MX2022013757A - Metodos para el tratamiento del cancer con una combinacion de un antagonista de la pd-1, una quimioterapia con terapia de radiacion, y un inhibidor de parp. - Google Patents

Metodos para el tratamiento del cancer con una combinacion de un antagonista de la pd-1, una quimioterapia con terapia de radiacion, y un inhibidor de parp.

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Publication number
MX2022013757A
MX2022013757A MX2022013757A MX2022013757A MX2022013757A MX 2022013757 A MX2022013757 A MX 2022013757A MX 2022013757 A MX2022013757 A MX 2022013757A MX 2022013757 A MX2022013757 A MX 2022013757A MX 2022013757 A MX2022013757 A MX 2022013757A
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Mexico
Prior art keywords
combination
treating cancer
antagonist
methods
parp inhibitor
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Application number
MX2022013757A
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English (en)
Inventor
Roger M Perlmutter
Maria Catherine Pietanza
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Merck Sharp & Dohme Llc
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Application filed by Merck Sharp & Dohme Llc filed Critical Merck Sharp & Dohme Llc
Publication of MX2022013757A publication Critical patent/MX2022013757A/es

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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
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    • 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
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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    • A61K31/365Lactones
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    • 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
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    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
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    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • A61K31/7048Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
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    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
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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
    • C07K16/2803Immunoglobulins [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
    • C07K16/2818Immunoglobulins [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 CD28 or CD152
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    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/10X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
    • A61N2005/1092Details
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    • C07K2317/76Antagonist effect on antigen, e.g. neutralization or inhibition of binding

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  • Health & Medical Sciences (AREA)
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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Se proporcionan en el presente documento métodos para el tratamiento del cáncer a través del uso de una combinación de (a) uno o más antagonistas de la proteína de muerte programada 1 (PD-1, por sus siglas en inglés), (b) una terapia de radiación, (c) uno o más inhibidores de la poli (ADP-ribosa) polimerasa (PARP) y, de un modo opcional, (d) una o más quimioterapias. También se proporciona en el presente documento un kit para una administración farmacéutica que comprende: (a) un antagonista de la PD-1; (b) una terapia de radiación; (c) un inhibidor de la PARP; y (d) de un modo opcional, una quimioterapia. Además, se proporcionan en el presente documento los usos de una combinación para el tratamiento del cáncer en un paciente humano, en donde la combinación comprende: (a) una cantidad eficaz de uno o más antagonistas de la PD-1, (b) una cantidad eficaz de una terapia de radiación, (c) una cantidad eficaz de un inhibidor de la PARP, y (d) de un modo opcional, una o más quimioterapias.
MX2022013757A 2020-05-04 2021-04-29 Metodos para el tratamiento del cancer con una combinacion de un antagonista de la pd-1, una quimioterapia con terapia de radiacion, y un inhibidor de parp. MX2022013757A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202063019699P 2020-05-04 2020-05-04
PCT/US2021/029777 WO2021225851A1 (en) 2020-05-04 2021-04-29 Methods of treating cancer using a combination of a pd-1 antagonist, a chemoradiation therapy and a parp inhibitor

Publications (1)

Publication Number Publication Date
MX2022013757A true MX2022013757A (es) 2022-11-30

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MX2022013757A MX2022013757A (es) 2020-05-04 2021-04-29 Metodos para el tratamiento del cancer con una combinacion de un antagonista de la pd-1, una quimioterapia con terapia de radiacion, y un inhibidor de parp.

Country Status (10)

Country Link
US (1) US20230338521A1 (es)
EP (1) EP4146275A4 (es)
JP (1) JP2023524270A (es)
KR (1) KR20230006888A (es)
CN (1) CN115996726A (es)
AU (1) AU2021268579A1 (es)
BR (1) BR112022022304A2 (es)
CA (1) CA3177576A1 (es)
MX (1) MX2022013757A (es)
WO (1) WO2021225851A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112023023833A2 (pt) * 2021-05-24 2024-01-30 Astrazeneca Ab Composições e métodos para tratamento de câncer de pulmão

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2558866B1 (en) * 2010-04-15 2016-08-17 Tracon Pharmaceuticals, Inc. Potentiation of anti-cancer activity through combination therapy with ber pathway inhibitors
US20190381127A1 (en) * 2016-02-02 2019-12-19 Splash Pharmaceuticals, Inc. Combination therapy with a6, chemotherapeutic agents, radiation therapy, or a combination thereof for the treatment of cancer
WO2019075032A1 (en) * 2017-10-13 2019-04-18 Merck Patent Gmbh COMBINATION OF A PARP INHIBITOR AND A PD-1 AXIS BINDING ANTAGONIST

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Publication number Publication date
KR20230006888A (ko) 2023-01-11
EP4146275A4 (en) 2024-05-29
WO2021225851A1 (en) 2021-11-11
CA3177576A1 (en) 2021-11-11
US20230338521A1 (en) 2023-10-26
JP2023524270A (ja) 2023-06-09
BR112022022304A2 (pt) 2022-12-20
CN115996726A (zh) 2023-04-21
EP4146275A1 (en) 2023-03-15
AU2021268579A1 (en) 2022-12-01

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