HRP20120934T1 - Sastavi i postupci koji koriste anti-cs1 antitijela u lijeäśenju multiplog mijeloma - Google Patents

Sastavi i postupci koji koriste anti-cs1 antitijela u lijeäśenju multiplog mijeloma Download PDF

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HRP20120934T1
HRP20120934T1 HRP20120934TT HRP20120934T HRP20120934T1 HR P20120934 T1 HRP20120934 T1 HR P20120934T1 HR P20120934T T HRP20120934T T HR P20120934TT HR P20120934 T HRP20120934 T HR P20120934T HR P20120934 T1 HRP20120934 T1 HR P20120934T1
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antibody
therapeutic agents
use according
decrease
urine
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HRP20120934TT
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Daniel Afar
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Abbott Biotherapeutics Corp.
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/39558Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/475Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/57Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
    • A61K31/573Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
    • AHUMAN NECESSITIES
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    • A61K31/675Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7028Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
    • A61K31/7034Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
    • A61K31/704Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
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    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/127Liposomes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • 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
    • C07K16/22Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
    • 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
    • C07K16/2803Immunoglobulins [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
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • A61K2039/507Comprising a combination of two or more separate antibodies
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/545Medicinal preparations containing antigens or antibodies characterised by the dose, timing or administration schedule

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  • Chemical Kinetics & Catalysis (AREA)
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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (12)

1. Humanizirano anti-CS1 lgGl antitijelo i jedan ili dva terapeutska agensa za istovremenu, odvojenu ili sekvencijalnu upotrebu u liječenju multiplog mijeloma, naznačeni time da spomenuto antitijelo ima sekvencu SEQ ID NO:5 u varijabilnoj regiji teškog lanca i sekvencu SEQ ID NO:6 u varijabilnoj regiji lakog lanca, i da su jedan ili dva spomenuta terapeutska agensa deksametazon ili deksametazon i talidomid.
2. Antitijelo ijedan ili dva terapeutska agensa za upotrebu prema zahtjevu 1, naznačeni time da se spomenuto antitijelo daje intravenozno u dozama od oko 0,5mg/kg do oko 20mg/kg.
3. Antitijelo ijedan ili dva terapeutska agensa za upotrebu prema zahtjevu 1 ili zahtjevu 2, naznačeni time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju kompletan odgovor, pri čemu je kompletan odgovor definiran tako da M-protein nije otkriven u serumu ili urinu imunofiksacijom najmanje 6 tjedana i da je u koštanoj srži otkriveno manje od 5% plazma ćelija.
4. Antitijelo ijedan ili dva terapeutska agensa za upotrebu prema zahtjevu 1 ili zahtjevu 2, naznačeni time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju smanjenje M-proteina veće od 90%.
5. Antitijelo ijedan ili dva terapeutska agensa za upotrebu prema zahtjevu 1 ili zahtjevu 2, naznačeni time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju smanjenje razine seruma M-proteina veće od 50% i/ili smanjenje od 90% u izlučivanju slobodnih teških lanaca u urinu ili smanjenje do ispod 200mg/24h tijekom 6 tjedana.
6. Antitijelo ijedan ili dva terapeutska agensa za upotrebu prema zahtjevu 1 ili zahtjevu 2, naznačeni time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju smanjenje razine seruma M-proteina od 25-49% i/ili smanjenje od 50-89% u izlučivanju slobodnih teških lanaca u urinu koje i dalje prekoračuje 200mg/24h tijekom 6 tjedana.
7. Upotreba humaniziranog anti-CS1 lgGl antitijela i jednog ili dva terapeutska agensa za proizvodnju lijeka za liječenje multiplog mijeloma, naznačena time da spomenuto antitijelo u varijabilnoj regiji teškog lanca ima sekvencu SEQ ID NO:5 i u varijabilnoj regiji lakog lanca sekvencu SEQ ID NO:6, i da su spomenuti terapeutska agensi deksometazon ili deksometazon i talidomid.
8. Upotreba prema zahtjevu 7, naznačena time da se spomenuto antitijelo daje intravenozno u dozama od oko 0,5mg/kg do oko 20mg/kg.
9. Upotreba prema zahtjevu 7 ili zahtjevu 8, naznačena time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju kompletan odgovor, pri čemu je kompletan odgovor definiran time da M-protein nije otkriven u serumu ili urinu imunofiksacijom najmanje 6 tjedana i daje manje od 5% plazma ćelija otkriveno u koštanoj srži.
10. Upotreba prema zahtjevu 7 ili zahtjevu 8, naznačena time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju smanjenje M-proteina veće od 90%.
11. Upotreba prema zahtjevu 7 ili zahtjevu 8, naznačena time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju smanjenje razine M-proteina veće od 50% i/ili smanjenje od 90% u izlučivanju slobodnih lakih lanaca u urinu ili smanjenje do ispod 200mg/24h tijekom 6 tjedana.
12. Upotreba prema zahtjevu 7 ili zahtjevu 8, naznačena time da spomenuto antitijelo i jedan ili dva terapeutska agensa izazivaju smanjenje razine seruma M-proteina od 25- 49% i/ili smanjenje od 50-89% u izlučivanju slobodnih lakih lanaca u urinu koje i dalje prekoračuje 200mg/24h tijekom 6 tjedana.
HRP20120934TT 2006-08-07 2012-11-19 Sastavi i postupci koji koriste anti-cs1 antitijela u lijeäśenju multiplog mijeloma HRP20120934T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US83625006P 2006-08-07 2006-08-07
US85614406P 2006-11-01 2006-11-01
PCT/US2007/075401 WO2008019376A2 (en) 2006-08-07 2007-08-07 Compositions and methods using anti-cs1 antibodies to treat multiple myeloma

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HRP20120934T1 true HRP20120934T1 (hr) 2012-12-31

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US (3) US7842293B2 (hr)
EP (2) EP2425849A3 (hr)
JP (4) JP2010500370A (hr)
AU (1) AU2007281682B2 (hr)
BR (1) BRPI0716475A2 (hr)
CA (1) CA2660102C (hr)
CY (1) CY1113309T1 (hr)
DK (1) DK2068930T3 (hr)
ES (1) ES2391790T3 (hr)
HK (1) HK1129849A1 (hr)
HR (1) HRP20120934T1 (hr)
IL (1) IL196920A (hr)
MX (1) MX2009001440A (hr)
NO (1) NO345083B1 (hr)
NZ (1) NZ574979A (hr)
PL (1) PL2068930T3 (hr)
PT (1) PT2068930E (hr)
WO (1) WO2008019376A2 (hr)

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AU2013280644B2 (en) 2012-06-26 2018-08-02 Jeffrey A. BACHA Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or AHI1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof
JP6374392B2 (ja) 2012-11-05 2018-08-15 デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド Xbp1、cd138およびcs1ペプチド、該ペプチドを含有する薬学的組成物、ならびにかかるペプチドおよび組成物を使用する方法
JP2016519684A (ja) 2013-04-08 2016-07-07 デニス エム ブラウン 準最適に投与された薬物療法の有効性を改善するための及び/又は副作用を低減するための方法および組成物
WO2015069785A1 (en) 2013-11-06 2015-05-14 Bristol-Myers Squibb Company Combination of anti-kir and anti-cs1 antibodies to treat multiple myeloma
US20160264670A1 (en) 2013-11-06 2016-09-15 Bristol-Myers Squibb Company Immunotherapeutic dosing regimens and combinations thereof
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ES2886657T3 (es) * 2015-06-29 2021-12-20 Bristol Myers Squibb Co Regímenes de dosificación inmunoterapéutica que comprenden pomalidomida y un anticuerpo anti-CS1 para el tratamiento de cáncer
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KR20220092578A (ko) 2019-11-05 2022-07-01 브리스톨-마이어스 스큅 컴퍼니 M-단백질 검정 및 이의 용도

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EP2069478A2 (en) 2006-08-07 2009-06-17 PDL BioPharma, Inc. Use of allogeneic effector cells and anti-cs1 antibodies for selective killing of multiple myeloma cells
BRPI0716647A2 (pt) 2006-08-07 2017-05-16 Dana Farber Cancer Inst Inc processos de tratamento de mieloma múltiplo utilizando terapias de combinação baseadas em anticorpos anti-cs1
MX2009001440A (es) * 2006-08-07 2009-04-15 Pdl Biopharma Inc Composiciones y metodos que utilizan anticuerpos anti-cs1 para tratar mieloma multiple.

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WO2008019376A2 (en) 2008-02-14
JP2015157823A (ja) 2015-09-03
ES2391790T3 (es) 2012-11-29
NZ574979A (en) 2012-06-29
DK2068930T3 (da) 2012-10-29
JP2014040421A (ja) 2014-03-06
WO2008019376A3 (en) 2008-07-10
US20160206734A1 (en) 2016-07-21
BRPI0716475A2 (pt) 2016-05-03
PL2068930T3 (pl) 2013-02-28
MX2009001440A (es) 2009-04-15
HK1129849A1 (en) 2009-12-11
CA2660102C (en) 2017-02-21
JP6005205B2 (ja) 2016-10-12
EP2425849A3 (en) 2012-05-09
IL196920A (en) 2013-11-28
EP2425849A2 (en) 2012-03-07
JP2017025077A (ja) 2017-02-02
AU2007281682A1 (en) 2008-02-14
PT2068930E (pt) 2012-10-23
EP2068930B1 (en) 2012-09-19
JP5775125B2 (ja) 2015-09-09
US20080124332A1 (en) 2008-05-29
AU2007281682B2 (en) 2013-05-16
CA2660102A1 (en) 2008-02-14
JP2010500370A (ja) 2010-01-07
NO345083B1 (no) 2020-09-21
EP2068930A2 (en) 2009-06-17
US7842293B2 (en) 2010-11-30
IL196920A0 (en) 2011-08-01
NO20090969L (no) 2009-04-28
CY1113309T1 (el) 2016-04-13
US20110165154A1 (en) 2011-07-07

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