DK2155248T3 - Målretning mod abcb5 til cancerterapi - Google Patents

Målretning mod abcb5 til cancerterapi Download PDF

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DK2155248T3
DK2155248T3 DK08742787.8T DK08742787T DK2155248T3 DK 2155248 T3 DK2155248 T3 DK 2155248T3 DK 08742787 T DK08742787 T DK 08742787T DK 2155248 T3 DK2155248 T3 DK 2155248T3
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abcb5
antibody
cells
seq
melanoma
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DK08742787.8T
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Markus H Frank
Natasha Y Frank
Mohamed H Sayegh
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Brigham & Womens Hospital
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • 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
    • A61K47/6851—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 the antibody targeting a determinant of a tumour cell
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/713—Double-stranded nucleic acids or oligonucleotides
    • 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
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46—Hydrolases (3)
    • A61K38/47—Hydrolases (3) acting on glycosyl compounds (3.2), e.g. cellulases, lactases
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
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    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1135—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against oncogenes or tumor suppressor genes
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    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/575—Immunoassay; Biospecific binding assay; Materials therefor for cancer
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    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/575—Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/5758—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumours, cancers or neoplasias, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides or metabolites
    • G01N33/5759—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumours, cancers or neoplasias, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides or metabolites involving compounds localised on the membrane of tumour or cancer cells
    • 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
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    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565—Complementarity determining region [CDR]
    • 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
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]
    • 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
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/734—Complement-dependent cytotoxicity [CDC]
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    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/10—Type of nucleic acid
    • C12N2310/14—Type of nucleic acid interfering nucleic acids [NA]
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    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/30—Chemical structure
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    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/02—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2) hydrolysing N-glycosyl compounds (3.2.2)
    • C12Y302/02022—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2) hydrolysing N-glycosyl compounds (3.2.2) rRNA N-glycosylase (3.2.2.22)
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    • G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants

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Claims (7)

1. Sammensætning til anvendelse til behandling af en person med melanom, hvilken sammensætning omfatter et anti-ABCB5-antistof eller et antigenbindende fragment deraf, der har mindst ét humant område, hvilket anti-ABCB5-antistof eller antigenbindende fragment deraf omfatter 1) et variabelt immunoglobulin-domæne af tung kæde, hvor: (i) CDR1-H1 omfatter en aminosyresekvens ifølge SEQ ID NO: 3; (ii) CDR2-H2 omfatter en aminosyresekvens ifølge SEQ ID NO: 4; og (i i i) CDR3-H3-sekvensen omfatter en aminosyresekvens ifølge SEQ ID NO: 5, og yderligere omfatter 2) et variabelt immunoglobulin-domæne af let kæde, hvor: (i) CDR1-L1 omfatter en aminosyresekvens ifølge SEQ ID NO: 6; (ii) CDR2-L2 omfatter en aminosyresekvens ifølge SEQ ID NO: 7; og (i i i) CDR3-L3-sekvensen omfatter en aminosyresekvens ifølge SEQ ID NO: 8.
2. Anvendelse af en sammensætning til fremstilling af et medikament til behandling af en person med melanom, hvilken sammensætning omfatter et anti-ABCB5-antistof eller et antigenbindende fragment deraf, der har mindst ét humant område, hvilket anti-ABCB5-antistof eller antigenbindende fragment deraf omfatter 1) et variabelt immunoglobulin-domæne af tung kæde, hvor: (i) CDR1-H1 omfatter en aminosyresekvens ifølge SEQ ID NO: 3; (ii) CDR2-H2 omfatter en aminosyresekvens ifølge SEQ ID NO: 4; og (i i i) CDR3-H3-sekvensen omfatter en aminosyresekvens ifølge SEQ ID NO: 5, og yderligere omfatter 2) et variabelt immunoglobulin-domæne af let kæde, hvor: (i) CDR1-L1 omfatter en aminosyresekvens ifølge SEQ ID NO: 6; (ii) CDR2-L2 omfatter en aminosyresekvens ifølge SEQ ID NO: 7; og (iii) CDR3-L3-sekvensen omfatter en aminosyresekvens ifølge SEQ ID NO: 8 .
3. Sammensætning ifølge krav 1 eller anvendelse ifølge krav 2, hvor antistoffet er en enkeltkædet Fv, et monoklonalt antistof, et bispecifikt antistof eller et syntetisk antistof.
4. Sammensætning ifølge krav 1 eller anvendelse ifølge krav 2, der omfatter mindst to variable antistofdomæner, der omfatter: (a) det variable antistofdomæne af tung kæde ifølge SEQ ID NO: 1; og (b) det variable antistof domæne af let kæde ifølge SEQ ID NO: 2.
5. Sammensætning ifølge krav 1 eller anvendelse ifølge krav 2, hvor antistoffet er et fuldstændigt humant isoleret antistof.
6. Sammensætning ifølge krav 1 eller anvendelse ifølge krav 2, der yderligere omfatter et dimeriseringsdomæne, der er koblet til det C-terminale område af et variabelt domæne af tung kæde-polypeptid.
7. Sammensætning ifølge krav 1 eller anvendelse ifølge krav 2, hvor anti-ABCB5-antistoffet eller det antigenbindende fragment deraf er et kimært antistof, der omfatter et variabelt domæne, der binder specifikt til ABCB5, og et konstant domæne, hvor det variable domæne og det konstante domæne er fra forskellige arter.
DK08742787.8T 2007-04-12 2008-04-11 Målretning mod abcb5 til cancerterapi DK2155248T3 (da)

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US92312807P 2007-04-12 2007-04-12
US705907P 2007-12-11 2007-12-11
PCT/US2008/004715 WO2008127656A1 (en) 2007-04-12 2008-04-11 Targeting abcb5 for cancer therapy

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DK2155248T3 true DK2155248T3 (da) 2015-09-14

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DK13163810.8T DK2644205T3 (da) 2007-04-12 2008-04-11 Målretning af ABCB5 til cancerterapi

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US (4) US7928202B2 (da)
EP (3) EP3431103B1 (da)
JP (4) JP5889527B2 (da)
AU (1) AU2008239633B2 (da)
CA (1) CA2718573C (da)
CY (2) CY1116823T1 (da)
DK (2) DK2155248T3 (da)
ES (2) ES2547016T3 (da)
HR (2) HRP20150934T1 (da)
HU (2) HUE039385T2 (da)
LT (1) LT2644205T (da)
PL (2) PL2644205T3 (da)
PT (2) PT2644205T (da)
SI (2) SI2155248T1 (da)
WO (1) WO2008127656A1 (da)

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