AR079946A1 - Formulaciones liquidas para conjugados de accion prolongada de eritropoyetina - Google Patents

Formulaciones liquidas para conjugados de accion prolongada de eritropoyetina

Info

Publication number
AR079946A1
AR079946A1 ARP110100183A ARP110100183A AR079946A1 AR 079946 A1 AR079946 A1 AR 079946A1 AR P110100183 A ARP110100183 A AR P110100183A AR P110100183 A ARP110100183 A AR P110100183A AR 079946 A1 AR079946 A1 AR 079946A1
Authority
AR
Argentina
Prior art keywords
liquid formulation
formulation according
epo
combination
group
Prior art date
Application number
ARP110100183A
Other languages
English (en)
Inventor
Sung Min Bae
Dae Seong Im
Min Young Kim
Sung Youb Jung
Se Chang Kwon
Chang Ki Lim
Original Assignee
Hanmi Holdings Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hanmi Holdings Co Ltd filed Critical Hanmi Holdings Co Ltd
Publication of AR079946A1 publication Critical patent/AR079946A1/es

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • 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
    • A61K47/02—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • 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
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • 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
    • 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
    • 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
    • A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/6811—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a protein or peptide, e.g. transferrin or bleomycin
    • 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
    • A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
    • 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
    • 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
    • A61K9/20—Pills, tablets, discs, rods
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06—Antianaemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Dermatology (AREA)
  • Biochemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Diabetes (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Formulacion líquida que les confiere estabilidad durante períodos de tiempo prolongados a los conjugados de accion prolongada de EPO, que presentan una duracion y una estabilidad mejoradas in vivo. Comprende una composicion estabilizadora caracterizada por un amortiguador y manitol. Debido a que está libre de albumina de suero humano y de otros factores potencialmente nocivos para el cuerpo, la formulacion no presenta riesgos relacionados con las infecciones virales, al tiempo que garantiza una estabilidad excelente durante el almacenamiento de los conjugados de accion prolongada de EPO Reivindicacion 2: La formulacion líquida de acuerdo con la reivindicacion 1, caracterizada porque la concentracion del manitol varía entre 1 y 20% (p/v), sobre la base del volumen total de la formulacion líquida. Reivindicacion 6: La formulacion líquida de acuerdo con la reivindicacion 1, caracterizada porque el estabilizador libre de albumina también comprende un ingrediente seleccionado del grupo que consiste en un agente isotonico, un alcohol polihídrico, un azucar, un agente tensioactivo no ionico, un aminoácido neutro y una combinacion de éstos. Reivindicacion 7: La formulacion líquida de acuerdo con la reivindicacion 6, caracterizada porque el agente isotonico es una sal seleccionada del grupo que consiste en el cloruro de sodio, el sulfato de sodio, el citrato de sodio y una combinacion de éstas. Reivindicacion 9: La formulacion líquida de acuerdo con la reivindicacion 6, caracterizada porque el agente tensioactivo no ionico es un agente tensioactivo no ionico basado en polisorbato o basado en poloxámero. Reivindicacion 12: La formulacion líquida de acuerdo con la reivindicacion 6, caracterizada porque el azucar se selecciona del grupo que consiste en la manosa, la glucosa, la fucosa, la xilosa, la lactosa, la maltosa, la sacarosa, la rafinosa, el dextrano y una combinacion de éstos. Reivindicacion 14: La formulacion líquida de acuerdo con la reivindicacion 6, caracterizada porque el alcohol polihídrico se selecciona del grupo que consiste en el propilenglicol, el polietilenglicol de bajo peso molecular, el glicerol, el polipropileno de bajo peso molecular y una combinacion de éstos. Reivindicacion 16: La formulacion líquida de acuerdo con la reivindicacion 6, caracterizada porque el aminoácido neutro se selecciona del grupo que consiste en la glicina, la alanina, la leucina, la isoleucina y una combinacion de éstos. Reivindicacion 20: La formulacion líquida de acuerdo con la reivindicacion 1, caracterizada porque la EPO es una proteína EPO mutante modificada respecto de la EPO salvaje mediante la sustitucion, la supresion o la insercion de uno o más aminoácidos, o bien un péptido análogo con una actividad similar a la de la EPO salvaje. Reivindicacion 24: La formulacion líquida de acuerdo con la reivindicacion 22, caracterizada porque el fragmento Fc de inmunoglobulina toma la forma de un dímero o un multímero de inmunoglobulinas de cadena simple compuestas por dominios del mismo origen. Reivindicacion 27: La formulacion líquida de acuerdo con la reivindicacion 1, caracterizada porque el polímero no peptídico se selecciona del grupo que consiste en un polímero biodegradable, un polímero lipídico, la quitina, el ácido hialuronico y una combinacion de éstos.
ARP110100183A 2010-01-19 2011-01-19 Formulaciones liquidas para conjugados de accion prolongada de eritropoyetina AR079946A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR20100004840 2010-01-19

Publications (1)

Publication Number Publication Date
AR079946A1 true AR079946A1 (es) 2012-02-29

Family

ID=44307382

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP110100183A AR079946A1 (es) 2010-01-19 2011-01-19 Formulaciones liquidas para conjugados de accion prolongada de eritropoyetina

Country Status (14)

Country Link
US (1) US8829163B2 (es)
EP (1) EP2525779B1 (es)
JP (1) JP5638628B2 (es)
KR (1) KR101335765B1 (es)
CN (1) CN102753147B (es)
AR (1) AR079946A1 (es)
AU (1) AU2011207916B2 (es)
BR (1) BR112012017982A2 (es)
CA (1) CA2787652C (es)
ES (1) ES2700925T3 (es)
MX (1) MX2012008453A (es)
RU (2) RU2682720C2 (es)
TW (1) TWI417104B (es)
WO (1) WO2011090306A2 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101303388B1 (ko) * 2010-10-26 2013-09-03 한미사이언스 주식회사 지속형 인터페론 알파 결합체의 액상 제제
CA2813411C (en) 2010-11-05 2016-08-02 Rinat Neuroscience Corporation Engineered polypeptide conjugates and methods for making thereof using transglutaminase
KR20130049671A (ko) 2011-11-04 2013-05-14 한미사이언스 주식회사 생리활성 폴리펩타이드 결합체 제조 방법
AR090281A1 (es) 2012-03-08 2014-10-29 Hanmi Science Co Ltd Proceso mejorado para la preparacion de un complejo polipeptidico fisiologicamente activo
AR092862A1 (es) * 2012-07-25 2015-05-06 Hanmi Pharm Ind Co Ltd Formulacion liquida de insulina de accion prolongada y un peptido insulinotropico y metodo de preparacion
AR091902A1 (es) * 2012-07-25 2015-03-11 Hanmi Pharm Ind Co Ltd Formulacion liquida de un conjugado de insulina de accion prolongada
US10441665B2 (en) 2012-07-25 2019-10-15 Hanmi Pharm. Co., Ltd. Liquid formulation of long acting insulinotropic peptide conjugate
AR094821A1 (es) 2012-07-25 2015-09-02 Hanmi Pharm Ind Co Ltd Formulación líquida de un conjugado de péptido insulinotrópico de acción prolongada
ES2804614T3 (es) 2013-07-31 2021-02-08 Rinat Neuroscience Corp Conjugados de polipéptidos manipulados usando transglutaminasa
CA2944138C (en) * 2014-03-31 2023-06-20 Hanmi Pharm. Co., Ltd. Method for improving solubility of protein and peptide by using immunoglobulin fc fragment linkage
US11602525B2 (en) 2014-04-25 2023-03-14 Rinat Neuroscience Corp. Antibody-drug conjugates with high drug loading
CN104984323B (zh) * 2015-06-12 2018-05-01 北京四环生物制药有限公司 注射用重组人促红素冻干粉针剂
CN105311624A (zh) * 2015-11-23 2016-02-10 哈药集团生物工程有限公司 一种含有重组人促红素的药物组合物
CN106729627B (zh) * 2016-12-14 2021-07-13 深圳未名新鹏生物医药有限公司 一种重组人***制剂
WO2018142514A1 (ja) * 2017-02-01 2018-08-09 協和発酵キリン株式会社 ダルベポエチンを含む液体医薬組成物
WO2022033480A1 (zh) * 2020-08-11 2022-02-17 隆延生物科技（上海）有限公司 一种液体制剂及其应用

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TWI240627B (en) * 1996-04-26 2005-10-01 Chugai Pharmaceutical Co Ltd Erythropoietin solution preparation
PT1820516E (pt) * 1999-02-22 2013-10-31 Baxter Int Novas formulações de factor viii isentas de albumina
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BRPI0317376B8 (pt) * 2002-12-17 2021-05-25 Merck Patent Gmbh proteína de fusão de anticorpo-il2 designada como hu14.18-il2, usos da mesma, vetor e composição farmacêutica
US20050176108A1 (en) * 2003-03-13 2005-08-11 Young-Min Kim Physiologically active polypeptide conjugate having prolonged in vivo half-life
RU2268067C2 (ru) * 2003-06-09 2006-01-20 Государственное предприятие Государственный научный центр "Институт иммунологии Федерального медико-биологического агентства" (ГНЦ "Институт иммунологии ФМБА России") Вирусные вакцины
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KR100560697B1 (ko) 2003-08-06 2006-03-16 씨제이 주식회사 알부민을 함유하지 않는 에리스로포이에틴 제제
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Also Published As

Publication number Publication date
TWI417104B (zh) 2013-12-01
KR20110085918A (ko) 2011-07-27
EP2525779A4 (en) 2014-07-09
AU2011207916B2 (en) 2014-01-23
KR101335765B1 (ko) 2013-12-02
BR112012017982A2 (pt) 2016-05-03
CA2787652C (en) 2015-06-02
JP2013517325A (ja) 2013-05-16
US8829163B2 (en) 2014-09-09
RU2015103071A3 (es) 2018-09-06
EP2525779A2 (en) 2012-11-28
US20120296069A1 (en) 2012-11-22
AU2011207916A1 (en) 2012-08-23
MX2012008453A (es) 2012-11-21
EP2525779B1 (en) 2018-09-05
ES2700925T3 (es) 2019-02-20
JP5638628B2 (ja) 2014-12-10
RU2682720C2 (ru) 2019-03-21
CA2787652A1 (en) 2011-07-28
RU2012135505A (ru) 2014-02-27
CN102753147B (zh) 2017-10-31
RU2015103071A (ru) 2015-06-20
CN102753147A (zh) 2012-10-24
TW201141512A (en) 2011-12-01
WO2011090306A2 (en) 2011-07-28
WO2011090306A3 (en) 2011-12-01

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