DK2493930T3 - Forbedrede anti-humane fractalkinantistoffer og anvendelser deraf. - Google Patents
Forbedrede anti-humane fractalkinantistoffer og anvendelser deraf. Download PDFInfo
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- DK2493930T3 DK2493930T3 DK10826929.1T DK10826929T DK2493930T3 DK 2493930 T3 DK2493930 T3 DK 2493930T3 DK 10826929 T DK10826929 T DK 10826929T DK 2493930 T3 DK2493930 T3 DK 2493930T3
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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
- C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
-
- 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
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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
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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
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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
- A61P1/04—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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/46—Hybrid immunoglobulins
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Claims (31)
1. Antifractalkinantistof eller fractalkinbindende fragment deraf, hvori antistoffet eller det fractalkinbindende fragment deraf omfatter en tung kæde og en let kæde, hvori den tunge kæde omfatter aminosyresekvensen ifølge SEQ ID NO: 26, og den lette kæde omfatter aminosyresekvensen ifølge NO: 27, den tunge kæde omfatter aminosyresekvensen ifølge SEQ ID NO: 36, og den lette kæde omfatter aminosyresekvensen ifølge NO: 38, den tunge kæde omfatter aminosyresekvensen ifølge SEQ ID NO: 36, og den lette kæde omfatter aminosyresekvensen ifølge NO: 44, den tunge kæde omfatter aminosyresekvensen ifølge SEQ ID NO: 37, og den lette kæde omfatter aminosyresekvensen ifølge NO: 38, den tunge kæde omfatter aminosyresekvensen ifølge SEQ ID NO: 37, og den lette kæde omfatter aminosyresekvensen ifølge NO: 44, eller den tunge kæde omfatter aminosyresekvensen ifølge SEQ ID NO: 37, og den lette kæde omfatter aminosyresekvensen ifølge NO: 45.
2. Antistof ifølge krav 1, hvori antistoffet er et intakt antistof.
3. Antistof eller fractalkinbindende fragment deraf ifølge krav 1 eller 2, hvori antistoffet eller det fractalkinbindende fragment humaniseres.
4. Antistof eller fractalkinbindende fragment deraf ifølge krav 1, 2 eller 3, hvori antistoffet eller det fractalkinbindende fragment er kimært.
5. Antistof eller fractalkinbindende fragment deraf ifølge krav 4, hvori antistoffet omfatter en tung kæde og en let kæde, hvori antistoffets variable tunge kæde-domæne omfatter aminosyresekvensen ifølge SEQ ID NO: 26, og hvori antistoffets variable lette kæde-domæne omfatte aminosyresekvensen ifølge SEQ ID NO: 27.
6. Antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-4, hvori antistoffet eller det fractalkinbindende fragment heraf omfatter en tung kæde, der omfatter aminosyresekvensen ifølge SEQ ID NO: 37, og en let kæde, der omfatter aminosyresekvensen ifølge SEQ ID NO: 44 .
7. Antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-6, der omfatter en human konstant region.
8. Antistof eller fractalkinbindende fragment deraf ifølge krav 7, der omfatter en konstant region af en IgG-isotype.
9. Antistof eller fractalkinbindende fragment deraf ifølge krav 8, der omfatter en konstant region af IgG2-isotypen.
10. Antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-9, der omfatter en muteret Fc-region således, at antistoffet har reduceret antistofafhængig cellemedieret cytotoksicitet og/eller komplementaktivering.
11. Antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af krav 1 eller kravene 3 til 9, hvori det fractalkinbindende fragment er valgt fra den gruppe, der består af et Fab, et Fab' , et F(ab')2 og et Fv, og hvori det fractalkinbindende fragment bevarer bindingsspecificiteten til fractalkin.
12. Antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-11, hvori antistoffet hæmmer bindingen mellem fractalkin og CX3CR1.
13. Antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-12 til anvendelse ved behandling af en inflammatorisk lidelse, hvori den inflammatoriske lidelse er ulcerativ colitis, Crohns sygdom eller rheumatoid arthritis.
14. Farmaceutisk sammensætning, der omfatter et antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-13.
15. Farmaceutisk sammensætning ifølge krav 14 til anvendelse ved behandling af en inflammatorisk lidelse, hvori den inflammatoriske lidelse er ulcerativ colitis, Crohns sygdom eller rheumatoid arthritis.
16. Farmaceutisk sammensætning ifølge krav 14 eller 15, hvori sammensætningen desuden omfatter en bærer.
17. Farmaceutisk sammensætning ifølge et hvilket som helst af kravene 14-16, hvori sammensætningen desuden omfatter et yderligere terapeutisk middel.
18. Nukleinsyre, der koder for et antistof eller fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-13.
19. Vektor, der omfatter nukleinsyren ifølge krav 18.
20. Vektor ifølge krav 19, hvori vektoren er en ekspressionsvektor.
21. Værtscelle, der omfatter én eller flere vektorer ifølge krav 19 eller 20.
22. Værtscelle ifølge krav 21, hvori værtscellen omfatter en første og anden vektor, idet den første vektor omfatter en nukleinsyre, der koder for en tung kæde, og den anden vektor omfatter en nukleinsyre, der koder for en let kæde af et antistof eller et fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-13.
23. Værtscelle ifølge krav 22, hvori ekspression af den tunge og lette kæde i værtscellen producerer et antistof eller et fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-13.
24. Værtscelle ifølge et hvilket som helst af kravene 21-23, hvori værtscellen er prokaryotisk.
25. Værtscelle ifølge et hvilket som helst af kravene 21-23, hvori værtscellen er eukaryotisk.
26. Værtscelle ifølge krav 25, hvori værtscellen er en pattedyrs celle.
27. Værtscelle ifølge krav 26, hvori cellen er en CHO-celle eller en NSO-celle.
28. Fremgangsmåde til fremstilling af et antifractalkinantistof eller et fractalkinbindende fragment deraf, hvilken fremgangsmåde omfatter (a) ekspression af vektoren ifølge et hvilket som helst af kravene 19 eller 20 i en egnet værtscelle og (b) udvinding af antistoffet eller det fractalkinbindende fragment deraf.
29. Fremgangsmåde ifølge krav 28, hvori antistoffet eller det fractalkinbindende fragment deraf udskilles af værtscellen i dyrkningsmedier.
30. Fremgangsmåde ifølge krav 29, hvori antistoffet eller det fractalkinbindende fragment deraf oprenses til mindst 95 % eller mere i forhold til det antistofholdige dyrkningsmedium.
31. Anvendelse af et antistof eller et fractalkinbindende fragment deraf ifølge et hvilket som helst af kravene 1-13 til fremstilling af et lægemiddel til anvendelse ved behandling af en inflammatorisk lidelse, hvorved den inflammatoriske lidelse er ulcerativ colitis, Crohns sygdom eller rheumatoid arthritis .
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25652109P | 2009-10-30 | 2009-10-30 | |
PCT/JP2010/069653 WO2011052799A1 (en) | 2009-10-30 | 2010-10-28 | Compositions and methods for treating inflammatory disorders |
Publications (1)
Publication Number | Publication Date |
---|---|
DK2493930T3 true DK2493930T3 (da) | 2018-12-17 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK10826929.1T DK2493930T3 (da) | 2009-10-30 | 2010-10-28 | Forbedrede anti-humane fractalkinantistoffer og anvendelser deraf. |
Country Status (31)
Country | Link |
---|---|
US (1) | US8932592B2 (da) |
EP (1) | EP2493930B1 (da) |
JP (2) | JP5631991B2 (da) |
KR (2) | KR102099596B1 (da) |
CN (1) | CN102597003B (da) |
AR (2) | AR078796A1 (da) |
AU (1) | AU2010312408B2 (da) |
BR (1) | BR112012010266A2 (da) |
CA (1) | CA2778895C (da) |
CL (2) | CL2012001143A1 (da) |
CY (1) | CY1121167T1 (da) |
DK (1) | DK2493930T3 (da) |
ES (1) | ES2698389T3 (da) |
HR (1) | HRP20181973T1 (da) |
HU (1) | HUE041952T2 (da) |
IL (1) | IL219470A (da) |
JO (1) | JO3437B1 (da) |
LT (1) | LT2493930T (da) |
MX (1) | MX2012005052A (da) |
MY (1) | MY158481A (da) |
NZ (1) | NZ599779A (da) |
PE (1) | PE20121645A1 (da) |
PL (1) | PL2493930T3 (da) |
PT (1) | PT2493930T (da) |
RS (1) | RS58142B1 (da) |
RU (1) | RU2569109C2 (da) |
SI (1) | SI2493930T1 (da) |
TW (1) | TWI414308B (da) |
UA (1) | UA105073C2 (da) |
WO (1) | WO2011052799A1 (da) |
ZA (1) | ZA201203002B (da) |
Families Citing this family (11)
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US9415118B2 (en) * | 2013-03-13 | 2016-08-16 | Novartis Ag | Antibody drug conjugates |
PL3221363T3 (pl) | 2014-11-21 | 2021-01-11 | Bristol-Myers Squibb Company | Przeciwciała przeciwko cd73 i ich zastosowanie |
CN113929770A (zh) | 2014-11-21 | 2022-01-14 | 百时美施贵宝公司 | 包含修饰的重链恒定区的抗体 |
EP3159007A1 (en) | 2015-10-19 | 2017-04-26 | Eisai R&D Management Co., Ltd. | Pharmaceutical composition for treating rheumatoid arthritis |
JP2017154975A (ja) * | 2016-02-29 | 2017-09-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | クローン病を治療するための医薬組成物 |
JP2018070473A (ja) * | 2016-10-26 | 2018-05-10 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 関節リウマチを治療するための医薬組成物 |
JP2018177701A (ja) * | 2017-04-14 | 2018-11-15 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | クローン病を治療するための医薬組成物 |
WO2020214166A1 (en) * | 2019-04-17 | 2020-10-22 | The Governors Of The University Of Alberta | Treatment of autoimmune liver disease |
US20220205980A1 (en) | 2019-04-23 | 2022-06-30 | Eisai R&D Management Co., Ltd. | Biomarker for rheumatoid arthritis treatment |
CN113087795A (zh) * | 2019-12-23 | 2021-07-09 | 上海普铭生物科技有限公司 | 针对趋化因子cx3cl1的抗体及其应用 |
US20230338522A1 (en) | 2020-10-30 | 2023-10-26 | Eisai R&D Management Co., Ltd. | Pharmaceutical composition |
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2010
- 2010-10-27 JO JOP/2010/0374A patent/JO3437B1/ar active
- 2010-10-28 HU HUE10826929A patent/HUE041952T2/hu unknown
- 2010-10-28 SI SI201031803T patent/SI2493930T1/sl unknown
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