MX2021005011A - Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7). - Google Patents
Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7).Info
- Publication number
- MX2021005011A MX2021005011A MX2021005011A MX2021005011A MX2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A
- Authority
- MX
- Mexico
- Prior art keywords
- methods
- cdk7
- biomarkers
- cyclin
- identified
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 239000000090 biomarker Substances 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 238000011282 treatment Methods 0.000 title abstract 2
- 102100026810 Cyclin-dependent kinase 7 Human genes 0.000 title 2
- 101710106276 Cyclin-dependent kinase 7 Proteins 0.000 title 2
- 239000003112 inhibitor Substances 0.000 title 1
- 239000003814 drug Substances 0.000 abstract 2
- 229940124597 therapeutic agent Drugs 0.000 abstract 2
- 229940125888 CDK7 inhibitor Drugs 0.000 abstract 1
- 238000011319 anticancer therapy Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- OBJNFLYHUXWUPF-IZZDOVSWSA-N n-[3-[[5-chloro-4-(1h-indol-3-yl)pyrimidin-2-yl]amino]phenyl]-4-[[(e)-4-(dimethylamino)but-2-enoyl]amino]benzamide Chemical compound C1=CC(NC(=O)/C=C/CN(C)C)=CC=C1C(=O)NC1=CC=CC(NC=2N=C(C(Cl)=CN=2)C=2C3=CC=CC=C3NC=2)=C1 OBJNFLYHUXWUPF-IZZDOVSWSA-N 0.000 abstract 1
- 230000037361 pathway Effects 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
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- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
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- 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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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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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- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
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- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
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- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
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- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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- C07—ORGANIC CHEMISTRY
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Abstract
La presente invención se refiere a métodos para identificar pacientes que padezcan varios tipos de cáncer que tengan más probabilidades de responder al tratamiento con un inhibidor de CDK7 conforme a la Fórmula estructural (I), (Ia), una especie del mismo o una forma específica del mismo (tal como descrito en el presente documento), ya sea cuando se administre o se use solo o en combinación con un segundo agente terapéutico (por ejemplo, otra terapia contra el cáncer). Los pacientes se identifican en función de una o más características (por ejemplo, número de copias de genes o nivel de expresión) de ciertos biomarcadores (por ejemplo, RB1 u otro miembro de la vía de E2F). Además, la presente invención se refiere a métodos para tratar a un paciente identificado con un compuesto que se ajusta a la Fórmula estructural (I), (Ia), una especie del mismo o una forma específica del mismo, ya sea solo o en combinación con un segundo agente terapéutico. En otro aspecto, la presente invención presenta kits que incluyen instrucciones para tratar a un paciente identificado como se describe en el presente documento.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862754398P | 2018-11-01 | 2018-11-01 | |
US201962877189P | 2019-07-22 | 2019-07-22 | |
US201962915983P | 2019-10-16 | 2019-10-16 | |
US201962927469P | 2019-10-29 | 2019-10-29 | |
PCT/US2019/059535 WO2020093006A1 (en) | 2018-11-01 | 2019-11-01 | Methods of treating cancer in biomarker-identified patients with non-covalent inhibitors of cyclin-dependent kinase 7 (cdk7) |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2021005011A true MX2021005011A (es) | 2021-07-21 |
Family
ID=70464735
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2021005011A MX2021005011A (es) | 2018-11-01 | 2019-11-01 | Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7). |
MX2021005007A MX2021005007A (es) | 2018-11-01 | 2019-11-01 | Inhibidores de cinasa 7 dependiente de ciclina (cdk7). |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2021005007A MX2021005007A (es) | 2018-11-01 | 2019-11-01 | Inhibidores de cinasa 7 dependiente de ciclina (cdk7). |
Country Status (16)
Country | Link |
---|---|
US (3) | US12240869B2 (es) |
EP (2) | EP3873462A4 (es) |
JP (2) | JP2022508055A (es) |
KR (1) | KR20210118812A (es) |
CN (2) | CN113677346A (es) |
AU (2) | AU2019371454A1 (es) |
BR (1) | BR112021008516A2 (es) |
CA (2) | CA3118330A1 (es) |
CO (1) | CO2021007230A2 (es) |
CR (1) | CR20210287A (es) |
IL (1) | IL282737B1 (es) |
MX (2) | MX2021005011A (es) |
PH (1) | PH12021550995A1 (es) |
SG (1) | SG11202104438VA (es) |
WO (2) | WO2020093006A1 (es) |
ZA (1) | ZA202102999B (es) |
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RU2019103870A (ru) * | 2016-07-13 | 2020-08-14 | Сирос Фармасьютикалз, Инк. | Ингибиторы циклин-зависимой киназы 7 (cdk7) |
EP3740206B1 (en) | 2018-01-16 | 2024-03-06 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
WO2019143719A1 (en) | 2018-01-16 | 2019-07-25 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
CN113677346A (zh) * | 2018-11-01 | 2021-11-19 | 希洛斯医药品股份有限公司 | 周期蛋白依赖性激酶7(cdk7)的抑制剂 |
EP4051282A4 (en) * | 2019-10-29 | 2023-12-13 | Syros Pharmaceuticals, Inc. | METHOD FOR TREATING CANCER IN BIOMARRKER-IDENTIFIED PATIENTS USING CYCLIN-DEPENDENT KINASE 7 (CDK7) INHIBITORS |
CA3180314A1 (en) * | 2020-05-29 | 2021-12-02 | John Graeme HODGSON | Methods of treating cancer in patients with an anomalous kras gene or deletions within chromosome 9 |
CN112661745A (zh) * | 2020-07-24 | 2021-04-16 | 浙江同源康医药股份有限公司 | 用作cdk7激酶抑制剂的化合物及其应用 |
TW202214600A (zh) * | 2020-09-24 | 2022-04-16 | 大陸商廣州費米子科技有限責任公司 | 嘧啶基衍生物、其製備方法及其用途 |
CA3195794A1 (en) * | 2020-10-16 | 2022-04-21 | Syros Pharmaceuticals, Inc. | Dosing regimens for cyclin?dependent kinase 7 (cdk7) inhibitors |
WO2022089444A1 (zh) * | 2020-10-28 | 2022-05-05 | 恒元生物医药科技(苏州)有限公司 | 一种含氮杂环化合物及其应用 |
CN116670123A (zh) | 2020-12-24 | 2023-08-29 | 湃隆生物科技有限公司(香港) | 芳香杂环类化合物、药物组合物及其应用 |
CA3214517A1 (en) * | 2021-04-10 | 2022-10-13 | Daniel Gold | Voruciclib dosing regimens and methods of treatment including the same |
WO2023014817A1 (en) * | 2021-08-03 | 2023-02-09 | Syros Pharmaceuticals, Inc. | Compositions and methods for treating lymphomas with a cdk7 inhibitor in combination with a btk inhibitor |
WO2023040998A1 (en) * | 2021-09-17 | 2023-03-23 | Taizhou Eoc Pharma Co., Ltd. | A cyclin-dependent kinase inhibitor |
WO2023049691A1 (en) * | 2021-09-23 | 2023-03-30 | Zeno Management, Inc. | Cdk7 inhibitors and methods of treating cancer |
WO2023078451A1 (zh) * | 2021-11-05 | 2023-05-11 | 浙江同源康医药股份有限公司 | 用作cdk7激酶抑制剂的化合物及其应用 |
WO2023109876A1 (en) * | 2021-12-16 | 2023-06-22 | Edigene Therapeutics (Beijing) Inc. | Biomarkers for colorectal cancer treatment |
EP4455132A1 (en) | 2021-12-22 | 2024-10-30 | Insilico Medicine IP Limited | Pyrimidine heterocyclic compound, preparation method therefor and use thereof in medicine |
PE20242008A1 (es) | 2021-12-30 | 2024-10-03 | Biomea Fusion Inc | Compuestos de pirazina como inhibidores de flt3 |
CN114736204A (zh) * | 2022-05-06 | 2022-07-12 | 湖北工业大学 | 一种培西达替尼结构类似物的制备方法及其抗肿瘤中的应用 |
WO2023246371A1 (zh) * | 2022-06-24 | 2023-12-28 | 中国科学院基础医学与肿瘤研究所(筹) | 具有嘧啶并噻吩结构的小分子化合物及其应用 |
CN117384135A (zh) * | 2022-07-04 | 2024-01-12 | 浙江同源康医药股份有限公司 | 用作cdk7激酶抑制剂的化合物及其应用 |
WO2024097179A1 (en) * | 2022-11-02 | 2024-05-10 | Vincerx Pharma, Inc. | Combination therapies comprising a cdk9 inhibitor for cancer |
CN116082337B (zh) * | 2023-03-16 | 2023-06-23 | 英矽智能科技(上海)有限公司 | 炔基取代的杂环化合物,其制法与医药上的用途 |
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