DK2516468T3 - Anti-flt3-antistoffer og fremgangsmåder til anvendelse af disse - Google Patents

Anti-flt3-antistoffer og fremgangsmåder til anvendelse af disse Download PDF

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DK2516468T3
DK2516468T3 DK10798340.5T DK10798340T DK2516468T3 DK 2516468 T3 DK2516468 T3 DK 2516468T3 DK 10798340 T DK10798340 T DK 10798340T DK 2516468 T3 DK2516468 T3 DK 2516468T3
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antibody
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antibodies
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val
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DK10798340.5T
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Hans-Jörg Bühring
Martin Hofmann
Steffen Aulwurm
Ludger Grosse-Hovest
Grundram Jung
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Synimmune Gmbh
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2896Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against molecules with a "CD"-designation, not provided for elsewhere
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/72Increased effector function due to an Fc-modification
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/732Antibody-dependent cellular cytotoxicity [ADCC]

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Immunology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (15)

  1. ANTI-FLT3-ANTIST0FFER OG FREMGANGSMÅDER TIL ANVENDELSE AF DISSE
    1. IgG-antistof, der binder human receptortyrosinkinase FLT3, hvilket antistof omfatter en tung kæde og en let kæde og en aminosyresubstitution i den konstante region i forhold til et moder-anti-FLT3-antistof, hvor aminosyresubstitutionen omfatter aminosyresubstitutionerne S239D og I332E, hvor positionsnummereringen er ifølge EU-indekset.
  2. 2. Antistof ifølge krav 1, hvor Vl-CDR1 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 1; Vl-CDR2 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 2; Vl-CDR3 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 3; Vh-CDR1 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 4; Vh-CDR2 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 5; og VH-CDR3 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 6.
  3. 3. Antistof ifølge krav 1, hvor Vl-CDR1 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 7; Vl-CDR2 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 8; Vl-CDR3 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 9; Vr-CDRI omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 10; VH-CDR2 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 11; og VH-CDR3 omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 12.
  4. 4. Antistof ifølge krav 2, hvor den tunge kæde omfatter et Vn-domæne, der omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 14, og den lette kæde omfatter et VL-domæne, der omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 13.
  5. 5. Antistof ifølge krav 3, hvor den tunge kæde omfatter et VH-domæne, der omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 30, og den lette kæde omfatter et VL-domæne, der omfatter eller består af aminosyresekvensen, der er vist i SEQ ID NO: 29.
  6. 6. Antistof ifølge krav 1, hvor antistoffet er et kimerisk antistof og omfatter en tung kæde med aminosyresekvensen, der er vist i SEQ ID NO: 27, og en let kæde med aminosyresekvensen, der er vist i SEQ ID NO: 23.
  7. 7. Antistof ifølge krav 1, hvor antistoffet er et kimerisk antistof og omfatter en tung kæde med amino syre sekvens en, der er vist i SEQ ID NO: 43, og/eller en let kæde med aminosyresekvensen, der er vist i SEQ ID NO: 39.
  8. 8. Antistof ifølge et hvilket som helst af kravene 1-7, hvor antistoffet binder med forøget affinitet til FcyRIIIa-receptoren eller har forøget ADCC-effektorfunktion sammenlignet med moderantistoffet.
  9. 9. Nukleinsyremolekyle, der koder for en tung og let kæde af antistoffet ifølge et hvilket som helst af kravene 1-8.
  10. 10. Antistof ifølge et hvilket som helst af kravene 1-8 til anvendelse i en fremgangsmåde til behandling af et lymfom eller en leukæmi hos et pattedyr.
  11. 11. Antistof til anvendelse ifølge krav 10, hvor lymfomet eller leukæmien er i stadiet minimal restsygdom (MRD).
  12. 12. Antistof til anvendelse ifølge krav 10 eller 11, hvor lymfomet eller leukæmien er udvalgt fra gruppen, der består af: non-Hodgkins lymfomer (NHL), kronisk lymfocytisk leukæmi (CLL), B-celle akut lymfoblastær leukæmi/lymfom (B-ALL), mantle celle lymfom (MCL), hårcelleleukæmi (HCL), kronisk myeloid leukæmi (CML), akut myeloid leukæmi (AML) og multipelt myelom (MM).
  13. 13. Antistof til anvendelse ifølge et hvilket som helst af kravene 10-12, hvor antistoffet administreres i kombination med mindst ét middel, der er udvalgt fra gruppen, der består af et cytotoksisk middel, et kemoterapeutisk middel, et cytokin, et væksthæmmende middel, et antihormonelt middel, en kinasehæmmer, et antiangiogent middel, et hjertebeskyttende middel, et immunstimulatorisk middel, et immunsuppressivt middel, en angiogenesehæmmer, en proteintyrosinkinasehæmmer og et andet antistof.
  14. 14. Farmaceutisk sammensætning, der omfatter antistoffet ifølge et hvilket som helst af kravene 1-8 og et farmaceutisk acceptabelt bæremateriale.
  15. 15. Transficeret cellelinje, der danner et antistof ifølge et hvilket som helst af kravene 1-8.
DK10798340.5T 2009-12-23 2010-12-23 Anti-flt3-antistoffer og fremgangsmåder til anvendelse af disse DK2516468T3 (da)

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US28952909P 2009-12-23 2009-12-23
PCT/EP2010/070659 WO2011076922A1 (en) 2009-12-23 2010-12-23 Anti-flt3 antibodies and methods of using the same

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EP (1) EP2516468B1 (da)
JP (1) JP5944831B2 (da)
CN (1) CN102770453B (da)
BR (1) BR112012015740B1 (da)
CA (1) CA2785178C (da)
DK (1) DK2516468T3 (da)
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HK (1) HK1172910A1 (da)
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US20120328612A1 (en) 2012-12-27
EP2516468A1 (en) 2012-10-31
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JP5944831B2 (ja) 2016-07-05
HRP20160422T1 (hr) 2016-05-20
EA027502B1 (ru) 2017-08-31
CN102770453A (zh) 2012-11-07
CA2785178A1 (en) 2011-06-30
WO2011076922A1 (en) 2011-06-30
HUE028629T2 (en) 2016-12-28
JP2013515472A (ja) 2013-05-09
CN102770453B (zh) 2014-10-08
CA2785178C (en) 2019-09-03
EP2516468B1 (en) 2016-03-02
US9023996B2 (en) 2015-05-05
EA201290370A1 (ru) 2013-04-30
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SI2516468T1 (sl) 2016-06-30
BR112012015740A2 (pt) 2017-04-25

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