preferred embodiments of the ion follows.

As discussed above, the present invention is based on the discovery that low dose injections of collagenase to an area affected by EFP are ive to lyse collagen and thereby reduce or treat such EFP. The amount of collagenase in a single injection may be as low as 5 ABC units, or 9 mg. The total dose of collagenase stered depends on the size of the ent area, and is thus between about 5 to about 5000 ABC units and/or wherein the concentration of collagenase is between about 50 to about 2000 ABC units/milliliter (ml).

The doses and trations of collagenase employed according to the method of the present invention are substantially lower than the doses and concentrations of collagenase currently used and approved by the U.S. FDA for the treatment of Dupuytren’s contracture.

The words "a" or "an" are meant to encompass one or more, unless otherwise ied.

"Treating" or "treatment" of EFP includes the administration of the compositions or agents described herein to improve the appearance of the skin previously affected by EFP and/or to achieve an ed aesthetic outcome. Treatment of EFP can, for example, encompass a visual reduction in the ty of EFP or a visual ion in the severity or number of skin dimples.

The invention encompasses a method of treating or reducing EFP in a patient comprising administering one or a plurality subdermal injections of collagenase to an area affected by EFP, wherein the plurality of injections are injected at a plurality of injections sites within an area affected by EFP, wherein the dose of collagenase stered per injection is about 5 to about 200 ABC units. In additional embodiments, the dose of collagenase per injection is about 5 to about 100 ABC units, or about 5 to about 50 ABC units, or about 10 to about 100 ABC units, or about 10 to about 50 ABC units. In additional embodiments, the total dose of collagenase administered to the affected area is between about 5 to about 5000 ABC units. The invention also encompasses a method sing administering collagenase to the area affected by EFP wherein the concentration of collagenase administered to the affected area is about 50 to about 2000 ABC units/ml. The _ 5 _ invention additionally encompasses a method of ng or reducing EFP in a patient comprising stering a plurality of injections of collagenase to an area affected by EFP, wherein the dose of collagenase per injection is between about 5 to about 200 ABC units.

An area affected by EFP (also referred to herein as the t area" or "treatment area") is typically an area of the skin on the thighs and/or buttocks characterized by one or more s. In some embodiments, the area of EFP treated with the one or plurality of ions of collagenase is an area of the lateral upper aspect of the thigh or an area of the buttocks and does not involve the gluteal fold. The target area to be treated with collagenase can also be an area having a photonumeric EFP severity scale (CSS) score of Z 10 representing moderate to severe EFP severity within the right or left buttock or the right or left thigh (Hexsel et al. (2009). A validated photonumeric EFP severity scale. JEADV2009; 23:523-52; the contents of which are expressly incorporated by reference herein). The CSS is a photonumeric scale that looks at five key morphologic features of EFP: (A) number of depressions, (B) depth of depressions, (C) morphological appearance of skin surface, (D) laxity, flaccidity or sagging of skin, and (E) the classification scale originally described by Niimberger and Muller, JDermatol Surg Oncol 1978; 4(3): 221-29.) (Hexsel et al., 2009).

Each of these features is evaluated on a 4-point scale from a low of 0 to a high of 3. The scale ranges from 0 to 15.

The target area treated with the one or ity of injections of EFP is generally an area of the skin terized by one or more dimples that are visually evident when the patient is standing. The geometric area of the treatment area depends on the size of the area affected by EFP. Thus, for example, if the area affected by EFP includes one , the ric area of the target area can be about 1 cm2 to about 5 cm2. In additional aspects, the area affected by EFP comprises multiple dimples and has a ric area greater than 1 cm2. In one embodiment, the target area has a geometric area between about 1 cm2 to about 200 cm2. As will be understood, because the target area is generally an area of the thigh or buttocks, the area can, for example, be roughly rectangular in shape and have a length of about 1 to about 15 cm, and a width of about 1 to about 10 cm. In an additional example, the target area has a length of about 6 to about 15 cm and a width of about 4 to about 10 cm. The person of skill in the art will also understand that the target area can be roughly circular or any other ric shape depending on the desired area for treatment. The target area can optionally be characterized by at least one skin dimple approximately at the center of the area W0 2013/059619 PCT/U82012/061063 _ 6 _ of EFP treated, wherein the area of EFP is treated with the one or a plurality of injections.

The sites for injection of collagenase can be numbered and spaced within the area affected by EFP such as to allow for even distribution and efficacy of the injected collagenase. The number of collagenase injections will generally depend on the size of the area to be treated.

In some embodiments, the number of injection sites is at least 1 or more. In other aspects, the number of injection sites is at least about 3 or more. In other aspects, the number of injection sites is at least about 5 or more. In yet other aspects, the number of injection sites is at least about 7 or more. In a further aspect, the number of injection sites is at least 10 or more.

In one embodiment, in which the area to be treated is a single dimple area or ise haVing a geometric area of less than about 5 cm2, there is only a single site of injection, and between about 5 and about 200 ABC units of collagenase is injected. ally, the single injection can be injected into the center of the dimple. In embodiments in which the treatment area is larger, there will be multiple sites of injection and between about 5 to about 200 ABC units of collagenase is administered per injection. Optionally, the ity of injections include at least one injection administered to the center of one dimple.

The sites of injection can, for example, be about 1 to about 4 cm from one r. In yet other aspects, the sites of injection can be about 2 to about 3 cm from one another. For example, in n embodiments, the area affected by EFP has a width about 8 cm and a length of about 10 cm in dimensions and the number of collagenase injections administered is 10 and the distance between injection sites is about 2.5 cm. In certain aspects, an injection template (for e, made of a thin clear material) which includes gs showing the ed injection sites is placed over the target area and the one or more injections are made at the sites indicated by the template.

The target area is treated with one or a plurality of concurrent injections of collagenase. As used herein, concurrent injections are injections administered at the same time or sequentially within the same period of time, i.e., during a single treatment session.

As discussed above, the total dose of collagenase stered to the area affected by EFP is between about 5 to about 5000 ABC units of collagenase. The total dose of collagenase administered depends on the size of the treatment area. The total dose of collagenase is the sum of the doses administered using one or a plurality of injections of collagenase. In certain aspects, each injection of collagenase will comprise equal doses of collagenase. For example, when the number of injections is 10, to be distributed over the treatment area, and each _ 7 _ injection is 200 ABC units of collagenase, the total dose of collagenase to be stered to the target area will be 2000 ABC units. By way of further example, when the number of injections is 10 to be buted over the treatment area, and each injection is 5 ABC units of collagenase, the total dose of collagenase to be administered to the target area will be 50 ABC units. By way of further example, when the number of injections is 5 to be distributed over the treatment area, and, each injection is 5 ABC units of collagenase, the total dose of collagenase to be administered to the target area will be 25 ABC units. When only a single injection is to be performed and the dose selected is 5 ABC units, the total dose of collagenase administered will be 5 ABC units. The concentration of collagenase stered to the area affected by enase is between about 50 ABC units/ml to about 2000 ABC units/ml. Collagenase can be administered in a volume per injection of about 0.5 ml or less. In r aspect, collagenase can be administered in a volume per injection of about 0.1 ml to about 0.5 ml. The total volume of collagenase injected can, for example, be between about 0.1 ml (when only a single ion site is used) to about 7 ml (for multiple sites of injections), and higher for larger size treatment areas. In one embodiment where the treatment area is about 80 cm2, the total volume injected is about 1 to about 5 ml, summed from 10 injections of between 0.1 ml and 0.5 ml.

Collagenase is an enzyme that has the specific ability to digest collagen. One commercial source of collagenase is from fermentation by Clostrz'dz'um histolytz'cum. In n aspects, the collagenase comprises a combination of purified Clostrz'dz'um histolytz'cum collagenase I and collagenase II. ably, the collagenase I and collagenase II are present in a mass ratio of about 1 to l. Collagenase AUX I has a single polypeptide chain consisting of approximately 1000 amino acids with a molecular weight of l 15 kDa. enase AUX II also has a single polypeptide chain consisting of about 1000 amino acids with a molecular weight of 110 kDa. Crude enase obtained from C. histolytz'cum can be purified by a variety of methods known to those skilled in the art, including, for example, heparin affinity chromatography, ammonium sulfate precipitation, hydroxylapatite chromatography, size exclusion chromatography, ion exchange chromatography, and metal chelation chromatography. s of purification of crude collagenase obtained from C. histolytz'cum are also described in US. Pat. No. 7,811,560, the contents of which are expressly orated herein by reference herein. As discussed above, an inj ectable formulation comprising C. histolytz'cum collagenase I and collagenase II is sold in the US. under the trade W0 2013/059619 PCT/U82012/061063 _ 8 _ name XIAFLEX® and is approved by the US. FDA for the treatment of Dupuytren’s contracture. The collagenase can, for example, be a parenteral lized product comprised of two collagenases in an approximate 1:1 mass ratio, Collagenase I (AUX-I, Clostridial type I collagenase) and Collagenase II I; Clostridial type II enase). Preferably, the collagenase comprises enase I and collagenase II have a mass ratio of about 1 to 1 and having a purity of at least about 95% by area as determined by reverse phase high performance liquid chromatography (as described, for example, in US. Pat. No. 7,811,560).

Collagenase compositions of the invention can also be prepared by mixing either a specific number of activity units or specific masses of the purified enzymes. Collagenase activity can be measured by the enzyme’s ability to hydrolyze either synthetic peptide or collagen substrate. Those skilled in the art will recognize that enzyme assays other than those disclosed herein may also be used to define and prepare functionally equivalent enzyme compositions.

It is understood that the terms "Collagenase I", "ABC I", "AUX I", "collagenase AUX I", and "collagenase ABC I" mean the same and can be used hangeably.

Similarly, the terms genase II", "ABC II", "AUX II", "collagenase AUX II", and "collagenase ABC II" refer to the same enzyme and can also be used interchangeably.

In certain onal embodiments, the collagenase administered according to a method described herein is a recombinant collagenase.

The collagenase is administered in a pharmaceutical composition comprising collagenase and a ceutically acceptable carrier or diluent. In some ments, the ition does not include a protease enzyme other than collagenase (other than a small or trace amount of proteolytic enzyme that may be present in the collagenase purified from a bacterial fermentation). In additional embodiments, the pharmaceutical composition does not include an enzyme other than collagenase (other than a small or trace amount of enzyme that may be present in the collagenase purified from a bacterial fermentation). The person of skill in the art will understand that a collagenase derived from a bacterial fermentation, even after purification, may contain small or trace amounts of impurities, including other enzymes, such as other protease enzymes. The small or trace amount of ty can, for example, be less than about 5%, less than about 4%, less than about 3%, less than about 2% or less than about 1% of the enase composition. In some embodiments, the small or trace amount of impurity can be less than about 1%, 2%, 3%, 4% or 5% by area, as ined by reverse W0 2013/059619 PCT/U82012/061063 _ 9 _ phase high performance liquid chromatography. In another aspect, the ceutical composition consists ially of collagenase and a pharmaceutically able carrier or diluent. As used herein, a pharmaceutically ition sting essentially of enase and a pharmaceutically acceptable carrier or diluent" is intended to exclude from the pharmaceutical compositions other protease s and hyaluronidase other than small or trace amounts as described above. In certain additional aspects, a composition "consisting essentially of collagenase" excludes from the compositions an enzyme other than collagenase. In yet r embodiment, the pharmaceutical composition consists of collagenase and a pharmaceutically acceptable salt thereof.

The method of treating or reducing EFP can further include the pre-treatment of the target area with a local anaesthetic agent.

In further aspects, the invention is directed to the treatment or reduction of EFP in a patient consisting essentially of administering one or a plurality injections of collagenase to an area affected by EFP n the dose of collagenase administered is between about 5 to about 200 ABC units and optionally, further wherein the concentration of collagenase is about 50 to about 2000 ABC units/ml. In yet an onal aspect, the invention is directed to the treatment or reduction of EFP in a patient consisting of administering a plurality of injections of collagenase wherein the dose of collagenase administered per injection is between about 5 to about 200 ABC units and optionally, further wherein the concentration of collagenase is about 50 to about 2000 ABC units/ml.

The ceutically acceptable carrier can be one or more liquid carriers or excipients appropriate for injection. As used herein, the term "pharmaceutically acceptable carrier or excipient" means a non-toxic, inert, liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials which can serve as pharmaceutically acceptable carriers are sugars such as e, glucose and e; es such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; glycols such as propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; ing agents such as ium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's on; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, perfiaming PCT/U82012/061063 _ 10 _ agents, preservatives and antioxidants can also be present in the composition, according to the nt of the ator. Injectable preparations, for example, sterile inj ectable aqueous or oleaginous suspensions, may be formulated ing to the known art using suitable dispersing or wetting agents and suspending agents. The e injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a on in 1, 3-butanediol.

Among the acceptable es and solvents that may be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a t or suspending medium. For this e any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables.

The inj ectable formulations can be ized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be ved or dispersed in sterile water or other sterile inj ectable medium prior to use. The sterile solutions can also be lyophilized for later use. In one embodiment, the pharmaceutical composition comprising collagenase is a lyophilized inj ectable composition formulated with lactose. In one embodiment each milligram of injectable collagenase is formulated with 1.9 mg of lactose. In another embodiment, each milligram of injection collagenase preferably has approximately 2800 SRC units and 51000 units measured with a y assay using a synthetic substrate, szPGGPA.

In r embodiment, the collagenase composition used according to a method of the invention is a lyophilized inj ectable composition formulated with sucrose, Tris at a pH level of about 8.0. For example, 1.0 mg of the drug substance of the invention is formulated in 60 mM sucrose, 10 mM Tris, at a pH of about 8.0 (this s to 20.5 mg/mL of sucrose and 1.21 mg/mL of Tris in the formulation buffer). Generally, a source of calcium is included in the ation, such as calcium chloride.

The invention will be better understood in connection with the following examples, which are intended as an illustration only and not limiting of the scope of the invention.

Various changes and modifications to the disclosed embodiments will be apparent to those d in the art and such changes and modifications may be made without departing from the spirit of the invention and the scope of the appended claims.

PCT/U82012/061063 _ 11 _ EXAMPLES Example 1: Effectiveness of Collagenase Clostridium Histolfiicum in lysing dermal collagen in gen minipigs Collagenase Clostridium Histolyticum (Auxilium Product Operation, Malvem, PA) is a parenteral lyophilized product comprised of two collagenases in an approximate l:l mass ratio, Collagenase I , idial type I collagenase) and Collagenase II (AUX-II; Clostridial type II collagenase). These collagenases are isolated and purified from the fermentation of Clostridium ytz'cum. The vehicle for reconstitution of the lyophilized product was saline (0.9% sodium chloride) with 0.03% (2 mM) calcium chloride. The vehicle for dilution and ation of the formulations described in more detail below was saline (0.9% sodium chloride for injection; Baxter Healthcare Corporation, Deerfield, IL) with 10 mM (013%) TRIZMA ® (Sigma Aldrich, Inc., St. Louis, MO), 60 mM (2.0%) sucrose (Sigma Aldrich, Inc., St. Louis, MO), and 2 mM calcium chloride (pH 8.0) ch Chemical Corporation, own, PA). lN HCl (hydrochloric acid) was used to bring the pH of the vehicle for dilution to 8.0. The vehicle for dilution was mixed throughout preparation, ng and dose administration procedures. The vehicle for dilution was then sterile-filtered using a 0.22-um PVDF syringe filter into a sterile vial and capped with a septum. The vehicle for dilution was prepared using aseptic technique within a laminar flow hood using sterilized glassware and utensils.

Dosing formulations were prepared at the test article (Collagenase Clostridium Histolyticum) concentrations indicated in the ing table: Table 1 Test Article Concentration a (mg/mL)/ Treatment Number ABC units/ml H 1 0.0015/ 8 .9 2 0.003/ 8 51.2 3 0.005/ 8 _ 12 _ 86.2 4 0.009/ 8 155.2 -7 0.015/ 8 258.6 8-9 0.03/ 8 517.2 0.07/ 8 1206.9 11 0.09/ 8 1551.7 12 0.15/ 8 2586.2 = The test article formulations were not adjusted for purity. = pH measurement using litmus paper.

The dosing formulations were prepared on the day of dosing. The lyophilized product was reconstituted using the vehicle for reconstitution to obtain a 2.5 mg/mL stock test article solution. The vehicle for on was used to dilute the stock test article solution and e the formulations to be used for dosing. The formulations were maintained on wet ice prior to, and during dosing. Formulations were prepared using aseptic que within a laminar flow hood using ized are and utensils.

Gottingen minipigs were used as the test system on this study. This species and breed of animal is recognized as appropriate for general toxicity studies and has been ed as a ical research model in a wide variety of disciplines. Swine exhibit many similarities with man in cardiovascular anatomy and physiology, digestive physiology, and integumentary structure and function. Because of the rity of the anatomy and physiology of the skin between swine and man, swine have become standard models for plastic surgery, wound healing, and dermal toxicity studies (Svendsen et al, , Scandinavian Journal ofLaboratory Animal Science 1998, 25 (supplement I):27-30).

Historically, the swine has been used in toxicological assessment of prospective therapeutics.

Gottingen minipigs (4 males and 3 females) were received in good health from Marshall BioResources, North Rose, NY. The animals were approximately 3 to 4 months old at receipt. Each animal ed one dose of all 12 treatments, for a total dose per animal of approximately 0.43 mg Collagenase Clostridium Histolyticum. The animals were approximately 4 months old at dose administration. Body weights ranged from 7185 g to 8646 g for the males and 9333 g to 9633 g for the females at dosing. Test article _ 13 _ formulations were administered to animals etized by telazol/xylazine on study day 0 by subcutaneous injection ). The day prior to injection, the designated areas for injection were clipped if necessary. Six injections were administered along the right and left lateral trunk of each animal using an appropriately sized syringe and needle (16-23 gauge). Animals were not dosed in the same site more than once. Each subcutaneous injection consisted of a different, randomly assigned treatment (combination of formulation concentration and dose volume). Injection sites were spaced sufficiently apart to prevent possible reactions from adjacent ion sites. The area immediately surrounding the site of test article deposition was marked using permanent marker and ed as needed. Individual injection sites were labeled. The selected route of administration for this study was aneous injection.

No drug-related histologic effects were detected in adipocytes, nerves, adnexal structures (hair follicles, sweat glands and sebaceous glands) or the overlying epidermis.

There were no consistent differences in collagen lysis between the sexes or n the animals euthanized at 24 or 48 hours post-dosing in the estimated extent of collagen lysis and the results are combined by gender for the 24 and 48 hour post-dosing necropsies in the table below. At concentrations less than 0.015 mg/mL, the extent of collagen lysis was generally dose sive. At 2 0.015 mg/mL the extent of collagen lysis was generally proportional to the dose volume ed as opposed to the total dose or formulation concentration (for example, test articles 7 and 8 represent the same dose given at a lower concentration and higher volume for test article 7).

Table 2 Total Dose (mg)/ Concentration Dose ABC Mean Extent of Collagen Lysis Test (mg/mL)/(ABC Volume units )a e units/ml (mL) Males Females Both 1 0.0015/ 0.2 0.0003/ 0.38 2.90 1 .64 .9 5.17 2 0.003/ 0.2 0.0006/ 2.15 1.77 1.96 51.2 10.3 3 0.005/ 0.2 0.001/ 1.81 1.84 1.82 86.2 17.2 0.009/ 0.2 0.0018/ 3.13 2.27 2.70 155.2 31.0 0.015/ 0.05 0.00075/ 1.89 3.04 2.47 258.6 12.9 0.015/ 0.1 0.0015/ 4.15 2.82 3.48 258.6 25.9 0.015/ 0.2 0.003/ 5.84 3.89 4.87 258.6 51.2 0.03/ 0.1 0.003/ 3.93 3.57 3.75 517.2 51.2 0.03/ 0.2 0.006/ 6.05 4.08 5.07 517.2 103.4 0.07/ 0.1 0.007/ 6.37 4.78 5.57 1206.9 120.7 11 0.09/ 0.1 0.009/ 5.50 4.60 5.05 1551.7 155.2 12 0.15/ 0.1 0.015/ 5.72 4.43 5.07 2586.2 258.6 a = For each gender, the mean extent of collagen 1ysis was ed for all three animals at the 24 and 48 hour necropsy als.

Collagenase Clostridium Histolyticum administered as single subcutaneous injections at trations ranging from 0.0015 to 0.15 mg/mL resulted in local swelling at sites treated with C011agenase Clostridium Histolyticum concentrations 20.015 mg/mL and collagen 1ysis (the expected pharmacologic effect of C011agenase Clostridium Histolyticum) at all doses, dose volumes, and formulation concentrations in this study. The minimally effective dose in this study was 0.0003 mg protein and the minimally effective concentration W0 2013/059619 PCT/U82012/061063 _ 15 _ was 0.0015 mg/mL. At concentrations less than 0.015 mg/mL, a dose response generally was apparent for the extent of collagen lysis. At concentrations 20.015 mg/mL, the extent of effective en lysis reflected the dose volume given more than the total dose or formulation tration.

Collagen lysis was accompanied consistently by a number of secondary changes.

These changes included the following: hemorrhage and/or acute inflammation seen consistently at all effective dose levels; necrosis of the muscle fibers of the panniculus camosis at 20.003 mg/mL (total doses 2 0.0006 mg protein); perivascular and intramural edema, neovascularization/flbrosis, vascular necrosis, and/or thrombosis seen sporadically at concentrations 20.009 mg/mL (total doses 20.0018 mg n); and al ural hemorrhage seen sporadically at formulation concentrations 20.030 mg/mL (total doses .003 mg protein). There were no Collagenase Clostridium Histolyticum-mediated effects on ytes, nerves, adnexal structures or the overlying epidermis.

Results from this study showed some degree of histologically detectable collagen lysis of the dermal septa at all Collagenase Clostridium Histolyticum dose concentrations; however, more areas of complete lysis of dermal septa were seen at concentrations 20.015 mg/mL. In this study, there were no Collagenase Clostridium Histolyticum mediated effects on adipocytes, nerves, adnexal skin structures or the overlying epidermis. Local effects of Collagenase Clostridium Histolyticum (hemorrhage and/or acute inflammation) at each concentration were ed upon gross and/or microscopic examination at necropsy. There were no consistent differences in collagen lysis between the sexes or between the animals euthanized at 24 or 48 hours post-dosing in the estimated extent of en lysis.

At concentrations effective in the te lysis of the dermal septae, dose and volume-dependent collagen lysis was noted to occur within a diameter of approximately 2.5 cm in the minipig study.

PCT/U82012/061063 _ 16 _ Example 2: Phase 1b, open-label= dose-escalation and pharmacokinetic study for the ent of EFP The objectives of this study are to assess the safety, effectiveness, pharmacokinetics, and immunogenicity of Collagenase Clostridium Histolyticum at increasing total doses in an 80 cm2 area, ranging from 0.0029 mg to 0.116 mg (50 to 2000 ABC units) and increasing concentrations ranging from 0.0029 mg/mL to 0.116 mg/mL (50 to 2000 ABC units per mL) in the ent of adult women with EFP.

Based on the findings discussed above in the minipig study (Example 1), the ion template for the Phase 1 clinical study is designed to allow for a distance of approximately 2.5 cm between injections. This distance is ed to enable adequate distribution and activity of Collagenase Clostridium Histolyticum within the 8 cm x 10 cm area of EFP without significant gaps or overlap within the treatment area. In an attempt to determine the l dose for the treatment of EFP (for example, efficacious with minimal local adverse s), dose selection was made following consideration of the ble safety profile of Collagenase Clostridium Histolyticum to date both in clinical development and al practice as well as on data from the minipig study. As a result, a starting dose of 0.0029 mg injected as 10 separate 9 mg doses within the 8 cm x 10 cm target EFP area at a concentration of 0.0029 mg/mL is proposed for the Phase 1 study.

This study is a Phase lb, open-label, dose-escalation and pharmacokinetic study.

During the screening visit, while the subject is standing, the investigator or qualified designee will examine the left and right k and the left and right thigh and select a quadrant that has a photonumeric EFP severity scale (CSS) score of Z 10 representing moderate to severe EFP severity (Hexsel et al., 2009). The investigator or qualified designee will identify an area of EFP within the selected quadrant that is at least 8 cm x 10 cm (i.e., target EFP area) and is suitable for treatment (i.e., that is on the lateral upper aspect of the thigh or within the buttock and does not involve the gluteal fold). The target EFP area must be evident when the subject is standing, without the use of any manipulation such as skin pinching or muscle contraction. Each subject will be ed for study eligibility within 21 days before injection of study drug on Day 1.

W0 2013/059619 PCT/U82012/061063 _ 17 _ In this study, 63 subjects will each receive 10 concurrent equal volume injections of Collagenase Clostridium yticum within the target EFP area. Following screening and determination of study eligibility, subjects will be assigned sequentially to Cohorts l, 2, 3, and 4 (Table 3). The first nine subjects will be assigned to Cohort l (1 mL total volume/target EFP area). Within each of following Cohorts 2 to 4, the first nine subjects in each cohort will be assigned to the 5 mL total volume/target EFP area followed by the next nine subjects who will be assigned to the 1 mL total volume/target EFP area. Dosing will start with Cohort l. Dosing in Cohorts 2 and 3 will not begin until the safety of subjects in Cohort 1 has been evaluated by the safety monitoring tee (SMC). Dosing in Cohort 4 will not begin until the safety of ts in Cohorts 2 and 3 has been evaluated by the SMC.

The doses proposed to treat an 8 cm X 10 cm area of EFP represent between 0.5% (0.0029 mg) and 20% (0. 1 16 mg) of the dose used in a single injection for Dupuytren’s contracture at a concentration that is between 0. 1% 9 mg/mL) and 5% (0. l 16 mg/mL) of the concentration used in the approved product for Dupuytren’s contracture.

Table 3: Study Drug Assignment by Cohort EFP Dose/ EFP Concentration Target EFP Area as a t of the Dose CCH/ Volume/ as a Percent of the Approved Dupuytren’s Target Target Approved Dupuytren’s Concentration Cohort EFP Areaa EFP Areaa tration Dose (0.58 m_) (2.3 m_/mL) (50 U)b lmL 250U 5 mL (250 U) 1 mL (250 U/mL) 3. _- 750U 5 mL (750 U) 1 mL (750 U/mL) (2000 U) 5 mL (400 U/mL) a A total of 10 single injections at the target injection sites across the 8 cm X 10 cm target EFP area.

CCH is Collagenase Clostridium histolyticum b U is ABC units _ 18 _ The components of enase Clostridium Histolyticum are: mixed collagenase AUX-I and AUX-II, 10 mM tris, 60 mM sucrose. The components of Collagenase Clostridium Histolyticum e Diluent A for reconstitution are: 0.03% (2 mM) calcium chloride (CaCL) in 0.9% (154 mM) sodium chloride (NaCL) solution, pH 6.0-7.0, is supplied as a terminally-sterilized liquid at 3.0 mL per vial. The components of sterile enase Clostridium Histolyticum buffered sterile Diluent B for filrther dilution are: 0.03% (2 mM) calcium chloride and 0.12% (10 mM) tromethamine (TRIS) in 0.9% (154 mM) sodium chloride, pH 8.0 chloride is supplied as a terminally-sterilized liquid at 3.0 mL per vial. After reconstitution with Diluent A and fiarther dilution with Diluent B, the A4500 on can be kept at room ature (20° to 25°C/68° to 77°F) for up to one hour or refrigerated at 2° to 8°C (36° to 46°F) for up to 4 hours prior to administration.

An injection template will be made of a thin clear material. The 8 cm x 10 cm injection template will be pre-stamped with the diagram and injection sites shown in Each of the black dots within the octagon represents an ion site. The encircled ‘X’ represents the injection site of the central dimple (i.e., the area of the deepest depression in the target area (. Each black dot (including the site of the central dimple and the four comers) will be cut-out to enable the investigator to mark the target EFP area as needed.

Each dot within the octagon shown in represents an injection site. The X within the circle represents the injection site to the ‘central dimple’. The four comers are labeled as upper right (UR), lower right (LR), upper left (UL), and lower left (LL).

During the screening visit, while the subject is standing, the investigator or qualified designee will e the left and right buttock and the left and right posterior upper thigh and select a quadrant that has moderate to severe EFP (CSS score of 210). The investigator or qualified designee will identify an area of EFP within the ed nt that is at least 8 cm x 10 cm (referred to in this example as the target EFP area) and is suitable for treatment (for example, is within posterior upper thigh or within the buttock and does not e the gluteal fold). The target EFP area must also be evident when the subject is standing, without the use of any manipulation (such as skin pinching or muscle contraction).

PCT/U82012/061063 _ 19 _ The investigator will then place the injection template over the target EFP area (while the subject remains standing) and on the template encircled ‘X’ over the center of the deepest depression (for example, the central dimple) in the target area. The investigator will use a surgical marker and mark the subject’s skin at two comers of the template. The investigator will remove the template and record which two comers of the te were marked (e. g., upper right, lower right, upper left, lower left). The investigator will use a tape measure to measure as follows: 1. Identify the midline of the upper thigh and buttock starting from the center of the popliteal fossa (. 2. Identify the line that is perpendicular to the midline and goes through the first template comer mark (as ed in [Line BC]). Measure distance between Points B and C (record distance). 3. Measure the distance from Point A to Point B as depicted in (record distance). 4. Repeat Steps 2 and 3 for measurement of the second template comer mark ( [Points A, D, and E]).

Each recorded measurement will be later used to relocate the 8 cm x 10 cm target EFP area before injection and before each efficacy evaluation time point.

On Day 1, after the injection site has been identified, marked (as described above), photographed, and the pre-inj ection efficacy evaluations have been ted, the t will be positioned prone on the ation table so that the entire 8 cm x 10 cm target EFP area with the previously marked injection sites is visible and assessable to the igator.

The injection site area should be prepped with an appropriate antiseptic such as alcohol.

Using a previously prepared 5mL or 1 mL syringe (depending on cohort assignment) with a 30 gauge 14 inch needle, the investigator will administer a dose of either 0.5 mL or 0.1 mL of Collagenase idium yticum into each of the 10 injection sites. At each of the 10 sites, study drug will be injected perpendicular to the subject’s skin to a depth of 14 inch (~7 mm).

The investigator will administer study drug in a sequence that s each of the 10 sites receives a single 0.5 mL or 0.1 mL injection of Collagenase Clostridium Histolyticum.

Following the tenth injection, the maximum permissible volume of study drug will have been administered (5 mL or 1 mL). Any injectate on the surface of an injection site following injection stive of extravasation) will be noted and the associated injection location will PCT/U82012/061063 be recorded. No local massage or palpation will be performed subsequent to injection of study drug.

The following primary endpoints will be ted at Day 90: o Investigator global aesthetic ement scale assessment of the target EFP area; 0 Subject global aesthetic improvement scale assessment of the target EFP area; and o A responder analysis based on proportion of subjects with a Z 30% ement from baseline in surface contour standard deviation of the target EFP area based on 3-D digital photography.

While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that s s in form and details may be made therein Without departing from the scope of the invention encompassed by the appended claims.

Claims (18)

CLAIMS What is claimed is:

1. Use of collagenase for the ation of a medicament for ng or reducing edematous fibrosclerotic panniculopathy (EFP) in a t, wherein said medicament is adapted for administration of a plurality of subdermal injections of enase comprising collagenase I and collagenase II in a 1:1 mass ratio with a specific activity of 10,000 ABC units per 0.58 mg of collagenase to an area affected by the EFP, wherein the dose of collagenase per injection is between about 5 to about 200 ABC units and the injection sites are about 1 cm to about 4 cm from one another.

2. The use of claim 1, wherein the number of subdermal injections depends on the size of the area to be treated.

3. The use of claim 1, wherein the concentration for administration is between about 50 to about 2000 ABC units per milliliter.

4. The use of any one of claims 1 to 3, wherein each ion of collagenase is formulated for stration in a volume of about 0.5 ml or less.

5. The use of any one of claims 1 to 4, wherein the total dose of collagenase for administration is between about 5 to about 2000 ABC units.

6. The use of any one of claims 1 to 5, wherein the dose of collagenase per injection is between about 5 to about 100 ABC units.

7. The use of any one of claims 1 to 5, wherein the dose of collagenase per injection is between about 5 to about 50 ABC units.

8. The use of any one of claims 1 to 7, wherein the collagenase is present in a pharmaceutical composition consisting essentially of collagenase and a pharmaceutically acceptable carrier.

9. The use of any one of claims 1 to 7, wherein the collagenase is present in a pharmaceutical composition consisting of collagenase and a pharmaceutically acceptable carrier.

10. The use of any one of claims 1 to 7, wherein at least two injections of collagenase are formulated for administration to two ion sites within the affected area.

11. The use of claim 10, wherein at least five injections of collagenase are formulated for administration to five ion sites within the affected area.

12. The use of claim 11, wherein at least ten injections of collagenase are formulated for administration to ten injection sites within the affected area.

13. The use of any of the ing claims, wherein the affected area of EFP has an area of about 1 cm2 to about 200 cm2.

14. The use of any one of the previous claims, wherein the distance between injection sites is about 2 to about 3 cm.

15. The use of claim 13, wherein the area affected by EFP has a length of about 10 cm and width of about 8 cm.

16. The use of claim 15, wherein there is a distance of about 2.5 cm between injection sites.

17. The use of any one of the previous claims, wherein each injection has a volume of about 0.5

18. The use of any one of any one of the previous claims, n each injection has a volume of about 0.1 ml.