ME02858B - Formulacija za anti- 4 7 antitelo - Google Patents
Formulacija za anti- 4 7 antiteloInfo
- Publication number
- ME02858B ME02858B MEP-2017-227A MEP2017227A ME02858B ME 02858 B ME02858 B ME 02858B ME P2017227 A MEP2017227 A ME P2017227A ME 02858 B ME02858 B ME 02858B
- Authority
- ME
- Montenegro
- Prior art keywords
- seq
- stable liquid
- pharmaceutical formulation
- liquid pharmaceutical
- formulation according
- Prior art date
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39591—Stabilisation, fragmentation
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/08—Solutions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2839—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the integrin superfamily
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/54—Medicinal preparations containing antigens or antibodies characterised by the route of administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/545—Medicinal preparations containing antigens or antibodies characterised by the dose, timing or administration schedule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Diabetes (AREA)
- Virology (AREA)
- Dermatology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
Claims (31)
1. Stabilna tečna farmaceutska formulacija koja obuhvata anti-α4β7 antitelo, citrat, i najmanje jednu slobodnu aminokiselinu, pri čemu anti-α4β7 antitelo obuhvata varijabilan region lakog lanca koji obuhvata region 1 koji određuje komplementarnost (CDR1) koji obuhvata SEQ ID NO:11, CDR2 koji obuhvata SEQ ID NO:12, i CDR3 koji obuhvata SEQ ID NO:13, i obuhvata varijabilan region teškog lanca koji obuhvata CDR1 koji obuhvata SEQ ID NO:8, CDR2 koji obuhvata SEQ ID NO:9, i CDR3 koji obuhvata SEQ ID NO:10.
2. Stabilna tečna farmaceutska formulacija prema zahtevu 1, u kojoj je molarni odnos anti-α4β7 antitela prema citratu oko 1:4 do oko 1:100.
3. Stabilna tečna farmaceutska formulacija prema zahtevu 1 ili 2, u kojoj je pomenuta slobodna aminokiselina odabrana iz grupe koju čine histidin, alanin, arginin, glicin, glutaminska kiselina i njihove kombinacije.
4. Stabilna tečna formulacija prema bilo kom od prethodnih zahteva, koja dalje obuhvata neki surfaktant.
5. Stabilna tečna farmaceutska formulacija prema zahtevu 4, u kojoj je molarni odnos citrata prema surfaktantu oko 3:1 do oko 156:1.
6. Stabilna tečna formulacija prema zahtevu 4 ili 5, u kojoj surfaktant predstavlja polisorbat 20, polisorbat 80, poloksamer i njihove kombinacije.
7. Stabilna tečna formulacija prema zahtevu 6, u kojoj surfaktant predstavlja polisorbat 80, a koncentracija polisorbata 80 je 0,01% do 0,5%.
8. Stabilna tečna farmaceutska formulacija prema bilo kom od zahteva 1-7, u kojoj je koncentracija citrata 5 mM do 50 mM.
9. Stabilna tečna farmaceutska formulacija koja obuhvata najmanje oko 60 mg/ml do oko 190 mg/ml anti-α4β7 antitela, antioksidans ili helator, i najmanje jednu slobodnu aminokiselinu, pri čemu anti-α4β7 antitelo obuhvata varijabilan region lakog lanca koji obuhvata region 1 koji određuje komplementarnost (CDR1) koji obuhvata SEQ ID NO:11, CDR2 koji obuhvata SEQ ID NO:12, i CDR3 koji obuhvata SEQ ID NO:13, i obuhvata varijabilan region teškog lanca koji obuhvata CDR1 koji obuhvata SEQ ID NO:8, CDR2 koji obuhvata SEQ ID NO:9, i CDR3 koji obuhvata SEQ ID NO:10.
10. Stabilna tečna farmaceutska formulacija koja obuhvata anti-α4β7 antitelo, antioksidans ili helator, i najmanje jednu slobodnu aminokiselinu, pri čemu anti-α4β7 antitelo obuhvata varijabilan region lakog lanca koji obuhvata region1 koji određuje komplementarnost (CDR1) koji obuhvata SEQ ID NO:11, CDR2 koji obuhvata SEQ ID NO:12, i CDR3 koji obuhvata SEQ ID NO:13, i obuhvata varijabilan region teškog lanca koji obuhvata CDR1 koji obuhvata SEQ ID NO:8, CDR2 koji obuhvata SEQ ID NO:9, i CDR3 koji obuhvata SEQ ID NO:10, i gde formulacija ima pH od 6,1 do 7,0.
11. Stabilna tečna farmaceutska formulacija prema zahtevu 9 ili 10, koja obuhvata oko 150 mg/ml do oko 180 mg/ml anti-α4β7 antitela.
12. Stabilna tečna farmaceutska formulacija prema zahtevu 9 ili 10, u kojoj antioksidans ili helator predstavlja citrat ili EDTA.
13. Stabilna tečna farmaceutska formulacija prema zahtevu 12, u kojoj antioksidans ili helator predstavlja citrat.
14. Stabilna tečna farmaceutska formulacija prema zahtevu 13, u kojoj je koncentracija citrata 5 mM do 50 mM.
15. Stabilna tečna farmaceutska formulacija prema bilo kom od zahteva 9-15, koja dalje obuhvata neki surfaktant.
16. Stabilna tečna farmaceutska formulacija prema zahtevu 15, u kojoj je molarni odnos surfaktant:antitelo od oko 0,7:1 do oko 2,0:1.
17. Stabilna tečna farmaceutska formulacija prema zahtevu 15, u kojoj je molarni odnos antioksidansa ili helatora prema surfaktantu oko 3:1 do oko 156:1.
18. Stabilna tečna farmaceutska formulacija prema zahtevu 15, u kojoj surfaktant predstavlja polisorbat 20, polisorbat 80, poloksamer i njihove kombinacije.
19. Stabilna tečna farmaceutska formulacija prema zahtevu 18, u kojoj surfaktant predstavlja polisorbat 80, a koncentracija polisorbata 80 je 0,01% do 0,5%.
20. Stabilna tečna farmaceutska formulacija prema zahtevu 9 ili 10, koja obuhvata anti-α4β7 antitelo, citrat, histidin, arginin, i polisorbat 80, pri čemu anti-α4β7 antitelo obuhvata varijabilan region lakog lanca koji obuhvata region1 koji određuje komplementarnost (CDR1) koji obuhvata SEQ ID NO:11, CDR2 koji obuhvata SEQ ID NO:12, i CDR3 koji obuhvata SEQ ID NO:13, i obuhvata varijabilan region teškog lanca koji obuhvata CDR1 koji obuhvata SEQ ID NO:8, CDR2 koji obuhvata SEQ ID NO:9, i CDR3 koji obuhvata SEQ ID NO:10.
21. Stabilna tečna farmaceutska formulacija prema zahtevu 20, u kojoj je koncentracija anti-α4β7 antitela najmanje oko 140 mg/ml.
22. Stabilna tečna farmaceutska formulacija prema zahtevu 20 ili 21, u kojoj je koncentracija histidina 10 mM do 75 mM.
23. Stabilna tečna farmaceutska formulacija prema bilo kom od zahteva 20-21, u kojoj je koncentracija arginina 50 mM do 150 mM.
24. Stabilna tečna farmaceutska formulacija prema bilo kom od zahteva 20 - 23, u kojoj je koncentracija citrata 5 mM do 50 mM.
25. Stabilna tečna farmaceutska formulacija prema bilo kom od zahteva 1-24, u kojoj antitelo obuhvata varijabilan region teškog lanca koji obuhvata aminokiseline 20-140 iz SEQ ID NO: 2 i varijabilan region lakog lanca koji obuhvata aminokiseline 20-131 iz SEQ ID NO:4 ili aminokiseline 21-132 iz SEQ ID NO:5.
26. Stabilna tečna farmaceutska formulacija prema bilo kom od prethodnih zahteva, u kojoj pomenuto antitelo predstavlja vedolizumab.
27. Proizvod proizvodnje koji obuhvata kontejner, stabilnu tečnu farmaceutsku formulaciju prema bilo kom od zahteva 1-26, i instrukcije za njenu upotrebu.
28. Proizvod prema zahtevu 27, u kom pomenuta stabilna tečna farmaceutska formulacija obuhvata 108 mg antitela.
29. Proizvod prema zahtevu 27, pri čemu proizvod predstavlja prethodno napunjen špric.
30. Stabilna tečna farmaceutska formulacija prema bilo kom od zahteva 1-26 ili proizvod proizvodnje prema bilo kom od zahteva 27 do 29 za upotrebu u lečenju zapaljenske bolesti creva.
31. Stabilna tečna farmaceutska formulacija ili proizvod proizvodnje prema zahtevu 30, pri čemu zapaljenska bolest creva predstavlja Kronovu bolest ili ulcerozni kolitis.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161481522P | 2011-05-02 | 2011-05-02 | |
| US201161544054P | 2011-10-06 | 2011-10-06 | |
| PCT/US2012/036069 WO2012151247A2 (en) | 2011-05-02 | 2012-05-02 | FORMULATION FOR ANTI-α4β7 ANTIBODY |
| EP12722973.0A EP2704742B1 (en) | 2011-05-02 | 2012-05-02 | Formulation for anti- 4 7 antibody |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02858B true ME02858B (me) | 2018-04-20 |
Family
ID=46147702
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2017-227A ME02858B (me) | 2011-05-02 | 2012-05-02 | Formulacija za anti- 4 7 antitelo |
Country Status (38)
| Country | Link |
|---|---|
| US (7) | US10040855B2 (me) |
| EP (5) | EP3311834A1 (me) |
| JP (6) | JP6190359B2 (me) |
| KR (8) | KR101884406B1 (me) |
| CN (4) | CN108969469A (me) |
| AR (1) | AR086238A1 (me) |
| AU (5) | AU2012250872B2 (me) |
| CA (2) | CA3051418C (me) |
| CL (3) | CL2013003145A1 (me) |
| CO (1) | CO6801648A2 (me) |
| CR (1) | CR20130556A (me) |
| CY (1) | CY1119436T1 (me) |
| DK (1) | DK2704742T3 (me) |
| DO (1) | DOP2013000252A (me) |
| EA (1) | EA032625B1 (me) |
| EC (1) | ECSP22046340A (me) |
| ES (1) | ES2646717T3 (me) |
| GE (2) | GEAP201813302A (me) |
| HK (1) | HK1253911A1 (me) |
| HR (1) | HRP20171457T1 (me) |
| HU (1) | HUE036664T2 (me) |
| IL (6) | IL274846B2 (me) |
| LT (1) | LT2704742T (me) |
| ME (1) | ME02858B (me) |
| MX (4) | MX354101B (me) |
| MY (1) | MY188820A (me) |
| PE (1) | PE20141672A1 (me) |
| PH (3) | PH12013502237A1 (me) |
| PL (1) | PL2704742T3 (me) |
| PT (1) | PT2704742T (me) |
| RS (1) | RS56429B1 (me) |
| SG (1) | SG194730A1 (me) |
| SI (1) | SI2704742T1 (me) |
| SM (1) | SMT201700515T1 (me) |
| TW (5) | TWI723339B (me) |
| UY (1) | UY34054A (me) |
| WO (1) | WO2012151247A2 (me) |
| ZA (2) | ZA201308168B (me) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO3672B1 (ar) | 2008-12-15 | 2020-08-27 | Regeneron Pharma | أجسام مضادة بشرية عالية التفاعل الكيماوي بالنسبة لإنزيم سبتيليسين كنفرتيز بروبروتين / كيكسين نوع 9 (pcsk9). |
| ES2688093T3 (es) | 2010-01-06 | 2018-10-30 | Dyax Corp. | Proteínas de unión a calicreína plasmática |
| MY158130A (en) * | 2010-10-06 | 2016-08-30 | Regeneron Pharma | Stabilized formulations containing anti-interleukin-4 receptor )il-4r) antibodies |
| KR102502293B1 (ko) | 2011-01-06 | 2023-02-21 | 다케다 파머수티컬 컴패니 리미티드 | 혈장 칼리크레인 결합 단백질 |
| PH12013501576A1 (en) | 2011-01-28 | 2013-09-30 | Sanofi Biotechnology | Pharmaceutical compositions comprising human antibodies to pcsk9 |
| UA116189C2 (uk) | 2011-05-02 | 2018-02-26 | Мілленніум Фармасьютікалз, Інк. | КОМПОЗИЦІЯ АНТИ-α4β7 АНТИТІЛА |
| AU2012250872B2 (en) * | 2011-05-02 | 2017-07-13 | Millennium Pharmaceuticals, Inc. | Formulation for anti-alpha4beta7 antibody |
| WO2013006810A1 (en) | 2011-07-06 | 2013-01-10 | Nestec Sa | Assays for detecting neutralizing autoantibodies to biologic therapy with tnf alpha |
| AR087305A1 (es) | 2011-07-28 | 2014-03-12 | Regeneron Pharma | Formulaciones estabilizadas que contienen anticuerpos anti-pcsk9, metodo de preparacion y kit |
| US9764093B2 (en) * | 2012-11-30 | 2017-09-19 | Sio2 Medical Products, Inc. | Controlling the uniformity of PECVD deposition |
| CA3208188A1 (en) | 2013-03-15 | 2014-09-25 | Takeda Pharmaceutical Company Limited | Anti-plasma kallikrein antibodies |
| US10857090B2 (en) * | 2013-07-05 | 2020-12-08 | Stellar Biome Inc. | Oral compositions |
| WO2015080513A1 (en) * | 2013-11-29 | 2015-06-04 | Hanwha Chemical Corporation | A liquid formulation of a fusion protein comprising tnfr and fc region |
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