MX358013B - Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3. - Google Patents

Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3.

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Publication number
MX358013B
MX358013B MX2016008205A MX2016008205A MX358013B MX 358013 B MX358013 B MX 358013B MX 2016008205 A MX2016008205 A MX 2016008205A MX 2016008205 A MX2016008205 A MX 2016008205A MX 358013 B MX358013 B MX 358013B
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MX
Mexico
Prior art keywords
methods
treating
preventing
agent
associated diseases
Prior art date
Application number
MX2016008205A
Other languages
English (en)
Inventor
Hettmann Thore
j freeman Daniel
Radinsky Robert
Original Assignee
Amgen Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Amgen Inc filed Critical Amgen Inc
Publication of MX358013B publication Critical patent/MX358013B/es

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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/40Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
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    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19Cytokines; Lymphokines; Interferons
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    • 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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    • A61K47/50Medicinal 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
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    • A61K47/68Medicinal 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
    • A61K47/6835Medicinal 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
    • A61K47/6871Medicinal 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 an enzyme
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/10X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
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    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475Growth factors; Growth regulators
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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
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    • C07KPEPTIDES
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    • C07K16/22Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
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    • C07ORGANIC CHEMISTRY
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    • C07K16/24Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
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    • C07K16/28Immunoglobulins [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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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
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    • C07K16/32Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against translation products of oncogenes
    • AHUMAN NECESSITIES
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    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
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    • 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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    • C07K2317/622Single chain antibody (scFv)
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    • C07K2317/626Diabody or triabody
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    • C07K2317/92Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value

Abstract

La presente invención se refiere a el uso de una composición farmacéutica que comprende un primer agente y un segundo agente, para preparar un medicamento para tratar o provenir un cáncer de pulmón asociado con HER-3, en donde el primer agente es una proteína de unión al antígeno que se une a HER-3 que comprende: una secuencia de aminoácidos de cadena pesada que comprende un CDRH1 que tiene una secuencia SEQ ID NO: 256, UN CDRH2 que tiene una secuencia SEQ LID NO: 282 y , un CDRH3 que tiene una secuencia SEQ ID NO: 315 y una secuencia de aminoácidos de cadena ligera que comprende un CDRL1 que tiene una secuencia SEQ ID NO: 340, un CDRL2 que tiene una secuencia SEQ ID NO: 344 y, un CDRL3 que tiene una secuencia SEQ ID NO: 387 y; el segundo agente es lapatinib.
MX2016008205A 2009-11-13 2010-11-12 Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3. MX358013B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US26114909P 2009-11-13 2009-11-13
PCT/US2010/056430 WO2011060206A2 (en) 2009-11-13 2010-11-12 Material and methods for treating or preventing her-3 associated diseases

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MX358013B true MX358013B (es) 2018-08-01

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MX2016002120A MX357972B (es) 2009-11-13 2010-11-12 Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3.
MX2012005589A MX349513B (es) 2009-11-13 2010-11-12 Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3.
MX2016008205A MX358013B (es) 2009-11-13 2010-11-12 Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3.

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MX2012005589A MX349513B (es) 2009-11-13 2010-11-12 Materiales y metodos para el tratamiento o prevencion de enfermedades asociadas al her-3.

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EP (5) EP3670539A1 (es)
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AR (1) AR080564A1 (es)
AU (1) AU2010319483B2 (es)
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