WO2016123054A3 - Kinase drug combinations and methods of use thereof - Google Patents
Kinase drug combinations and methods of use thereof Download PDFInfo
- Publication number
- WO2016123054A3 WO2016123054A3 PCT/US2016/014831 US2016014831W WO2016123054A3 WO 2016123054 A3 WO2016123054 A3 WO 2016123054A3 US 2016014831 W US2016014831 W US 2016014831W WO 2016123054 A3 WO2016123054 A3 WO 2016123054A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inhibitor
- methods
- kinase
- drug combinations
- inhibiting
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- 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
- A61K31/7064—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
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present disclosure relates to method for inhibiting cancer cell growth or inducing apoptosis in cancer cells by inhibiting kinome reprogramming in a combination therapy involving kinase inhibitors. A kinase inhibitor in combination with a P-TEFb inhibitor and/or p300/CBP inhibitor provides a stable growth suppression of the cancer cells, blocking kinome reprogramming response to kinase inhibitors.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562107788P | 2015-01-26 | 2015-01-26 | |
| US62/107,788 | 2015-01-26 | ||
| US201562144457P | 2015-04-08 | 2015-04-08 | |
| US62/144,457 | 2015-04-08 | ||
| US201562195435P | 2015-07-22 | 2015-07-22 | |
| US62/195,435 | 2015-07-22 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2016123054A2 WO2016123054A2 (en) | 2016-08-04 |
| WO2016123054A3 true WO2016123054A3 (en) | 2016-10-20 |
Family
ID=56544522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2016/014831 Ceased WO2016123054A2 (en) | 2015-01-26 | 2016-01-26 | Kinase drug combinations and methods of use thereof |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2016123054A2 (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2007345526B2 (en) | 2007-02-01 | 2013-02-28 | Resverlogix Corp. | Compounds for the prevention and treatment of cardiovascular diseases |
| KR101709492B1 (en) | 2009-03-18 | 2017-02-23 | 리스버로직스 코퍼레이션 | Novel anti-inflammatory agents |
| KR102662814B1 (en) | 2015-03-13 | 2024-05-03 | 리스버로직스 코퍼레이션 | Compositions and treatment methods for treating complement-related diseases |
| ES3010661T3 (en) | 2016-02-26 | 2025-04-04 | Univ Leland Stanford Junior | Pi-kinase inhibitors with anti-infective activity |
| MX2019002121A (en) | 2016-08-23 | 2019-08-12 | Genentech Inc | Combination therapy for the treatment of pancreatic cancer. |
| WO2018078922A1 (en) * | 2016-10-24 | 2018-05-03 | 国立大学法人福井大学 | Preventive agent and therapeutic agent for cataracts, and use of hat inhibitor for production thereof |
| WO2018081830A1 (en) * | 2016-10-31 | 2018-05-03 | Oregon Health & Science University | Combinations of agents to treat hematological malignancies |
| MX393780B (en) | 2017-01-17 | 2025-03-24 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| WO2018170464A1 (en) * | 2017-03-17 | 2018-09-20 | The Johns Hopkins University | Targeted epigenetic therapy against distal regulatory element of tgfb2 expression |
| WO2020055698A1 (en) * | 2018-09-12 | 2020-03-19 | Denovo Biopharma Llc | Combination of enzastaurin and inhibitors of btk and uses thereof |
| WO2020146657A1 (en) * | 2019-01-11 | 2020-07-16 | The Board Of Trustees Of The Leland Stanford Junior University | Pi4-kinase inhibitors with anti-cancer activity |
| AU2020241869B2 (en) | 2019-03-21 | 2025-02-13 | The Board Of Trustees Of The Leland Stanford Junior University | PI4-kinase inhibitors and methods of using the same |
| CA3153456A1 (en) | 2019-10-02 | 2021-04-08 | Stefanie Fluckiger-Mangual | Heterocyclic derivatives, pharmaceutical compositions and their use in the treatment or amelioration of cancer |
| CN111012774A (en) * | 2020-03-02 | 2020-04-17 | 南通大学附属医院 | Application of JQ-1 in preparation of pancreatic cancer treatment drug and verification method for inhibiting secretion of pancreatic cancer exosomes |
| CA3184076A1 (en) * | 2020-06-25 | 2021-12-30 | Stefanie Fluckiger-Mangual | Combination of a cbp/p300 bromodomain inhibitor and a kras inhibitor for the treatment of cancer |
| WO2021260109A1 (en) * | 2020-06-25 | 2021-12-30 | Tolremo Therapeutics Ag | A COMBINATION OF A CBP/p300 BROMODOMAIN INHIBITOR AND AN EGFR INHIBITOR FOR USE IN TREATING EGFR-MUTANT NSCLC |
| CN113318105B (en) * | 2021-05-31 | 2023-02-03 | 新乡医学院 | Medicinal composition containing Binimetinib for treating colon cancer and application thereof |
| EP4376839A4 (en) * | 2021-07-26 | 2025-10-15 | Vincerx Pharma Inc | SELECTIVE CDK9 INHIBITOR FOR THE TREATMENT OF RAS-MUTANT CANCER |
| CN113521035B (en) * | 2021-08-05 | 2023-04-25 | 河南大学 | Preparation method and application of nano-medicine for combined chemoimmunotherapy |
| WO2025072961A1 (en) * | 2023-09-29 | 2025-04-03 | Leapfrog Bio, Inc. | P110 inhibitors for the treatment of cancer |
| CN118593509A (en) * | 2024-06-21 | 2024-09-06 | 福建医科大学附属第一医院 | Use of filgotinib as a sensitizer for the anti-triple-negative breast cancer drug BBDI |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090215793A1 (en) * | 2005-05-13 | 2009-08-27 | Novartis Ag | Methods for treating drug resistant cancer |
| US20100168228A1 (en) * | 2006-10-13 | 2010-07-01 | Reliance Life Sciences Pvt. Ltd. | Novel chemotherapeutic agents against inflammation and cancer |
| WO2012138739A2 (en) * | 2011-04-06 | 2012-10-11 | Chemo-Enhanced Llc | Compositions and methods for treating cancer |
| WO2013026890A1 (en) * | 2011-08-22 | 2013-02-28 | Lead Discovery Center Gmbh | Susceptibility to selective cdk9 inhibitors |
| WO2013148114A1 (en) * | 2012-03-30 | 2013-10-03 | University Of Florida Research Foundation, Inc. | P300/cbp inhibitors and methods of use |
-
2016
- 2016-01-26 WO PCT/US2016/014831 patent/WO2016123054A2/en not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090215793A1 (en) * | 2005-05-13 | 2009-08-27 | Novartis Ag | Methods for treating drug resistant cancer |
| US20100168228A1 (en) * | 2006-10-13 | 2010-07-01 | Reliance Life Sciences Pvt. Ltd. | Novel chemotherapeutic agents against inflammation and cancer |
| WO2012138739A2 (en) * | 2011-04-06 | 2012-10-11 | Chemo-Enhanced Llc | Compositions and methods for treating cancer |
| WO2013026890A1 (en) * | 2011-08-22 | 2013-02-28 | Lead Discovery Center Gmbh | Susceptibility to selective cdk9 inhibitors |
| WO2013148114A1 (en) * | 2012-03-30 | 2013-10-03 | University Of Florida Research Foundation, Inc. | P300/cbp inhibitors and methods of use |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2016123054A2 (en) | 2016-08-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2016123054A3 (en) | Kinase drug combinations and methods of use thereof | |
| PH12018500792A1 (en) | Benzolactam compounds as protein kinase inhibitors | |
| PH12017501155B1 (en) | Thieno [2,3-c] pyrrol-4-one derivatives as erk inhibitors | |
| AU2013323736A8 (en) | Multiple kinase pathway inhibitors | |
| WO2017075629A3 (en) | Wee 1 kinase inhibitors and methods of making and using the same | |
| MX339937B (en) | Compounds and compositions as c-kit kinase inhibitors. | |
| MX2019001125A (en) | Macrocycle kinase inhibitors. | |
| PH12014500351B1 (en) | COMPOUNDS AND COMPOSITIONS AS c-KIT KINASE INHIBITORS | |
| HK1245247A1 (en) | Inhibitors of bromodomains | |
| MD20170016A2 (en) | Aminopyrimidinyl compounds as JAK inhibitors | |
| HK1245677A1 (en) | Heterocyclic itk inhibitors for treating inflammation and cancer | |
| PH12016500330A1 (en) | Certain chemical entities, compositions, and methods | |
| SG10201902074UA (en) | Heterocyclic compounds and uses thereof | |
| TN2013000348A1 (en) | Compounds and compositions as trk inhibitors | |
| MY169987A (en) | Selective pi3k delta inhibitors | |
| CA2983481A1 (en) | Janus kinase inhibitor | |
| MX2014002486A (en) | Compounds and compositions as pdgfr kinase inhibitors. | |
| PH12015502698A1 (en) | Dual selective pi3 delta and gamma kinase inhibitors | |
| HK1221144A1 (en) | Combination therapy comprising a tor kinase inhibitor and a cytidine analog for treating cancer | |
| WO2013134407A3 (en) | Procaspase 3 activation by combination therapy | |
| WO2016073771A3 (en) | Pyrrolopyrimidine derivatives as mps1/ttk kinase inhibitors | |
| EP3390364A4 (en) | Small molecules for inhibiting chemokine activity, a kinase activity and/or cancer cells growth | |
| WO2016106357A8 (en) | Combination of raf inhibitors and aurora kinase inhibitors | |
| WO2014038881A3 (en) | Protein kinase inhibitor comprising pyridine derivatives | |
| HK40015050A (en) | Methods and compositions for use of therapeutic t cells in combination with kinase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 16743930 Country of ref document: EP Kind code of ref document: A2 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 16743930 Country of ref document: EP Kind code of ref document: A2 |