AR080428A1 - Formulaciones liquidas estabilizadas contentivas de anticuerpos - Google Patents
Formulaciones liquidas estabilizadas contentivas de anticuerposInfo
- Publication number
- AR080428A1 AR080428A1 ARP110100185A ARP110100185A AR080428A1 AR 080428 A1 AR080428 A1 AR 080428A1 AR P110100185 A ARP110100185 A AR P110100185A AR P110100185 A ARP110100185 A AR P110100185A AR 080428 A1 AR080428 A1 AR 080428A1
- Authority
- AR
- Argentina
- Prior art keywords
- formulation according
- formulation
- antibody
- buffer
- hydroxymethyl
- Prior art date
Links
Classifications
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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
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- 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
-
- 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
- A61K47/16—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
-
- 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
-
- 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
- A61K9/08—Solutions
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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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- 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 [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/24—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
- C07K16/244—Interleukins [IL]
- C07K16/248—IL-6
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Dermatology (AREA)
- Organic Chemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicinal Preparation (AREA)
- Peptides Or Proteins (AREA)
Abstract
Un objetivo de la presente es proveer formulaciones estables contentivas de anticuerpos que sean adecuadas para la administracion subcutánea en las cuales se haya suprimido la formacion de agregados durante el almacenamiento por largos períodos. Los autores de la presente descubrieron que se logra un efecto estabilizador significativo al usar un amino ácido acídico, ácido aspártico o ácido glutámico como especies contraionicas en buffers de histidina o tris(hidroximetil)aminometano, específicamente usando un buffer de histidina-aspartato o de histidina-glutamato, o tris(hidroximetil)aminometano-aspartato o tris(hidroximetil) aminometano-glutamato como buffer. Reivindicacion 7: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 6 que sustancialmente no comprende ion cloruro e ion acetato. Reivindicacion 8: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 7 que adicionalmente comprende un azucar. Reivindicacion 9: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 8 en la que el anticuerpo es un anticuerpo humanizado o un anticuerpo humano. Reivindicacion 10: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 9 en la que el anticuerpo ha sido modificado para tener un punto isoeléctrico (pI) de 5 a 8. Reivindicacion 12: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 10 en la que la concentracion del anticuerpo es de 50 a 250 mg/ml. Reivindicacion 13: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 12 en la que la formulacion es líquida. Reivindicacion 17: La formulacion de acuerdo a cualquiera de las reivindicaciones 13 a la 16 y que esté congelada entre -30°C y -10°C. Reivindicacion 18: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 12 y que la formulacion sea una formulacion liofilizada. Reivindicacion 21: La formulacion de acuerdo a cualquiera de las reivindicaciones 1 a la 20 en la cual el anticuerpo es un anticuerpo del receptor anti-IL-6. Reivindicacion 22: La formulacion de acuerdo a cualquiera de las reivindicaciones 2, 4, y 7 a la 21 en la cual el buffer comprende sustancialmente solo aminoácidos. Reivindicacion 24: Un método para suprimir la formacion de agregado durante el almacenamiento congelado de una formulacion altamente concentrada contentiva de anticuerpos usando ácido aspártico o ácido glutámico como especie contraionica a un buffer de la formulacion.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010010060 | 2010-01-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR080428A1 true AR080428A1 (es) | 2012-04-11 |
Family
ID=44306888
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP110100185A AR080428A1 (es) | 2010-01-20 | 2011-01-19 | Formulaciones liquidas estabilizadas contentivas de anticuerpos |
| ARP210101446A AR122198A2 (es) | 2010-01-20 | 2021-05-28 | Formulaciones líquidas estabilizadas contentivas de anticuerpos |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP210101446A AR122198A2 (es) | 2010-01-20 | 2021-05-28 | Formulaciones líquidas estabilizadas contentivas de anticuerpos |
Country Status (22)
| Country | Link |
|---|---|
| US (3) | US10022319B2 (es) |
| EP (4) | EP3892292B1 (es) |
| JP (2) | JP5939799B2 (es) |
| KR (5) | KR102391571B1 (es) |
| CN (2) | CN105944099B (es) |
| AR (2) | AR080428A1 (es) |
| AU (5) | AU2011208075B2 (es) |
| BR (1) | BR112012018023A2 (es) |
| CA (2) | CA2786981C (es) |
| DK (1) | DK2526963T3 (es) |
| ES (2) | ES2985395T3 (es) |
| IL (3) | IL296486A (es) |
| MX (1) | MX349560B (es) |
| MY (1) | MY185867A (es) |
| NZ (1) | NZ601374A (es) |
| PL (2) | PL2526963T3 (es) |
| RU (1) | RU2653447C2 (es) |
| SG (2) | SG182517A1 (es) |
| TR (1) | TR201807401T4 (es) |
| TW (2) | TWI609698B (es) |
| WO (1) | WO2011090088A1 (es) |
| ZA (1) | ZA201205446B (es) |
Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2401040A (en) | 2003-04-28 | 2004-11-03 | Chugai Pharmaceutical Co Ltd | Method for treating interleukin-6 related diseases |
| AU2006232287B2 (en) | 2005-03-31 | 2011-10-06 | Chugai Seiyaku Kabushiki Kaisha | Methods for producing polypeptides by regulating polypeptide association |
| CN104761637B (zh) | 2006-03-31 | 2021-10-15 | 中外制药株式会社 | 调控抗体血液动力学的方法 |
| EP2009101B1 (en) | 2006-03-31 | 2017-10-25 | Chugai Seiyaku Kabushiki Kaisha | Antibody modification method for purifying bispecific antibody |
| ES2595638T3 (es) | 2007-09-26 | 2017-01-02 | Chugai Seiyaku Kabushiki Kaisha | Método para modificar el punto isoeléctrico de un anticuerpo mediante la sustitución de aminoácidos en una CDR |
| PE20091174A1 (es) † | 2007-12-27 | 2009-08-03 | Chugai Pharmaceutical Co Ltd | Formulacion liquida con contenido de alta concentracion de anticuerpo |
| SI2493922T1 (sl) | 2009-10-26 | 2017-06-30 | F. Hoffmann-La Roche Ag | Postopek za proizvodnjo glikoziliranega imunoglobulina |
| AR080428A1 (es) | 2010-01-20 | 2012-04-11 | Chugai Pharmaceutical Co Ltd | Formulaciones liquidas estabilizadas contentivas de anticuerpos |
| KR20190120439A (ko) | 2010-11-08 | 2019-10-23 | 제넨테크, 인크. | 피하 투여용 항―il―6 수용체 항체 |
| TWI452136B (zh) | 2010-11-17 | 2014-09-11 | 中外製藥股份有限公司 | A multiple specific antigen-binding molecule that replaces the function of Factor VIII in blood coagulation |
| WO2013012022A1 (ja) * | 2011-07-19 | 2013-01-24 | 中外製薬株式会社 | アルギニンアミドまたはその類似化合物を含む安定なタンパク質含有製剤 |
| HRP20250713T8 (hr) | 2011-09-01 | 2025-10-24 | Chugai Seiyaku Kabushiki Kaisha | Postupak priprave pripravka koji sadrži visoko koncentrirana protutijela ultrafiltriranjem |
| EP2834262B1 (en) * | 2012-04-04 | 2020-09-02 | Polaris Group | Composition comprising pegylated arginine deiminase |
| US9969794B2 (en) | 2012-05-10 | 2018-05-15 | Visterra, Inc. | HA binding agents |
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| EP2727602A1 (en) * | 2012-10-31 | 2014-05-07 | Takeda GmbH | Method for preparation of a high concentration liquid formulation of an antibody |
| UA117466C2 (uk) | 2012-12-13 | 2018-08-10 | Мерк Шарп Енд Доме Корп. | СТАБІЛЬНИЙ СКЛАД У ВИГЛЯДІ РОЗЧИНУ АНТИТІЛА ДО IL-23p19 |
| HUE056580T2 (hu) | 2013-05-30 | 2022-02-28 | Kiniksa Pharmaceuticals Ltd | Onkosztatin-M-receptor antigénjét kötõ fehérjék |
| ES2881306T3 (es) | 2013-09-27 | 2021-11-29 | Chugai Pharmaceutical Co Ltd | Método para la producción de heteromultímeros de polipéptidos |
| WO2015080513A1 (en) * | 2013-11-29 | 2015-06-04 | Hanwha Chemical Corporation | A liquid formulation of a fusion protein comprising tnfr and fc region |
| CA2942546C (en) * | 2014-03-17 | 2022-11-22 | Mitsubishi Tanabe Pharma Corporation | Antibody-fynomer conjugates |
| TWI831106B (zh) | 2014-06-20 | 2024-02-01 | 日商中外製藥股份有限公司 | 用於因第viii凝血因子及/或活化的第viii凝血因子的活性降低或欠缺而發病及/或進展的疾病之預防及/或治療之醫藥組成物 |
| TWI700300B (zh) | 2014-09-26 | 2020-08-01 | 日商中外製藥股份有限公司 | 中和具有第viii凝血因子(fviii)機能替代活性的物質之抗體 |
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| JP7082484B2 (ja) | 2015-04-01 | 2022-06-08 | 中外製薬株式会社 | ポリペプチド異種多量体の製造方法 |
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| AU2016381992B2 (en) | 2015-12-28 | 2024-01-04 | Chugai Seiyaku Kabushiki Kaisha | Method for promoting efficiency of purification of Fc region-containing polypeptide |
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| PL3509637T3 (pl) | 2016-09-06 | 2025-03-10 | Chugai Seiyaku Kabushiki Kaisha | Sposoby zastosowania dwuswoistego przeciwciała, które rozpoznaje czynnik krzepnięcia IX i/lub aktywowany czynnik krzepnięcia IX oraz czynnik krzepnięcia X i/lub aktywowany czynnik krzepnięcia X |
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2016
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- 2016-07-08 AU AU2016204729A patent/AU2016204729A1/en not_active Abandoned
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2018
- 2018-03-21 AU AU2018202013A patent/AU2018202013A1/en not_active Abandoned
- 2018-06-14 US US16/008,486 patent/US11612562B2/en active Active
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2019
- 2019-03-20 IL IL265501A patent/IL265501B2/en unknown
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2020
- 2020-01-21 AU AU2020200395A patent/AU2020200395B2/en active Active
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2021
- 2021-05-28 AR ARP210101446A patent/AR122198A2/es unknown
- 2021-10-07 AU AU2021245178A patent/AU2021245178B2/en active Active
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2023
- 2023-02-24 US US18/174,043 patent/US20230277442A1/en active Pending
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