DK2760471T3 - Terapeutiske peptider - Google Patents

Terapeutiske peptider Download PDF

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DK2760471T3
DK2760471T3 DK12835118.6T DK12835118T DK2760471T3 DK 2760471 T3 DK2760471 T3 DK 2760471T3 DK 12835118 T DK12835118 T DK 12835118T DK 2760471 T3 DK2760471 T3 DK 2760471T3
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antibody
seq
ser
artificial sequence
gly
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Kai W Wucherpfennig
Kenneth May Jr
Glenn Dranoff
F Stephen Hodi
Christopher Harvey
Bettina Franz
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Dana Farber Cancer Inst Inc
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    • 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
    • C07K16/2803Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2833Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against MHC-molecules, e.g. HLA-molecules
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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    • A61K49/14Peptides, e.g. proteins
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    • A61K31/365Lactones
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    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565Complementarity determining region [CDR]
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    • C07K2317/00Immunoglobulins specific features
    • C07K2317/90Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/92Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value

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Claims (14)

  1. TERAPEUTISKE PEPTIDER
    1. Sammensætning omfattende et antistof eller antistoffragment, der immunspecifikt binder til MHC klasse I polypeptid-relateret sekvens A (MICA), hvor antistoffet eller antistoffragmentet omfatter en variabel tungkæderegion (VH) og en variabel letkæderegion (VL) og, (a) komplementaritetsbestemmende region (CDR) 3 ifølge SEQ ID NO: 212 af VH af antistof ID 9; eller (b) komplementaritetsbestemmende region (CDR) 3 ifølge SEQ ID NO: 158 af VH af antistof ID 6.
  2. 2. Sammensætning ifølge krav 1, hvor antistoffet eller antistoffragmentet omfatter, (a) komplementaritetsbestemmende region (CDR) 3 ifølge SEQ ID NO: 212 af VH af antistof ID 9, og CDR3 ifølge SEQ ID NO: 219 af VL af antistoflD 9; eller (b) komplementaritetsbestemmende region (CDR) 3 ifølge SEQ ID NO: 158 af VH af antistof ID 6, og CDR3 ifølge SEQ ID NO: 164 af VL af antistof ID 6.
  3. 3. Sammensætning ifølge krav 1 eller krav 2, hvor antistoffet eller antistoffragmentet ifølge (a) endvidere omfatter komplementaritetsbestemmende region CDR2 ifølge SEQ ID NO: 210 af VH af antistof ID 9, og CDR2 ifølge SEQ ID NO: 217 af VL af antistof ID 9; eller hvor peptidet ifølge (b) endvidere omfatter komplementaritetsbestemmende region CDR2 ifølge SEQ ID NO: 156 af Vh af antistof ID 6, og CDR2 ifølge SEQ ID NO: 162 af VL af antistoflD 6.
  4. 4. Sammensætning ifølge et hvilket som helst af kravene 1-3, hvor antistoffet eller antistofifragmentet ifølge (a) omfatter komplementaritetsbestemmende region CDR1 ifølge SEQ ID NO: 208 af VH af antistof ID 9, og CDR1 ifølge SEQ ID NO: 215 af VL af antistof ID 9; eller hvor peptidet ifølge (b) omfatter komplementaritetsbestemmende region CDR1 ifølge SEQ ID NO: 153 afVH af antistoflD 6, og CDR1 ifølge SEQ ID NO: 160 af VL af antistoflD 6.
  5. 5. Sammensætning ifølge et hvilket som helst af kravene 1-4, hvor antistoffet eller antistoffragmentet omfatter: (a) en VH-kæde med mindst 95 %, 96 %, 97 %, 98 eller 99 % identitet med SEQ ID NO: 204; eller (b) en VH-kæde med mindst 95 %, 96 %, 97 %, 98 eller 99 % identitet med SEQ ID NO: 149.
  6. 6. Sammensætning ifølge et hvilket som helst af kravene 1-5, hvor antistoffet eller antistoffragmentet omfatter (a) en VL-kæde med mindst 95 %, 96 %, 97 %, 98 eller 99 % identitet med aminosyresekvensen ifølge SEQ ID NO: 206, hvor VL ikke omfatter mere end én aminosyresubstitution inde i CDR’eme i forhold til VL-CDR1-aminosyresekvensen ifølge SEQ ID NO: 215, VL, CDR2-aminosyresekvensen ifølge SEQ ID NO: 217 og VL-CDR3-aminosyresekvensen ifølge SEQ ID NO: 219; eller (b) en VL-kæde med mindst 95 %, 96 %, 97 %, 98 eller 99 % identitet med aminosyresekvensen ifølge SEQ ID NO: 151, hvor VL ikke omfatter mere end én aminosyresubstitution inde i CDR’eme i forhold til VL-CDRl-aminosyresekvensen ifølge SEQ ID NO: 160, VL-CDR2-aminosyresekvensen ifølge SEQ ID NO: 162 og VL-CDR3-aminosyresekvensen ifølge SEQ ID NO: 164.
  7. 7. Sammensætning ifølge et hvilket som helst af kravene 1-6, hvor antistoffet eller antistoffragmentet omfatter (a) en VH-CDR1, der omfatter aminosyresekvensen ifølge SEQ ID NO: 208, en VH-CDR2, der omfatter aminosyresekvensen ifølge SEQ ID NO: 210, en VH-CDR3, der omfatter aminosyresekvensen ifølge SEQ ID NO: 212, en VL-CDR1, der omfatter aminosyresekvensen ifølge SEQ ID NO: 215, en VL-CDR2, der omfatter aminosyresekvensen ifølge SEQ ID NO: 217 og en VL-CDR3, der omfatter aminosyresekvensen ifølge SEQ ID NO: 219; eller (b) en Vh-CDR1, der omfatter aminosyresekvensen ifølge SEQ ID NO: 153, en VH-CDR2, der omfatter aminosyresekvensen ifølge SEQ ID NO: 156, en VH-CDR3, der omfatter aminosyresekvensen ifølge SEQ ID NO: 158, en Vl-CDR1, der omfatter aminosyresekvensen ifølge SEQ ID NO: 160, en VL-CDR2, der omfatter aminosyresekvensen ifølge SEQ ID NO: 162 og en VL-CDR3, der omfatter aminosyresekvensen ifølge SEQ ID NO: 164.
  8. 8. Sammensætning ifølge krav 7, hvor antistoffet eller antistoffragmentet omfatter (a) en VH med mindst 95 %, 96 %, 97 %, 98 % eller 99 % identitet med aminosyresekvensen ifølge SEQ ID NO: 204 og en VL-kæde med mindst 95 %, 96 %, 97 %, 98 % eller 99 % identitet med aminosyresekvensen ifølge SEQ ID NO: 206; eller VH-kæde med mindst 95 %, 96 %, 97 %, 98 % eller 99 % identitet med aminosyresekvensen ifølge SEQ ID NO: 149 og en VT,-kæde med mindst 95 %, 96 %, 97 %, 98 % eller 99 % identitet med aminosyresekvensen ifølge SEQ ID NO: 151.
  9. 9. Sammensætning ifølge krav 8, hvor antistoffet eller antistoffragmentet omfatter en VH-kæde, der omfatter SEQ ID NO: 204 og en VL-kæde, der omfatter SEQ ID NO: 206; eller en VH-kæde, der omfatter SEQ ID NO: 149 og en VL-kæde, der omfatter SEQ ID NO: 151.
  10. 10. Sammensætning ifølge et hvilket som helst af kravene 1-9, hvilken sammensætning endvidere omfatter et anticancermiddel.
  11. 11. Sammensætning ifølge et hvilket som helst af kravene 1-10 formuleret som en farmaceutisk sammensætning.
  12. 12. Sammensætning ifølge et hvilket som helst af kravene 1-11, hvilken sammensætning endvidere omfatter en histondeacetylasehæmmer (HDAC) udvalgt fra gruppen bestående af hydroxamsyre, vorinostat, suberoylanilid-hydiOxamsyre (SAHA, trichostatin A (TSA), LAQ824, panobinostat (LBH589), belinostat (PXD101), ITF2357 italfarmaco SpA, cyklisk tetrapeptid, depsipeptid (romidepsin, FK228), benzamid; entinostat (SNDX-275/MS-275), MGCD0103, kortkædede alifatiske syrer, valproinsyre, phenylbutyrat, AN-9, pivanex, CHR-3996 og CHR-2845.
  13. 13. Sammensætning ifølge et hvilket som helst af kravene 1-12, hvilken sammensætning endvidere omfatter en proteasom-hæmmer udvalgt fra gruppen bestående af bortezomib, NPI-0052, carfilzomib (PR-171), CEP 18770, ogMLN9708.
  14. 14. Sammensætning ifølge et hvilket som helst af kravene 1-13, hvilken sammensætning endvidere omfatter et antistof udvalgt fra gruppen bestående af et anti-CTLA-4-antistof, et anti-PD-1 antistof, et anti-PDL-1 antistof og en kombination af ét eller flere deraf.
DK12835118.6T 2011-09-30 2012-09-28 Terapeutiske peptider DK2760471T3 (da)

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