RU2016140626A - Комбинация ингибитора EGFR и ингибитора MEK для применения в лечении рака, вызванного мутировавшим NRAS - Google Patents
Комбинация ингибитора EGFR и ингибитора MEK для применения в лечении рака, вызванного мутировавшим NRAS Download PDFInfo
- Publication number
- RU2016140626A RU2016140626A RU2016140626A RU2016140626A RU2016140626A RU 2016140626 A RU2016140626 A RU 2016140626A RU 2016140626 A RU2016140626 A RU 2016140626A RU 2016140626 A RU2016140626 A RU 2016140626A RU 2016140626 A RU2016140626 A RU 2016140626A
- Authority
- RU
- Russia
- Prior art keywords
- egfr inhibitor
- inhibitor
- nras
- use according
- paragraphs
- Prior art date
Links
- 229940121647 egfr inhibitor Drugs 0.000 title claims 13
- 102100039788 GTPase NRas Human genes 0.000 title claims 6
- 101000744505 Homo sapiens GTPase NRas Proteins 0.000 title claims 6
- 229940124647 MEK inhibitor Drugs 0.000 title claims 4
- 239000002829 mitogen activated protein kinase inhibitor Substances 0.000 title claims 4
- 206010028980 Neoplasm Diseases 0.000 title claims 3
- 201000011510 cancer Diseases 0.000 title claims 3
- 150000003839 salts Chemical class 0.000 claims 5
- 229960003278 osimertinib Drugs 0.000 claims 3
- DUYJMQONPNNFPI-UHFFFAOYSA-N osimertinib Chemical compound COC1=CC(N(C)CCN(C)C)=C(NC(=O)C=C)C=C1NC1=NC=CC(C=2C3=CC=CC=C3N(C)C=2)=N1 DUYJMQONPNNFPI-UHFFFAOYSA-N 0.000 claims 3
- 101150073096 NRAS gene Proteins 0.000 claims 2
- 230000035772 mutation Effects 0.000 claims 2
- HUFOZJXAKZVRNJ-UHFFFAOYSA-N n-[3-[[2-[4-(4-acetylpiperazin-1-yl)-2-methoxyanilino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]phenyl]prop-2-enamide Chemical compound COC1=CC(N2CCN(CC2)C(C)=O)=CC=C1NC(N=1)=NC=C(C(F)(F)F)C=1NC1=CC=CC(NC(=O)C=C)=C1 HUFOZJXAKZVRNJ-UHFFFAOYSA-N 0.000 claims 2
- 229950009855 rociletinib Drugs 0.000 claims 2
- 102200006531 rs121913529 Human genes 0.000 claims 2
- 102200006540 rs121913530 Human genes 0.000 claims 2
- 102200006651 rs121917756 Human genes 0.000 claims 2
- 229950010746 selumetinib Drugs 0.000 claims 2
- CYOHGALHFOKKQC-UHFFFAOYSA-N selumetinib Chemical group OCCONC(=O)C=1C=C2N(C)C=NC2=C(F)C=1NC1=CC=C(Br)C=C1Cl CYOHGALHFOKKQC-UHFFFAOYSA-N 0.000 claims 2
- 102000001301 EGF receptor Human genes 0.000 claims 1
- 108060006698 EGF receptor Proteins 0.000 claims 1
- 239000005411 L01XE02 - Gefitinib Substances 0.000 claims 1
- 239000005551 L01XE03 - Erlotinib Substances 0.000 claims 1
- 206010029260 Neuroblastoma Diseases 0.000 claims 1
- 108091000080 Phosphotransferase Proteins 0.000 claims 1
- 102000001253 Protein Kinase Human genes 0.000 claims 1
- 229960001686 afatinib Drugs 0.000 claims 1
- ULXXDDBFHOBEHA-CWDCEQMOSA-N afatinib Chemical compound N1=CN=C2C=C(O[C@@H]3COCC3)C(NC(=O)/C=C/CN(C)C)=CC2=C1NC1=CC=C(F)C(Cl)=C1 ULXXDDBFHOBEHA-CWDCEQMOSA-N 0.000 claims 1
- ACWZRVQXLIRSDF-UHFFFAOYSA-N binimetinib Chemical compound OCCONC(=O)C=1C=C2N(C)C=NC2=C(F)C=1NC1=CC=C(Br)C=C1F ACWZRVQXLIRSDF-UHFFFAOYSA-N 0.000 claims 1
- 229960002271 cobimetinib Drugs 0.000 claims 1
- RESIMIUSNACMNW-BXRWSSRYSA-N cobimetinib fumarate Chemical compound OC(=O)\C=C\C(O)=O.C1C(O)([C@H]2NCCCC2)CN1C(=O)C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F.C1C(O)([C@H]2NCCCC2)CN1C(=O)C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F RESIMIUSNACMNW-BXRWSSRYSA-N 0.000 claims 1
- 229960001433 erlotinib Drugs 0.000 claims 1
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 claims 1
- 229960002584 gefitinib Drugs 0.000 claims 1
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical group C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 claims 1
- 239000003226 mitogen Substances 0.000 claims 1
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims 1
- 102000020233 phosphotransferase Human genes 0.000 claims 1
- 108060006633 protein kinase Proteins 0.000 claims 1
- 102000016914 ras Proteins Human genes 0.000 claims 1
- 230000001105 regulatory effect Effects 0.000 claims 1
- 102200006537 rs121913529 Human genes 0.000 claims 1
- 102200006539 rs121913529 Human genes 0.000 claims 1
- 102200006538 rs121913530 Human genes 0.000 claims 1
- 102200006541 rs121913530 Human genes 0.000 claims 1
- LIRYPHYGHXZJBZ-UHFFFAOYSA-N trametinib Chemical compound CC(=O)NC1=CC=CC(N2C(N(C3CC3)C(=O)C3=C(NC=4C(=CC(I)=CC=4)F)N(C)C(=O)C(C)=C32)=O)=C1 LIRYPHYGHXZJBZ-UHFFFAOYSA-N 0.000 claims 1
- 229960004066 trametinib Drugs 0.000 claims 1
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 1
- 230000003612 virological effect Effects 0.000 claims 1
Classifications
-
- 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
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4458—Non condensed piperidines, e.g. piperocaine only substituted in position 2, e.g. methylphenidate
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
- A61K48/005—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered
- A61K48/0058—Nucleic acids adapted for tissue specific expression, e.g. having tissue specific promoters as part of a contruct
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Claims (8)
1. Ингибитор EGFR (рецептор эпидермального фактора роста) для применения в лечении рака, вызванного мутировавшим NRAS (вирусный онкоген RAS нейробластомы), где ингибитор EGFR вводят в комбинации с ингибитором MEK (MAP (митогенактивируемая) протеинкиназа/регулируемая внеклеточными сигналами киназа-киназа), и мутация NRAS выбрана из E63K, G12V, G12R, G12A, G12D, G12S и G12C или роста копийности гена NRAS.
2. Ингибитор EGFR для применения по п. 1, где ингибитор EGFR выбран из гефитиниба, эрлотиниба, афатиниба, AZD9291 и CO1686 или их фармацевтически приемлемой соли.
3. Ингибитор EGFR для применения по пп. 1 или 2, где ингибитор EGFR выбран из AZD9291 и CO1686 или их фармацевтически приемлемой соли.
4. Ингибитор EGFR для применения по любому из пп. 1-3, где ингибитор MEK выбран из селуметиниба, траметиниба, MEK-162 и кобиметиниба или их фармацевтически приемлемой соли.
5. Ингибитор EGFR для применения по любому из пп. 1-4, где рак, вызванный мутировавшим NRAS, представляет собой вызванный мутировавшим NRAS немелкоклеточный рак легких.
6. Ингибитор EGFR для применения по любому из пп. 1-5, где мутация NRAS выбрана из E63K, G12V и G12R или роста копийности гена NRAS.
7. Ингибитор EGFR для применения по любому из пп. 1-6, где ингибитор EGFR представляет собой AZD9291 или его фармацевтически приемлемую соль.
8. Ингибитор EGFR для применения по любому из пп. 1-7, где ингибитор MEK представляет собой селуметиниб или его фармацевтически приемлемую соль.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461975088P | 2014-04-04 | 2014-04-04 | |
US61/975,088 | 2014-04-04 | ||
US201462013573P | 2014-06-18 | 2014-06-18 | |
US62/013,573 | 2014-06-18 | ||
PCT/GB2015/051042 WO2015150826A1 (en) | 2014-04-04 | 2015-04-02 | Combination of egfr inhibitor and mek inhibitor for use in the treatment of nras mutated cancer |
Publications (3)
Publication Number | Publication Date |
---|---|
RU2016140626A true RU2016140626A (ru) | 2018-05-07 |
RU2016140626A3 RU2016140626A3 (ru) | 2018-10-23 |
RU2683276C2 RU2683276C2 (ru) | 2019-03-27 |
Family
ID=52824498
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2016140626A RU2683276C2 (ru) | 2014-04-04 | 2015-04-02 | Комбинация ингибитора EGFR и ингибитора MEK для применения в лечении рака, вызванного мутировавшим NRAS |
Country Status (15)
Country | Link |
---|---|
US (2) | US20200237758A1 (ru) |
EP (1) | EP3125885B1 (ru) |
JP (1) | JP6549147B2 (ru) |
KR (1) | KR102406334B1 (ru) |
CN (1) | CN106456774A (ru) |
AU (1) | AU2015242407B2 (ru) |
CA (1) | CA2943402C (ru) |
DK (1) | DK3125885T3 (ru) |
ES (1) | ES2890556T3 (ru) |
HU (1) | HUE055747T2 (ru) |
MA (1) | MA39841A (ru) |
MX (1) | MX369111B (ru) |
PL (1) | PL3125885T3 (ru) |
RU (1) | RU2683276C2 (ru) |
WO (1) | WO2015150826A1 (ru) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2780168C1 (ru) * | 2019-02-18 | 2022-09-20 | Корея Инститьют Оф Сайенс Энд Текнолоджи | Новое производное пиридо [3,4-d] пиримидин-8-она, обладающее ингибирующей протеинкиназы активностью, и фармацевтическая композиция для предупреждения, облегчения или лечения рака, содержащее указанное выше |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017205459A1 (en) | 2016-05-26 | 2017-11-30 | Kalyra Pharmaceuticals, Inc. | Egfr inhibitor compounds |
WO2018218633A1 (en) * | 2017-06-02 | 2018-12-06 | Beijing Percans Oncology Co. Ltd. | Combination therapies for treating cancers |
WO2019195959A1 (en) | 2018-04-08 | 2019-10-17 | Cothera Biosciences, Inc. | Combination therapy for cancers with braf mutation |
CN112218634A (zh) * | 2018-04-09 | 2021-01-12 | G1治疗公司 | 具有驱动致癌突变的癌症的治疗 |
SG11202101397TA (en) | 2018-08-13 | 2021-03-30 | Beijing Percans Oncology Co Ltd | Biomarkers for cancer therapy |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2003221684A1 (en) * | 2002-04-08 | 2003-10-27 | Smithkline Beecham Corporation | Cancer treatment method comprising administering an erb-family inhibitor and a raf and/or ras inhibitor |
EP2355821A1 (en) * | 2008-11-11 | 2011-08-17 | Eli Lilly and Company | P70 s6 kinase inhibitor and egfr inhibitor combination therapy |
ES2654177T3 (es) * | 2011-07-27 | 2018-02-12 | Astrazeneca Ab | Derivados de 2-(2,4,5-anilino sustituido)pirimidina como moduladores de EGFR útiles para tratar el cáncer |
JP6180425B2 (ja) * | 2011-11-23 | 2017-08-23 | メディミューン,エルエルシー | Her3に特異的な結合分子及びそれらの使用 |
US20150071918A1 (en) * | 2012-05-09 | 2015-03-12 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Peptides for the treatment of cancer |
EP2884971A4 (en) * | 2012-08-16 | 2016-01-06 | Ohio State Innovation Foundation | STAT3 INHIBITORS AND ITS USE AGAINST CANCER |
US20140066465A1 (en) * | 2012-09-04 | 2014-03-06 | The Cleveland Clinic Foundation | CANCER TREATMENT USING TYROSINE KINASE AND NF-kB INHIBITORS |
-
2015
- 2015-04-02 CN CN201580022665.5A patent/CN106456774A/zh active Pending
- 2015-04-02 EP EP15715805.6A patent/EP3125885B1/en active Active
- 2015-04-02 CA CA2943402A patent/CA2943402C/en active Active
- 2015-04-02 MA MA039841A patent/MA39841A/fr unknown
- 2015-04-02 HU HUE15715805A patent/HUE055747T2/hu unknown
- 2015-04-02 MX MX2016013048A patent/MX369111B/es active IP Right Grant
- 2015-04-02 PL PL15715805T patent/PL3125885T3/pl unknown
- 2015-04-02 JP JP2016560813A patent/JP6549147B2/ja active Active
- 2015-04-02 DK DK15715805.6T patent/DK3125885T3/da active
- 2015-04-02 KR KR1020167030569A patent/KR102406334B1/ko active Active
- 2015-04-02 AU AU2015242407A patent/AU2015242407B2/en active Active
- 2015-04-02 ES ES15715805T patent/ES2890556T3/es active Active
- 2015-04-02 WO PCT/GB2015/051042 patent/WO2015150826A1/en active Application Filing
- 2015-04-02 RU RU2016140626A patent/RU2683276C2/ru active
- 2015-04-02 US US15/301,448 patent/US20200237758A1/en not_active Abandoned
-
2020
- 2020-12-16 US US17/123,777 patent/US20210177844A1/en not_active Abandoned
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2780168C1 (ru) * | 2019-02-18 | 2022-09-20 | Корея Инститьют Оф Сайенс Энд Текнолоджи | Новое производное пиридо [3,4-d] пиримидин-8-она, обладающее ингибирующей протеинкиназы активностью, и фармацевтическая композиция для предупреждения, облегчения или лечения рака, содержащее указанное выше |
Also Published As
Publication number | Publication date |
---|---|
PL3125885T3 (pl) | 2021-12-06 |
CA2943402A1 (en) | 2015-10-08 |
KR20160135362A (ko) | 2016-11-25 |
CN106456774A (zh) | 2017-02-22 |
RU2683276C2 (ru) | 2019-03-27 |
ES2890556T3 (es) | 2022-01-20 |
EP3125885B1 (en) | 2021-06-30 |
HUE055747T2 (hu) | 2021-12-28 |
MX369111B (es) | 2019-10-29 |
CA2943402C (en) | 2022-12-13 |
US20200237758A1 (en) | 2020-07-30 |
JP2017511341A (ja) | 2017-04-20 |
US20210177844A1 (en) | 2021-06-17 |
AU2015242407A1 (en) | 2016-10-13 |
AU2015242407B2 (en) | 2017-11-09 |
KR102406334B1 (ko) | 2022-06-07 |
MX2016013048A (es) | 2017-04-27 |
EP3125885A1 (en) | 2017-02-08 |
WO2015150826A1 (en) | 2015-10-08 |
JP6549147B2 (ja) | 2019-07-24 |
RU2016140626A3 (ru) | 2018-10-23 |
MA39841A (fr) | 2017-02-08 |
DK3125885T3 (da) | 2021-09-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2016140626A (ru) | Комбинация ингибитора EGFR и ингибитора MEK для применения в лечении рака, вызванного мутировавшим NRAS | |
CY1124680T1 (el) | Παραγωγα 8-[6-[3-(αμινο)προποξυ]-3-πυριδυλο]-1-ισοπροπυλο-ιμιδαζο[4,5-c]κινολιν-2-ονης ως εκλεκτiκοι ρυθμιστες κινασης μεταλλαγμενης αταξιας τελαγγειεκτασιας (atm) για τη θεραπευτικη αγωγη του καρκινου | |
CY1121195T1 (el) | Παραγωγα τετραϋδροναφθαλενιου που αναστελλουνπρωτεϊνη mcl-1 | |
CY1122737T1 (el) | Ενωσεις και συνθεσεις για ρυθμιση δραστικοτητων κινασης μεταλλακτικου εgfr | |
CY1126056T1 (el) | Νεα παραγωγα αμινοπυριμιδινης | |
RU2017131430A (ru) | Способ лечения рака, ассоциированного с мутацией ras | |
HRP20210338T1 (hr) | Kombinacije fgfr-i cmet-inhibitora za liječenje raka | |
JP2015518894A5 (ru) | ||
TN2017000486A1 (en) | Polycyclic amide derivatives as cdk9 inhibitors | |
CY1116231T1 (el) | ΑΛΑΤΑ ΥΠΟΚΑΤΕΣΤΗΜΕΝΗΣ 2,3-ΔIYΔPOΪMIΔAZO[l,2-C] ΚΙΝΑΖΟΛΙΝΗΣ | |
JP2016533379A5 (ru) | ||
PH12015501326A1 (en) | 2 - (2, 4, 5 - substituted -anilino) pyrimidine derivatives as egfr modulators useful for treating cancer | |
JP2015508103A5 (ru) | ||
EA200970700A1 (ru) | Ингибиторы киназы, пригодные для лечения миелопролиферативных заболеваний и других пролиферативных заболеваний | |
JP2014503821A5 (ru) | ||
UA113658C2 (xx) | Кристалічна форма і дималеатного інгібітору тирозинкінази і способи її одержання | |
RU2012124811A (ru) | СПОСОБ ЛЕЧЕНИЯ ПРОЛИФЕРАТИВНЫХ НАРУШЕНИЙ И ДРУГИХ ПАТОЛОГИЧЕСКИХ СОСТОЯНИЙ, ОПОСРЕДОВАННЫХ АКТИВНОСТЬЮ КИНАЗ Bcr-Abl, c-Kit, DDR1, DDR2, ИЛИ PDGF-R | |
EA201690741A1 (ru) | Составы (s)-3-(4-((4-(морфолинометил)бензил)окси)-1-оксоизоиндолин-2-ил)пиперидин-2,6-диона | |
JP2017514806A5 (ru) | ||
BR112018074941A2 (pt) | combinações farmacêuticas | |
BR112015021586A2 (pt) | formulações de morfina | |
CY1122436T1 (el) | Αντισωματα εναντι του υποδοχεα του επιδερμικου αυξητικου παραγοντα (egfr) | |
Hyman et al. | Abstract CT001: Neratinib in HER2 or HER3 mutant solid tumors: SUMMIT, a global, multi-histology, open-label, phase 2" basket" study | |
JP2018536682A5 (ru) | ||
EA202090385A1 (ru) | Новые промежуточные соединения, используемые для синтеза производных аминопиримидина, способ их получения и способ получения производных аминопиримидина с их использованием |