AR101504A1 - Combinaciones terapéuticas de un inhibidor de la btk, un inhibidor de la pi3k, un inhibidor de la jak-2, y/o un inhibidor de la cdk4/6 - Google Patents
Combinaciones terapéuticas de un inhibidor de la btk, un inhibidor de la pi3k, un inhibidor de la jak-2, y/o un inhibidor de la cdk4/6Info
- Publication number
- AR101504A1 AR101504A1 ARP150102591A ARP150102591A AR101504A1 AR 101504 A1 AR101504 A1 AR 101504A1 AR P150102591 A ARP150102591 A AR P150102591A AR P150102591 A ARP150102591 A AR P150102591A AR 101504 A1 AR101504 A1 AR 101504A1
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- Prior art keywords
- inhibitor
- hydrates
- prodrugs
- solvates
- crystals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- 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
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicación 1: Un método de tratamiento un cáncer, que comprende la coadministración a un mamífero que lo necesita de una o más composiciones que comprenden cantidades terapéuticamente efectivas de (I) inhibidor de la quinasa 4/6 dependiente de ciclina (CDK4/6) o una de sus sales, solvatos, hidratos, cocristales o profármacos farmacéuticamente aceptables y (II) un inhibidor de la tirosina quinasa de Bruton (BTK) o una de sus sales, solvatos, hidratos, cocristales o profármacos farmacéuticamente aceptables. Reivindicación 7: El método de acuerdo con una de las reivindicaciones 1 a 6, en donde el inhibidor de BTK se selecciona del grupo que consiste en: el grupo de fórmulas (1), y sus sales, cocristales, hidratos, solvatos o profármacos farmacéuticamente aceptables. Reivindicación 8: El método de acuerdo con la reivindicación 7, que también comprende la etapa de administración de una dosis terapéuticamente efectiva de un anticuerpo anti-CD20 seleccionado del grupo que consiste en rituximab, obinutuzumab, ofatumumab, veltuzumab, tositumomab, ibritumomab y sus fragmentos, derivados, conjugados, variantes, complejos rotulados con radioisótopos y biosimilares. Reivindicación 10: El método de acuerdo con cualquiera de las reivindicaciones 1 - 9, en donde el inhibidor de CDK4/6 es palbociclib de fórmula (2), de sus sales, cocristales, hidratos, solvatos o profármacos farmacéuticamente aceptables. Reivindicación 14: El método de acuerdo con una de las reivindicaciones 2 a 13, en donde el inhibidor de PI3K se selecciona del grupo que consiste en: el grupo de fórmulas (3), y sus sales, solvatos, hidratos, cocristales o profármacos farmacéuticamente aceptables. Reivindicación 34: Una composición que comprende cantidades terapéuticamente efectivas de (I) un inhibidor de la quinasa 4/6 dependiente de ciclina (CDK4/6) o una de sus sales, solvatos, hidratos, cocristales o profármacos farmacéuticamente aceptables y (II) un inhibidor de la tirosina quinasa de Bruton (BTK) o una de sus sales, solvatos, hidratos, cocristales o profármacos farmacéuticamente aceptables, para usar en el tratamiento de cáncer. Reivindicación 49: La composición de acuerdo con la reivindicación 48, en donde el inhibidor de JAK-2 se selecciona del grupo que consiste en ruxolitinib: de fórmula (4), pacritinib: de fórmula (5), y sus sales, cocristales, hidratos, solvatos o profármacos farmacéuticamente aceptables.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462035806P | 2014-08-11 | 2014-08-11 | |
US201462088371P | 2014-12-05 | 2014-12-05 | |
US201562115512P | 2015-02-12 | 2015-02-12 | |
US201562181163P | 2015-06-17 | 2015-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR101504A1 true AR101504A1 (es) | 2016-12-21 |
Family
ID=53969402
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP150102591A AR101504A1 (es) | 2014-08-11 | 2015-08-11 | Combinaciones terapéuticas de un inhibidor de la btk, un inhibidor de la pi3k, un inhibidor de la jak-2, y/o un inhibidor de la cdk4/6 |
Country Status (4)
Country | Link |
---|---|
US (2) | US20170224819A1 (es) |
AR (1) | AR101504A1 (es) |
TW (1) | TW201618773A (es) |
WO (1) | WO2016024232A1 (es) |
Families Citing this family (17)
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LT3179991T (lt) | 2014-08-11 | 2021-11-10 | Acerta Pharma B.V. | Terapiniai btk inhibitoriaus ir bcl-2 inhibitoriaus deriniai |
EP3191098A4 (en) | 2014-09-12 | 2018-04-25 | G1 Therapeutics, Inc. | Combinations and dosing regimes to treat rb-positive tumors |
WO2017197904A2 (zh) * | 2016-05-08 | 2017-11-23 | 上海诚妙医药科技有限公司 | 帕布昔利布的新晶型及其制备方法及其用途 |
AU2017268839A1 (en) * | 2016-05-27 | 2018-11-29 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Combination of anti-CD20 antibody, P13 kinase-delta selective inhibitor, and BTK inhibitor to treat B-cell proliferative disorders |
US11395821B2 (en) | 2017-01-30 | 2022-07-26 | G1 Therapeutics, Inc. | Treatment of EGFR-driven cancer with fewer side effects |
JP2020530282A (ja) * | 2017-07-07 | 2020-10-22 | アレナ ファーマシューティカルズ, インコーポレイテッド | 組換えウリカーゼ酵素 |
PE20210121A1 (es) | 2018-01-08 | 2021-01-19 | G1 Therapeutics Inc | Regimenes de dosificacion superior de g1t38 |
US20210380710A1 (en) * | 2018-05-29 | 2021-12-09 | WuXi Biologics Ireland Limited | A novel anti-cd3/anti-cd20 bispecific antibody |
JP2021534114A (ja) * | 2018-08-14 | 2021-12-09 | エムイーアイ ファーマ,インク. | 併用療法 |
CN111377929A (zh) * | 2018-12-28 | 2020-07-07 | 南京艾德凯腾生物医药有限责任公司 | 一种可用于治疗白血病阿卡替尼(Acalabrutinib)制备的方法 |
CN113840608B (zh) * | 2019-05-30 | 2023-11-14 | 江苏恒瑞医药股份有限公司 | Cdk4/6抑制剂与vegfr抑制剂联合在制备治疗肿瘤的药物中的用途 |
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BR112015003153A2 (pt) | 2012-08-17 | 2017-07-04 | Concert Pharmaceuticals Inc | baricitinib deuterado |
MX367918B (es) | 2013-04-25 | 2019-09-11 | Beigene Ltd | Compuestos heterociclicos fusionados como inhibidores de proteina quinasa. |
US20150005277A1 (en) | 2013-06-28 | 2015-01-01 | Beigene, Ltd. | Protein Kinase Inhibitors and Uses Thereof |
AU2014339816B2 (en) * | 2013-10-25 | 2020-05-28 | Pharmacyclics Llc | Treatment using Bruton's tyrosine kinase inhibitors and immunotherapy |
US10314842B2 (en) * | 2013-12-02 | 2019-06-11 | Cornell University | Methods for treating B cell proliferative disorders |
CA2931431A1 (en) * | 2013-12-05 | 2015-06-11 | Acerta Pharma B.V. | Therapeutic combination of a pi3k inhibitor and a btk inhibitor |
WO2015193740A2 (en) * | 2014-06-17 | 2015-12-23 | Acerta Pharma B.V. | Therapeutic combinations of a btk inhibitor, a pi3k inhibitor and/or a jak-2 inhibitor |
-
2015
- 2015-08-11 TW TW104126106A patent/TW201618773A/zh unknown
- 2015-08-11 WO PCT/IB2015/056128 patent/WO2016024232A1/en active Application Filing
- 2015-08-11 US US15/503,224 patent/US20170224819A1/en not_active Abandoned
- 2015-08-11 AR ARP150102591A patent/AR101504A1/es unknown
-
2018
- 2018-05-17 US US15/982,569 patent/US20180250400A1/en not_active Abandoned
Also Published As
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US20170224819A1 (en) | 2017-08-10 |
US20180250400A1 (en) | 2018-09-06 |
WO2016024232A1 (en) | 2016-02-18 |
TW201618773A (zh) | 2016-06-01 |
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