WO2009036082A3 - Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use - Google Patents
Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use Download PDFInfo
- Publication number
- WO2009036082A3 WO2009036082A3 PCT/US2008/075883 US2008075883W WO2009036082A3 WO 2009036082 A3 WO2009036082 A3 WO 2009036082A3 US 2008075883 W US2008075883 W US 2008075883W WO 2009036082 A3 WO2009036082 A3 WO 2009036082A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- combinations
- methods
- chemotherapeutic agents
- inhibitor compounds
- phosphoinositide
- 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
- A61K31/535—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
- 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
-
- 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
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HK10111710.4A HK1145287B (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| RU2010112837/15A RU2523890C2 (en) | 2007-09-12 | 2008-09-10 | Combinations of inhibitors of phosphoinositide 3-kinase and chemiotherapeutic agents and methods of application |
| EP08799418.2A EP2205242B1 (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| ES08799418.2T ES2537352T3 (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods for their use |
| CN200880116412.4A CN101939006B (en) | 2007-09-12 | 2008-09-10 | Phosphoinositide 3-kinase inhibitor compounds is combined and using method with chemotherapeutics |
| MX2010002543A MX338504B (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use. |
| CA2699202A CA2699202C (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| JP2010524965A JP5658565B2 (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents and methods of use |
| BRPI0816769A BRPI0816769A2 (en) | 2007-09-12 | 2008-09-10 | combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| AU2008298948A AU2008298948B2 (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| IL204333A IL204333A (en) | 2007-09-12 | 2010-03-07 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents |
| ZA2010/02475A ZA201002475B (en) | 2007-09-12 | 2010-04-08 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents,and methods of use |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97177307P | 2007-09-12 | 2007-09-12 | |
| US60/971,773 | 2007-09-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2009036082A2 WO2009036082A2 (en) | 2009-03-19 |
| WO2009036082A3 true WO2009036082A3 (en) | 2009-11-19 |
Family
ID=39942941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2008/075883 Ceased WO2009036082A2 (en) | 2007-09-12 | 2008-09-10 | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US8247397B2 (en) |
| EP (1) | EP2205242B1 (en) |
| JP (1) | JP5658565B2 (en) |
| KR (1) | KR101584823B1 (en) |
| CN (1) | CN101939006B (en) |
| AR (1) | AR068402A1 (en) |
| AU (1) | AU2008298948B2 (en) |
| BR (1) | BRPI0816769A2 (en) |
| CA (1) | CA2699202C (en) |
| CL (1) | CL2008002687A1 (en) |
| ES (1) | ES2537352T3 (en) |
| IL (1) | IL204333A (en) |
| MX (1) | MX338504B (en) |
| PE (2) | PE20140100A1 (en) |
| RU (1) | RU2523890C2 (en) |
| TW (1) | TWI471134B (en) |
| WO (1) | WO2009036082A2 (en) |
| ZA (1) | ZA201002475B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11529350B2 (en) | 2019-07-03 | 2022-12-20 | Sumitomo Pharma Oncology, Inc. | Tyrosine kinase non-receptor 1 (TNK1) inhibitors and uses thereof |
Families Citing this family (259)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
| US20030133939A1 (en) | 2001-01-17 | 2003-07-17 | Genecraft, Inc. | Binding domain-immunoglobulin fusion proteins |
| JO3000B1 (en) | 2004-10-20 | 2016-09-05 | Genentech Inc | Antibody Formulations. |
| GB0423653D0 (en) | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| EP1850874B1 (en) | 2005-02-23 | 2013-10-16 | Genentech, Inc. | Extending time to disease progression or survival in ovarian cancer patients using pertuzumab |
| RU2423381C2 (en) | 2005-07-25 | 2011-07-10 | Трабьон Фармасьютикалз, Инк. | Decreasing b-cell count with using cd37-specific and cd20-specific binding molecules |
| NZ573646A (en) | 2006-06-12 | 2012-04-27 | Wyeth Llc | Single-chain multivalent binding proteins with effector function |
| SI2132573T1 (en) | 2007-03-02 | 2014-07-31 | Genentech, Inc. | Predicting response to a her dimerisation inhbitor based on low her3 expression |
| GB0721095D0 (en) * | 2007-10-26 | 2007-12-05 | Piramed Ltd | Pharmaceutical compounds |
| TWI472339B (en) | 2008-01-30 | 2015-02-11 | Genentech Inc | Composition comprising antibody that binds to domain ii of her2 and acidic variants thereof |
| DK2644194T3 (en) * | 2008-03-18 | 2017-07-03 | Genentech Inc | Combinations of an anti-HER2 antibody-drug conjugate and docetaxel |
| RU2531754C2 (en) | 2008-04-11 | 2014-10-27 | ЭМЕРДЖЕНТ ПРОДАКТ ДИВЕЛОПМЕНТ СИЭТЛ,ЭлЭлСи,US | Immunotherapeutic agent combined with cd37, and its combination with bifunctional chemotherapeutic agent |
| BRPI0812682A2 (en) | 2008-06-16 | 2010-06-22 | Genentech Inc | metastatic breast cancer treatment |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| EA024252B1 (en) | 2009-01-08 | 2016-08-31 | Кьюрис, Инк. | Phosphoinositide 3-kinase inhibitors with a zinc binding moiety |
| JP5709766B2 (en) * | 2009-03-12 | 2015-04-30 | ジェネンテック, インコーポレイテッド | Combination of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents for the treatment of hematopoietic tumors |
| SG178986A1 (en) * | 2009-09-08 | 2012-04-27 | Hoffmann La Roche | 4-substituted pyridin-3-yl-carboxamide compounds and methods of use |
| JP2013504325A (en) * | 2009-09-09 | 2013-02-07 | アビラ セラピューティクス, インコーポレイテッド | PI3 kinase inhibitors and uses thereof |
| CA2776944A1 (en) * | 2009-10-12 | 2011-05-12 | F. Hoffmann-La Roche Ag | Combinations of a pi3k inhibitor and a mek inhibitor |
| US20110165155A1 (en) * | 2009-12-04 | 2011-07-07 | Genentech, Inc. | Methods of treating metastatic breast cancer with trastuzumab-mcc-dm1 |
| PH12012501361A1 (en) | 2009-12-31 | 2012-10-22 | Centro Nac De Investigaciones Oncologicas Cnio | Tricyclic compounds for use as kinase inhibitors |
| UY33236A (en) | 2010-02-25 | 2011-09-30 | Novartis Ag | DIMERIC INHIBITORS OF THE IAP |
| KR101461767B1 (en) | 2010-03-30 | 2014-11-13 | 노파르티스 아게 | Pkc inhibitors for the treatment of b-cell lymphoma having chronic active b-cell-receptor signalling |
| WO2011130654A1 (en) * | 2010-04-16 | 2011-10-20 | Genentech, Inc. | Fox03a as predictive biomarker for pi3k/akt kinase pathway inhibitor efficacy |
| US9586996B2 (en) | 2010-04-30 | 2017-03-07 | Esperance Pharmaceuticals, Inc. | Lytic-peptide-Her2/neu (human epidermal growth factor receptor 2) ligand conjugates and methods of use |
| WO2011159726A2 (en) | 2010-06-14 | 2011-12-22 | The Scripps Research Institute | Reprogramming of cells to a new fate |
| AU2011290672B2 (en) | 2010-08-20 | 2015-07-09 | Novartis Ag | Antibodies for epidermal growth factor receptor 3 (HER3) |
| MX2013003599A (en) * | 2010-10-01 | 2013-07-29 | Biogen Idec Inc | Interferon-beta for use as monotherapy or in combination with other cancer therapies. |
| UY33794A (en) | 2010-12-13 | 2012-07-31 | Novartis Ag | DIMERIC INHIBITORS OF THE IAP |
| EP2651917A1 (en) | 2010-12-13 | 2013-10-23 | Novartis AG | Dimeric iap inhibitors |
| WO2012098387A1 (en) | 2011-01-18 | 2012-07-26 | Centro Nacional De Investigaciones Oncológicas (Cnio) | 6, 7-ring-fused triazolo [4, 3 - b] pyridazine derivatives as pim inhibitors |
| WO2012135571A1 (en) | 2011-04-01 | 2012-10-04 | Curis, Inc. | Phosphoinositide 3-kinase inhibitor with a zinc binding moiety |
| RU2013148817A (en) * | 2011-04-01 | 2015-05-10 | Дженентек, Инк. | COMBINATIONS OF ACT AND MEK INHIBITOR COMPOUNDS AND WAYS OF THEIR APPLICATION |
| US20120308562A1 (en) * | 2011-06-03 | 2012-12-06 | Derynck Mika K | Methods of treating mesothelioma with a pi3k inhibitor compound |
| EP2731942B1 (en) | 2011-07-13 | 2015-09-23 | Novartis AG | Novel 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors |
| US9227982B2 (en) | 2011-07-13 | 2016-01-05 | Novartis Ag | 4-oxo-3,5,7,8-tetrahydro-4H-pyrano[4,3-d]pyrminidinyl compounds for use as tankyrase inhibitors |
| AU2012282076A1 (en) | 2011-07-13 | 2014-02-27 | Novartis Ag | 4 - piperidinyl compounds for use as tankyrase inhibitors |
| EP3812387A1 (en) | 2011-07-21 | 2021-04-28 | Sumitomo Dainippon Pharma Oncology, Inc. | Heterocyclic protein kinase inhibitors |
| WO2013019620A2 (en) * | 2011-07-29 | 2013-02-07 | Glaxosmithkline Llc | Method of treating cancer using combination of braf inhibitor, mek inhibitor, and anti-ctla-4 antibody |
| CA2849331A1 (en) | 2011-10-13 | 2013-04-18 | Genentech, Inc. | Treatment of pharmacological-induced hypochlorhydria |
| IL301603A (en) | 2011-10-14 | 2023-05-01 | Genentech Inc | Pertuzumab, Trastuzumab, Docetaxel and Carboplatin for use in neoadjuvant treatment of a patient |
| HK1202333A1 (en) * | 2011-11-11 | 2015-09-25 | Intellikine, Llc | Combination of kinase inhibitors and uses thereof |
| EP2788330A1 (en) | 2011-12-05 | 2014-10-15 | Novartis AG | Cyclic urea derivatives as androgen receptor antagonists |
| CN104105709A (en) | 2011-12-05 | 2014-10-15 | 诺华股份有限公司 | Antibodies for epidermal growth factor receptor 3 (HER3) directed to domain II of HER3 |
| EP3590538A1 (en) | 2011-12-05 | 2020-01-08 | Novartis AG | Antibodies for epidermal growth factor receptor 3 (her3) |
| EP2802658A2 (en) | 2012-01-09 | 2014-11-19 | Novartis AG | Rnai agents to treat beta-catenin related diseases |
| BR112014028376A2 (en) | 2012-06-08 | 2018-04-24 | Hoffmann La Roche | methods for treating a hyperproliferative disorder, for determining compounds, for monitoring, for optimizing therapeutic efficacy and for identifying a biomarker; pharmaceutical formulation; use of a therapeutic combination and gdc-0032, article of manufacture, product and invention |
| WO2013192367A1 (en) | 2012-06-22 | 2013-12-27 | Novartis Ag | Neuroendocrine tumor treatment |
| US8895729B2 (en) | 2012-10-10 | 2014-11-25 | Genentech, Inc. | Process for making thienopyrimidine compounds |
| EP2909181B1 (en) | 2012-10-16 | 2017-08-09 | Tolero Pharmaceuticals, Inc. | Pkm2 modulators and methods for their use |
| JP2016502974A (en) * | 2012-12-07 | 2016-02-01 | ザ ジェネラル ホスピタル コーポレイション | Combinations of PI3K / AKT inhibitor compounds and HER3 / EGFR inhibitor compounds and their use in the treatment of hyperproliferative diseases |
| ES2671516T3 (en) | 2013-02-19 | 2018-06-06 | Novartis Ag | Benzothiophene derivatives and compositions thereof as selective estrogen receptor degraders |
| JP6647868B2 (en) | 2013-02-20 | 2020-02-14 | ノバルティス アーゲー | Treatment of cancer with humanized anti-EGFRvIII chimeric antigen receptor |
| US9498532B2 (en) | 2013-03-13 | 2016-11-22 | Novartis Ag | Antibody drug conjugates |
| MX394360B (en) | 2013-03-14 | 2025-03-24 | Sumitomo Pharma Oncology Inc | JAK2 AND ALK2 INHIBITORS AND METHODS OF THEIR USE. |
| ES2701051T3 (en) | 2013-03-15 | 2019-02-20 | Novartis Ag | Antibody-drug conjugates |
| MX368259B (en) | 2013-04-16 | 2019-09-25 | Genentech Inc | Pertuzumab variants and evaluation thereof. |
| WO2015092634A1 (en) | 2013-12-16 | 2015-06-25 | Novartis Ag | 1,2,3,4-tetrahydroisoquinoline compounds and compositions as selective estrogen receptor antagonists and degraders |
| JO3517B1 (en) | 2014-01-17 | 2020-07-05 | Novartis Ag | N-azaspirocycloalkane substituted n-heteroaryl compounds and compositions for inhibiting the activity of shp2 |
| ES2699351T3 (en) | 2014-01-17 | 2019-02-08 | Novartis Ag | Derivatives of 1-pyridazin / triazin-3-yl-piper (-azine) / idine / pyrolidine and compositions thereof to inhibit the activity of SHP2 |
| WO2015107494A1 (en) | 2014-01-17 | 2015-07-23 | Novartis Ag | 1 -(triazin-3-yi_/pyridazin-3-yl)-piper(-azine)idine derivatives and compositions thereof for inhibiting the activity of shp2 |
| KR20160141857A (en) | 2014-04-25 | 2016-12-09 | 제넨테크, 인크. | Methods of treating early breast cancer with trastuzumab-mcc-dm1 and pertuzumab |
| WO2015177184A1 (en) | 2014-05-21 | 2015-11-26 | F. Hoffmann-La Roche Ag | Methods of treating pr-positive, luminal a breast cancer with pi3k inhibitor, pictilisib |
| EP3392348A3 (en) * | 2014-06-16 | 2018-11-21 | Worldwide Innovative Network | Method for selecting personalized tri-therapy for cancer treatment |
| EP3539990B1 (en) | 2014-07-16 | 2021-09-08 | Dana-Farber Cancer Institute, Inc. | Her3 inhibition in low-grade serous cancers |
| WO2016020791A1 (en) | 2014-08-05 | 2016-02-11 | Novartis Ag | Ckit antibody drug conjugates |
| MA40513A (en) | 2014-08-12 | 2017-06-21 | Novartis Ag | DRUG-ANTIBODY ANTI-CDH6 CONJUGATES |
| KR20170060042A (en) | 2014-09-13 | 2017-05-31 | 노파르티스 아게 | Combination therapies of alk inhibitors |
| KR20170066546A (en) | 2014-10-03 | 2017-06-14 | 노파르티스 아게 | Combination therapies |
| TW201625692A (en) | 2014-11-14 | 2016-07-16 | 諾華公司 | Antibody drug conjugate |
| JP6454419B2 (en) * | 2014-12-11 | 2019-01-16 | ナトコ ファーマ リミテッド | 7- (morpholinyl) -2- (N-piperazinyl) methylthieno [2,3-c] pyridine derivatives as anticancer agents |
| ES2784900T3 (en) | 2014-12-12 | 2020-10-01 | Massachusetts Gen Hospital | Treatment of brain metastases from breast cancer |
| EP3233918A1 (en) | 2014-12-19 | 2017-10-25 | Novartis AG | Combination therapies |
| UY36462A (en) | 2014-12-23 | 2016-07-29 | Novartis Ag | TRIAZOLOPIRIMIDINE COMPOUNDS AND USES OF THE SAME |
| AU2016238436A1 (en) | 2015-03-25 | 2017-08-17 | Novartis Ag | Formylated N-heterocyclic derivatives as FGFR4 inhibitors |
| AR104068A1 (en) | 2015-03-26 | 2017-06-21 | Hoffmann La Roche | COMBINATIONS OF A 3-KINASE PHOSFOINOSYTIDE INHIBITOR COMPOSITE AND A CDK4 / 6 INHIBITOR COMPOUND FOR CANCER TREATMENT |
| WO2016196373A2 (en) | 2015-05-30 | 2016-12-08 | Genentech, Inc. | Methods of treating her2-positive metastatic breast cancer |
| JP6871919B2 (en) | 2015-06-16 | 2021-05-19 | ナノファギックス エルエルシー | Drug Delivery and Imaging Chemical Conjugates, Formulations and Methods of Use |
| US20190194315A1 (en) | 2015-06-17 | 2019-06-27 | Novartis Ag | Antibody drug conjugates |
| WO2016203405A1 (en) | 2015-06-19 | 2016-12-22 | Novartis Ag | Compounds and compositions for inhibiting the activity of shp2 |
| US10287266B2 (en) | 2015-06-19 | 2019-05-14 | Novartis Ag | Compounds and compositions for inhibiting the activity of SHP2 |
| EP3310779B1 (en) | 2015-06-19 | 2019-05-08 | Novartis AG | Compounds and compositions for inhibiting the activity of shp2 |
| HK1249866A1 (en) | 2015-06-29 | 2018-11-16 | 豪夫迈‧罗氏有限公司 | Methods of treatment with taselisib |
| CN105147696A (en) * | 2015-07-08 | 2015-12-16 | 李荣勤 | Anti-breast cancer granules combining metformin hydrochloride and gdc 0941 and a preparation method thereof |
| GB201514760D0 (en) * | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds and method of use |
| WO2017053469A2 (en) | 2015-09-21 | 2017-03-30 | Aptevo Research And Development Llc | Cd3 binding polypeptides |
| EP3368092B9 (en) | 2015-10-29 | 2020-07-29 | Novartis AG | Antibody conjugates comprising toll-like receptor agonist |
| WO2017087280A1 (en) | 2015-11-16 | 2017-05-26 | Genentech, Inc. | Methods of treating her2-positive cancer |
| RU2018123524A (en) | 2015-12-03 | 2020-01-09 | Новартис Аг | PHARMACEUTICAL DIAGNOSTICS |
| DK3452465T3 (en) | 2016-05-04 | 2021-02-08 | Genoscience Pharma | SUBSTITUTED 2,4-DIAMINOQUINOLINE DERIVATIVES FOR USE IN THE TREATMENT OF PROLIFERATIVE DISEASES |
| WO2017216706A1 (en) | 2016-06-14 | 2017-12-21 | Novartis Ag | Compounds and compositions for inhibiting the activity of shp2 |
| EP3472166A1 (en) | 2016-06-20 | 2019-04-24 | Novartis AG | Imidazopyrimidine compounds useful for the treatment of cancer |
| WO2017221092A1 (en) | 2016-06-20 | 2017-12-28 | Novartis Ag | Triazolopyridine compounds and uses thereof |
| ES2975263T3 (en) | 2016-06-20 | 2024-07-04 | Novartis Ag | Crystalline forms of a triazolopyrimidine compound |
| TW201813963A (en) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
| TW201825465A (en) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
| TW201815787A (en) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
| AU2017335634A1 (en) | 2016-09-27 | 2019-03-14 | Cero Therapeutics, Inc. | Chimeric engulfment receptor molecules |
| KR102607967B1 (en) | 2016-12-19 | 2023-11-29 | 메르크 파텐트 게엠베하 | Combination of Protein Kinase Inhibitors and Additional Chemotherapeutic Agents |
| CN110366550A (en) | 2016-12-22 | 2019-10-22 | 美国安进公司 | Benzisothiazole, isothiazolo[3,4-b]pyridine, quinazoline, phthalazine, pyrido[2,3-d as KRAS G12C inhibitors for the treatment of lung, pancreatic or colorectal cancer ]pyridazine and pyrido[2,3-d]pyrimidine derivatives |
| EP3562844A1 (en) | 2016-12-28 | 2019-11-06 | Genentech, Inc. | Treatment of advanced her2 expressing cancer |
| TW202508629A (en) | 2017-01-17 | 2025-03-01 | 美商建南德克公司 | Subcutaneous her2 antibody formulations |
| JOP20190187A1 (en) | 2017-02-03 | 2019-08-01 | Novartis Ag | Anti-ccr7 antibody drug conjugates |
| PT3589661T (en) | 2017-03-02 | 2024-01-29 | Genentech Inc | Adjuvant treatment of her2-positive breast cancer |
| WO2018163051A1 (en) | 2017-03-06 | 2018-09-13 | Novartis Ag | Methods of treatment of cancer with reduced ubb expression |
| WO2018185618A1 (en) | 2017-04-03 | 2018-10-11 | Novartis Ag | Anti-cdh6 antibody drug conjugates and anti-gitr antibody combinations and methods of treatment |
| WO2018200505A1 (en) | 2017-04-24 | 2018-11-01 | Genentech, Inc. | Erbb2/her2 mutations in the transmbrane or juxtamembrane domain |
| AR111651A1 (en) | 2017-04-28 | 2019-08-07 | Novartis Ag | CONJUGATES OF ANTIBODIES THAT INCLUDE TOLL TYPE RECEIVER AGONISTS AND COMBINATION THERAPIES |
| AU2018273356B2 (en) | 2017-05-22 | 2021-09-16 | Amgen Inc. | KRAS G12C inhibitors and methods of using the same |
| WO2018215937A1 (en) | 2017-05-24 | 2018-11-29 | Novartis Ag | Interleukin-7 antibody cytokine engrafted proteins and methods of use in the treatment of cancer |
| WO2018215938A1 (en) | 2017-05-24 | 2018-11-29 | Novartis Ag | Antibody-cytokine engrafted proteins and methods of use |
| MY206158A (en) | 2017-05-24 | 2024-12-02 | Novartis Ag | Antibody-cytokine engrafted proteins and methods of use in the treatment of cancer |
| RU2020108454A (en) | 2017-07-31 | 2021-09-02 | Дзе Трастиз Оф Коламбия Юниверсити Ин Дзе Сити Оф Нью Йорк | COMPOUNDS, COMPOSITIONS AND METHODS FOR T-CELL T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA |
| WO2019027765A1 (en) * | 2017-08-02 | 2019-02-07 | Northwestern University | Substituted fused pyrimidine compounds and uses there |
| AU2018329920B2 (en) | 2017-09-08 | 2022-12-01 | Amgen Inc. | Inhibitors of KRAS G12C and methods of using the same |
| JP7447002B2 (en) | 2017-09-11 | 2024-03-11 | クルーゾン・ファーマシューティカルズ・インコーポレイテッド | Octahydrocyclopenta[c]pyrrole allosteric inhibitor of SHP2 |
| EP4714966A2 (en) | 2017-09-26 | 2026-03-25 | Cero Therapeutics Holdings, Inc. | Chimeric engulfment receptor molecules and methods of use |
| EP3706735A1 (en) * | 2017-11-06 | 2020-09-16 | Snap Bio, Inc. | Pim kinase inhibitor compositions, methods, and uses thereof |
| CN108187055B (en) * | 2018-03-06 | 2019-12-27 | 北京大学 | Anticancer composition with synergistic effect |
| EP3774906A1 (en) | 2018-03-28 | 2021-02-17 | Cero Therapeutics, Inc. | Chimeric tim4 receptors and uses thereof |
| MX2020010241A (en) | 2018-03-28 | 2020-10-16 | Cero Therapeutics Inc | Cellular immunotherapy compositions and uses thereof. |
| CA3093969A1 (en) | 2018-03-28 | 2019-10-03 | Cero Therapeutics, Inc. | Expression vectors for chimeric engulfment receptors, genetically modified host cells, and uses thereof |
| KR20210003780A (en) | 2018-04-05 | 2021-01-12 | 스미토모 다이니폰 파마 온콜로지, 인크. | AXL kinase inhibitors and uses thereof |
| EP3788053B1 (en) | 2018-05-04 | 2024-07-10 | Amgen Inc. | Kras g12c inhibitors and methods of using the same |
| CA3098574A1 (en) | 2018-05-04 | 2019-11-07 | Amgen Inc. | Kras g12c inhibitors and methods of using the same |
| MA52564A (en) | 2018-05-10 | 2021-03-17 | Amgen Inc | KRAS G12C INHIBITORS FOR CANCER TREATMENT |
| US11096939B2 (en) | 2018-06-01 | 2021-08-24 | Amgen Inc. | KRAS G12C inhibitors and methods of using the same |
| MX2020012204A (en) | 2018-06-11 | 2021-03-31 | Amgen Inc | KRAS G12C INHIBITORS TO TREAT CANCER. |
| US11285156B2 (en) | 2018-06-12 | 2022-03-29 | Amgen Inc. | Substituted piperazines as KRAS G12C inhibitors |
| BR122022012697B1 (en) | 2018-07-10 | 2023-04-04 | Novartis Ag | USES OF 3-(5-HYDROXY-1-OXOISOINDOLIN-2-IL)PIPERIDINE-2,6- DIONE DERIVATIVES, AND KIT |
| AR116109A1 (en) | 2018-07-10 | 2021-03-31 | Novartis Ag | DERIVATIVES OF 3- (5-AMINO-1-OXOISOINDOLIN-2-IL) PIPERIDINE-2,6-DIONA AND USES OF THE SAME |
| AU2019310590A1 (en) | 2018-07-26 | 2021-01-14 | Sumitomo Pharma Oncology, Inc. | Methods for treating diseases associated with abnormal acvr1 expression and acvr1 inhibitors for use in the same |
| PT3837256T (en) | 2018-08-17 | 2023-05-23 | Novartis Ag | UREA COMPOUNDS AND COMPOSITIONS AS SMARCA2/BRM-ATPASE INHIBITORS |
| CN113164466B (en) | 2018-09-11 | 2025-07-08 | 柯瑞斯公司 | Combination therapy using phosphoinositide 3-kinase inhibitors having zinc binding moieties |
| CR20210175A (en) | 2018-09-18 | 2021-06-01 | Nikang Therapeutics Inc | Fused tricyclic ring derivatives as src homology-2 phosphatase inhibitors |
| US20220041613A1 (en) | 2018-09-25 | 2022-02-10 | Black Diamond Therapeutics, Inc. | Tyrosine kinase inhibitor compositions, methods of making and methods of use |
| JP2022502495A (en) | 2018-09-25 | 2022-01-11 | ブラック ダイアモンド セラピューティクス,インコーポレイティド | Quinazoline derivatives as tyrosine kinase inhibitors, compositions, methods of their preparation, and their use |
| IL305106B2 (en) | 2018-09-29 | 2025-08-01 | Novartis Ag | Process for producing a compound for inhibiting the activity of SHP2 |
| US20230053449A1 (en) | 2018-10-31 | 2023-02-23 | Novartis Ag | Dc-sign antibody drug conjugates |
| JP7516029B2 (en) | 2018-11-16 | 2024-07-16 | アムジエン・インコーポレーテツド | Improved synthesis of key intermediates for KRAS G12C inhibitor compounds |
| AU2019384118B2 (en) | 2018-11-19 | 2025-06-12 | Amgen Inc. | KRAS G12C inhibitors and methods of using the same |
| JP7377679B2 (en) | 2018-11-19 | 2023-11-10 | アムジエン・インコーポレーテツド | Combination therapy comprising a KRASG12C inhibitor and one or more additional pharmaceutically active agents for the treatment of cancer |
| JP7686559B2 (en) | 2018-12-20 | 2025-06-02 | アムジエン・インコーポレーテツド | KIF18A inhibitor |
| KR20210106437A (en) | 2018-12-20 | 2021-08-30 | 노파르티스 아게 | Dosage regimens and pharmaceutical combinations comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives |
| MA54543A (en) | 2018-12-20 | 2022-03-30 | Amgen Inc | KIF18A INHIBITORS |
| JP2022513967A (en) | 2018-12-20 | 2022-02-09 | アムジエン・インコーポレーテツド | Heteroarylamide useful as a KIF18A inhibitor |
| AU2019401495B2 (en) | 2018-12-20 | 2025-06-26 | Amgen Inc. | Heteroaryl amides useful as KIF18A inhibitors |
| KR20210107731A (en) | 2018-12-21 | 2021-09-01 | 노파르티스 아게 | Antibodies to PMEL17 and conjugates thereof |
| CA3126143A1 (en) * | 2019-01-11 | 2020-07-16 | The Board Of Trustees Of The Leland Stanford Junior University | Pi4-kinase inhibitors with anti-cancer activity |
| KR20260008165A (en) | 2019-02-12 | 2026-01-15 | 스미토모 파마 아메리카, 인크. | Formulations comprising heterocyclic protein kinase inhibitors |
| CN113490528B (en) | 2019-02-15 | 2024-12-03 | 诺华股份有限公司 | 3-(1-oxo-5-(piperidin-4-yl)isoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| CA3123519A1 (en) | 2019-02-15 | 2020-08-20 | Novartis Ag | Substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| MX2021010323A (en) | 2019-03-01 | 2021-12-10 | Revolution Medicines Inc | Bicyclic heterocyclyl compounds and uses thereof. |
| MX2021010319A (en) | 2019-03-01 | 2021-12-10 | Revolution Medicines Inc | Bicyclic heteroaryl compounds and uses thereof. |
| US12415788B2 (en) | 2019-03-21 | 2025-09-16 | The Board Of Trustees Of The Leland Stanford Junior University | PI4-kinase inhibitors and methods of using the same |
| KR20210141621A (en) | 2019-03-22 | 2021-11-23 | 스미토모 다이니폰 파마 온콜로지, 인크. | Compositions comprising PKM2 modulators and methods of treatment using same |
| EP3738593A1 (en) | 2019-05-14 | 2020-11-18 | Amgen, Inc | Dosing of kras inhibitor for treatment of cancers |
| WO2020236947A1 (en) | 2019-05-21 | 2020-11-26 | Amgen Inc. | Solid state forms |
| EP4007756B1 (en) | 2019-08-02 | 2025-12-24 | Amgen Inc. | Kif18a inhibitors |
| EP4007638A1 (en) | 2019-08-02 | 2022-06-08 | Amgen Inc. | Pyridine derivatives as kif18a inhibitors |
| EP4007753B1 (en) | 2019-08-02 | 2025-09-24 | Amgen Inc. | Kif18a inhibitors |
| EP4007752B1 (en) | 2019-08-02 | 2025-09-24 | Amgen Inc. | Kif18a inhibitors |
| AU2020328598A1 (en) | 2019-08-15 | 2022-03-03 | Black Diamond Therapeutics, Inc. | Alkynyl quinazoline compounds |
| US20220402916A1 (en) | 2019-09-18 | 2022-12-22 | Merck Sharp & Dohme Corp. | Small molecule inhibitors of kras g12c mutant |
| JP7763753B2 (en) | 2019-09-26 | 2025-11-04 | ノバルティス アーゲー | Azaquinoline compounds and uses thereof |
| EP4038097A1 (en) | 2019-10-03 | 2022-08-10 | Cero Therapeutics, Inc. | Chimeric tim4 receptors and uses thereof |
| US20240139193A1 (en) | 2019-10-15 | 2024-05-02 | Amgen Inc. | Combination therapy of kras inhibitor and shp2 inhibitor for treatment of cancers |
| EP4048671B1 (en) | 2019-10-24 | 2026-03-18 | Amgen Inc. | Pyridopyrimidine derivatives useful as kras g12c and kras g12d inhibitors in the treatment of cancer |
| UA129778C2 (en) | 2019-10-28 | 2025-07-30 | Мерк Шарп Енд Доум Елелсі | LOW-MOLECULAR INHIBITORS OF G12C-MUTANT KRAS |
| US20230023023A1 (en) | 2019-10-31 | 2023-01-26 | Taiho Pharmaceutical Co., Ltd. | 4-aminobut-2-enamide derivatives and salts thereof |
| AU2020377925A1 (en) | 2019-11-04 | 2022-05-05 | Revolution Medicines, Inc. | Ras inhibitors |
| IL322454A (en) | 2019-11-04 | 2025-09-01 | Revolution Medicines Inc | Ras inhibitors |
| TW202132316A (en) | 2019-11-04 | 2021-09-01 | 美商銳新醫藥公司 | Ras inhibitors |
| CA3156359A1 (en) | 2019-11-08 | 2021-05-14 | Adrian Liam Gill | Bicyclic heteroaryl compounds and uses thereof |
| JP7837865B2 (en) | 2019-11-14 | 2026-03-31 | アムジエン・インコーポレーテツド | Improved synthesis method for KRAS G12C inhibitor compounds |
| JP2023501528A (en) | 2019-11-14 | 2023-01-18 | アムジエン・インコーポレーテツド | Improved Synthesis of KRAS G12C Inhibitor Compounds |
| EP4065231A1 (en) | 2019-11-27 | 2022-10-05 | Revolution Medicines, Inc. | Covalent ras inhibitors and uses thereof |
| WO2021106231A1 (en) | 2019-11-29 | 2021-06-03 | Taiho Pharmaceutical Co., Ltd. | A compound having inhibitory activity against kras g12d mutation |
| US20230028414A1 (en) | 2019-12-16 | 2023-01-26 | Amgen Inc. | Dosing regimen of kras g12c inhibitor |
| BR112022011902A2 (en) | 2019-12-20 | 2022-09-06 | Novartis Ag | COMBINATION THERAPIES |
| CN111057065B (en) * | 2019-12-24 | 2021-04-23 | 沈阳药科大学 | Preparation method and application of thienopyrimidine compound |
| WO2021142026A1 (en) | 2020-01-07 | 2021-07-15 | Revolution Medicines, Inc. | Shp2 inhibitor dosing and methods of treating cancer |
| WO2021195206A1 (en) | 2020-03-24 | 2021-09-30 | Black Diamond Therapeutics, Inc. | Polymorphic forms and related uses |
| WO2021215544A1 (en) | 2020-04-24 | 2021-10-28 | Taiho Pharmaceutical Co., Ltd. | Kras g12d protein inhibitors |
| WO2021215545A1 (en) | 2020-04-24 | 2021-10-28 | Taiho Pharmaceutical Co., Ltd. | Anticancer combination therapy with n-(1-acryloyl-azetidin-3-yl)-2-((1h-indazol-3-yl)amino)methyl)-1h-imidazole-5-carboxamide inhibitor of kras-g12c |
| US20230181756A1 (en) | 2020-04-30 | 2023-06-15 | Novartis Ag | Ccr7 antibody drug conjugates for treating cancer |
| US20240150358A1 (en) * | 2020-06-03 | 2024-05-09 | Kineta, Inc. | Purines and methods of their use |
| JP2023529211A (en) | 2020-06-11 | 2023-07-07 | ノバルティス アーゲー | ZBTB32 inhibitors and uses thereof |
| KR20230027056A (en) | 2020-06-23 | 2023-02-27 | 노파르티스 아게 | Dosage regimen comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives |
| JP2023532122A (en) | 2020-06-29 | 2023-07-26 | ジェネンテック, インコーポレイテッド | Fixed dose combination of pertuzumab plus trastuzumab |
| EP4183395A4 (en) | 2020-07-15 | 2024-07-24 | Taiho Pharmaceutical Co., Ltd. | Pyrimidine compound-containing combination to be used in tumor treatment |
| JP7819176B2 (en) | 2020-08-03 | 2026-02-24 | ノバルティス アーゲー | Heteroaryl-substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| AR123185A1 (en) | 2020-08-10 | 2022-11-09 | Novartis Ag | COMPOUNDS AND COMPOSITIONS TO INHIBIT EZH2 |
| WO2022036287A1 (en) | 2020-08-14 | 2022-02-17 | Cero Therapeutics, Inc. | Anti-cd72 chimeric receptors and uses thereof |
| WO2022036285A1 (en) | 2020-08-14 | 2022-02-17 | Cero Therapeutics, Inc. | Compositions and methods for treating cancer with chimeric tim receptors in combination with inhibitors of poly (adp-ribose) polymerase |
| WO2022036265A1 (en) | 2020-08-14 | 2022-02-17 | Cero Therapeutics, Inc. | Chimeric tim receptors and uses thereof |
| WO2022043556A1 (en) | 2020-08-31 | 2022-03-03 | Novartis Ag | Stable radiopharmaceutical composition |
| EP4204021A1 (en) | 2020-08-31 | 2023-07-05 | Advanced Accelerator Applications International S.A. | Method of treating psma-expressing cancers |
| EP4204020A1 (en) | 2020-08-31 | 2023-07-05 | Advanced Accelerator Applications International S.A. | Method of treating psma-expressing cancers |
| US20250195521A1 (en) | 2020-09-03 | 2025-06-19 | Revolution Medicines, Inc. | Use of sos1 inhibitors to treat malignancies with shp2 mutations |
| CA3194067A1 (en) | 2020-09-15 | 2022-03-24 | Revolution Medicines, Inc. | Ras inhibitors |
| US11685744B2 (en) | 2020-09-21 | 2023-06-27 | Prelude Therapeutics Incorporated | CDK inhibitors and their use as pharmaceuticals |
| TW202237638A (en) | 2020-12-09 | 2022-10-01 | 日商武田藥品工業股份有限公司 | Compositions of guanylyl cyclase c (gcc) antigen binding agents and methods of use thereof |
| TW202237119A (en) | 2020-12-10 | 2022-10-01 | 美商住友製藥腫瘤公司 | Alk-5 inhibitors and uses thereof |
| WO2022140472A1 (en) | 2020-12-22 | 2022-06-30 | Nikang Therapeutics, Inc. | Compounds for degrading cyclin-dependent kinase 2 via ubiquitin proteosome pathway |
| EP4267134A4 (en) * | 2020-12-22 | 2024-11-06 | Novartis AG | PHARMACEUTICAL COMBINATIONS COMPRISING A KRAS G12C INHIBITOR AND USES OF A KRAS G12C INHIBITOR FOR THE TREATMENT OF CANCERS |
| JP7849366B2 (en) | 2020-12-22 | 2026-04-21 | キル・レガー・セラピューティクス・インコーポレーテッド | SOS1 inhibitors and their use |
| WO2022170052A1 (en) | 2021-02-05 | 2022-08-11 | Black Diamond Therapeutics, Inc. | Quinazoline derivatives, pyridopyrimidine derivatives, pyrimidopyrimidine derivatives, and uses thereof |
| AU2022227021A1 (en) | 2021-02-26 | 2023-09-21 | Kelonia Therapeutics, Inc. | Lymphocyte targeted lentiviral vectors |
| TW202304979A (en) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | USES OF ANTI-TGFβ ANTIBODIES AND OTHER THERAPEUTIC AGENTS FOR THE TREATMENT OF PROLIFERATIVE DISEASES |
| TW202309022A (en) | 2021-04-13 | 2023-03-01 | 美商努法倫特公司 | Amino-substituted heterocycles for treating cancers with egfr mutations |
| BR112023021475A2 (en) | 2021-04-16 | 2023-12-19 | Novartis Ag | ANTIBODY-DRUG CONJUGATES AND METHODS FOR PRODUCING THEM |
| JP2024516450A (en) | 2021-05-05 | 2024-04-15 | レボリューション メディシンズ インコーポレイテッド | Covalent RAS inhibitors and uses thereof |
| TW202309052A (en) | 2021-05-05 | 2023-03-01 | 美商銳新醫藥公司 | Ras inhibitors |
| KR20240017811A (en) | 2021-05-05 | 2024-02-08 | 레볼루션 메디슨즈, 인크. | RAS inhibitors for the treatment of cancer |
| AR125874A1 (en) | 2021-05-18 | 2023-08-23 | Novartis Ag | COMBINATION THERAPIES |
| EP4347041A1 (en) | 2021-05-28 | 2024-04-10 | Taiho Pharmaceutical Co., Ltd. | Small molecule inhibitors of kras mutated proteins |
| TW202317589A (en) | 2021-07-14 | 2023-05-01 | 美商尼坎醫療公司 | Alkylidene derivatives as kras inhibitors |
| EP4376874B1 (en) | 2021-07-28 | 2026-03-04 | Cero Therapeutics Holdings, Inc. | Chimeric tim4 receptors and uses thereof |
| AR127308A1 (en) | 2021-10-08 | 2024-01-10 | Revolution Medicines Inc | RAS INHIBITORS |
| US20240294548A1 (en) | 2021-10-12 | 2024-09-05 | Peloton Therapeutics Inc. | Tricyclic sultams and sulfamides as antitumor agents |
| CN119212994A (en) | 2021-12-17 | 2024-12-27 | 建新公司 | Pyrazolopyrazine compounds as SHP2 inhibitors |
| EP4227307A1 (en) | 2022-02-11 | 2023-08-16 | Genzyme Corporation | Pyrazolopyrazine compounds as shp2 inhibitors |
| KR20240156373A (en) | 2022-03-07 | 2024-10-29 | 암젠 인크 | Method for preparing 4-methyl-2-propan-2-yl-pyridine-3-carbonitrile |
| JP2025510572A (en) | 2022-03-08 | 2025-04-15 | レボリューション メディシンズ インコーポレイテッド | Methods for treating immunorefractory lung cancer |
| CN119053595A (en) | 2022-03-28 | 2024-11-29 | 尼坎治疗公司 | Sulfonylamino derivatives as cyclin dependent kinase 2 inhibitors |
| WO2023214325A1 (en) | 2022-05-05 | 2023-11-09 | Novartis Ag | Pyrazolopyrimidine derivatives and uses thereof as tet2 inhibitors |
| CN119790053A (en) | 2022-06-08 | 2025-04-08 | 霖康疗法公司 | Sulfonamide derivatives as cyclin dependent kinase 2 inhibitors |
| WO2023240263A1 (en) | 2022-06-10 | 2023-12-14 | Revolution Medicines, Inc. | Macrocyclic ras inhibitors |
| AU2023314354A1 (en) | 2022-07-26 | 2024-11-21 | Novartis Ag | Crystalline forms of an akr1c3 dependent kars inhibitor |
| AU2023358792A1 (en) | 2022-10-14 | 2025-04-17 | Black Diamond Therapeutics, Inc. | Methods of treating cancers using isoquinoline or 6-aza-quinoline derivatives |
| AU2023375457A1 (en) | 2022-11-11 | 2025-05-01 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway |
| AU2024241633A1 (en) | 2023-03-30 | 2025-11-06 | Revolution Medicines, Inc. | Compositions for inducing ras gtp hydrolysis and uses thereof |
| CR20250420A (en) | 2023-04-07 | 2025-11-20 | Revolution Medicines Inc | MACROCYCLIC RAS INHIBITORS |
| AR132338A1 (en) | 2023-04-07 | 2025-06-18 | Revolution Medicines Inc | RAS INHIBITORS |
| CN121100123A (en) | 2023-04-14 | 2025-12-09 | 锐新医药公司 | Crystalline forms of Ras inhibitors |
| CN121464140A (en) | 2023-04-14 | 2026-02-03 | 锐新医药公司 | Crystalline forms of RAS inhibitors, compositions containing the same, and methods of use thereof |
| TW202508595A (en) | 2023-05-04 | 2025-03-01 | 美商銳新醫藥公司 | Combination therapy for a ras related disease or disorder |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025043187A1 (en) | 2023-08-24 | 2025-02-27 | Otsuka Pharmaceutical Co., Ltd. | Fixed dose combinations of cedazuridine and azacitidine |
| WO2025072462A1 (en) | 2023-09-27 | 2025-04-03 | Nikang Therapeutics, Inc. | Sulfonamide derivatives as cyclin-dependent kinase 2 inhibitors |
| AU2024360465A1 (en) | 2023-10-12 | 2026-04-09 | Revolution Medicines, Inc. | Macrocyclic ras inhibitors |
| AU2024361909A1 (en) | 2023-10-20 | 2026-03-26 | Merck Sharp & Dohme Llc | Small molecule inhibitors of kras proteins |
| TW202527955A (en) | 2023-11-27 | 2025-07-16 | 美商尼坎醫療公司 | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and cyclin-dependent kinase 4 via ubiquitin proteasome pathway |
| WO2025117981A1 (en) | 2023-12-02 | 2025-06-05 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway |
| TW202542151A (en) | 2023-12-22 | 2025-11-01 | 美商銳格醫藥有限公司 | Sos1 inhibitors and uses thereof |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025212828A1 (en) | 2024-04-03 | 2025-10-09 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and cyclin-dependent kinase 4 via ubiquitin proteasome pathway |
| WO2025240536A1 (en) | 2024-05-15 | 2025-11-20 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and/or cyclin-dependent kinase 4 via ubiquitin proteasome pathway |
| TW202547461A (en) | 2024-05-17 | 2025-12-16 | 美商銳新醫藥公司 | Ras inhibitors |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (en) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Therapeutic compositions and methods for managing treatment-related effects |
| WO2026006747A1 (en) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026015825A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Use of ras inhibitor for treating pancreatic cancer |
| WO2026015796A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015790A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015801A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026050446A1 (en) | 2024-08-29 | 2026-03-05 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026072904A2 (en) | 2024-09-26 | 2026-04-02 | Revolution Medicines, Inc. | Compositions and methods for treating lung cancer |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004065391A1 (en) * | 2003-01-23 | 2004-08-05 | Almirall Prodesfarma S.A. | 4-AMINOTHIENO[2,3-d]PYRIMIDINE-6-CARBONITRILE DERIVATIVES AS PDE7 INHIBITORS |
| WO2005094358A2 (en) * | 2004-03-29 | 2005-10-13 | Roswell Park Cancer Institute | Method of treating solid tumors and leukemias using combination therapy of vitamin d and anti-metabolic nucleoside analogs |
| WO2007127175A2 (en) * | 2006-04-26 | 2007-11-08 | F. Hoffmann-La Roche Ag | Pharmaceutical compounds |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6608053B2 (en) | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| WO2005110477A2 (en) | 2004-04-09 | 2005-11-24 | University Of South Florida | Combination therapies for cancer and proliferative angiopathies |
| JP5371426B2 (en) | 2004-07-09 | 2013-12-18 | プロルックス ファーマシューティカルズ コープ. | Methods of using the same in combination with wortmannin analogs and chemotherapeutic agents |
| GB0423653D0 (en) * | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| KR20090021155A (en) | 2006-04-26 | 2009-02-27 | 에프. 호프만-라 로슈 아게 | Pyrimidine Derivatives as PI3K Inhibitors |
| TW200801012A (en) | 2006-04-26 | 2008-01-01 | Piramed Ltd | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| WO2007129161A2 (en) | 2006-04-26 | 2007-11-15 | F. Hoffmann-La Roche Ag | Thieno [3, 2-d] pyrimidine derivative useful as pi3k inhibitor |
| GB0608820D0 (en) | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
| RU2470936C2 (en) | 2006-12-07 | 2012-12-27 | Дженентек, Инк. | Phosphoinositide3-kinase inhibiting compounds and methods for use thereof |
| MX2009005950A (en) | 2006-12-07 | 2009-10-12 | Genentech Inc | Phosphoinositide 3-kinase inhibitor compounds and methods of use. |
| WO2008152394A1 (en) | 2007-06-12 | 2008-12-18 | F.Hoffmann-La Roche Ag | Pharmaceutical compounds |
| WO2008152387A1 (en) | 2007-06-12 | 2008-12-18 | F.Hoffmann-La Roche Ag | Quinazoline derivatives as pi3 kinase inhibitors |
| US7893060B2 (en) | 2007-06-12 | 2011-02-22 | F. Hoffmann-La Roche Ag | Thiazolopyrimidines and their use as inhibitors of phosphatidylinositol-3 kinase |
-
2008
- 2008-09-10 EP EP08799418.2A patent/EP2205242B1/en active Active
- 2008-09-10 TW TW97134764A patent/TWI471134B/en not_active IP Right Cessation
- 2008-09-10 ES ES08799418.2T patent/ES2537352T3/en active Active
- 2008-09-10 MX MX2010002543A patent/MX338504B/en active IP Right Grant
- 2008-09-10 CL CL2008002687A patent/CL2008002687A1/en unknown
- 2008-09-10 CN CN200880116412.4A patent/CN101939006B/en not_active Expired - Fee Related
- 2008-09-10 KR KR1020107007940A patent/KR101584823B1/en not_active Expired - Fee Related
- 2008-09-10 PE PE2013001830A patent/PE20140100A1/en not_active Application Discontinuation
- 2008-09-10 BR BRPI0816769A patent/BRPI0816769A2/en not_active Application Discontinuation
- 2008-09-10 CA CA2699202A patent/CA2699202C/en not_active Expired - Fee Related
- 2008-09-10 WO PCT/US2008/075883 patent/WO2009036082A2/en not_active Ceased
- 2008-09-10 US US12/208,227 patent/US8247397B2/en not_active Expired - Fee Related
- 2008-09-10 AU AU2008298948A patent/AU2008298948B2/en not_active Ceased
- 2008-09-10 JP JP2010524965A patent/JP5658565B2/en not_active Expired - Fee Related
- 2008-09-10 RU RU2010112837/15A patent/RU2523890C2/en not_active IP Right Cessation
- 2008-09-10 AR ARP080103927A patent/AR068402A1/en unknown
- 2008-09-10 PE PE2008001582A patent/PE20090678A1/en not_active Application Discontinuation
-
2010
- 2010-03-07 IL IL204333A patent/IL204333A/en not_active IP Right Cessation
- 2010-04-08 ZA ZA2010/02475A patent/ZA201002475B/en unknown
-
2011
- 2011-05-17 US US13/109,670 patent/US8604014B2/en not_active Expired - Fee Related
-
2013
- 2013-08-28 US US14/012,673 patent/US20130345217A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004065391A1 (en) * | 2003-01-23 | 2004-08-05 | Almirall Prodesfarma S.A. | 4-AMINOTHIENO[2,3-d]PYRIMIDINE-6-CARBONITRILE DERIVATIVES AS PDE7 INHIBITORS |
| WO2005094358A2 (en) * | 2004-03-29 | 2005-10-13 | Roswell Park Cancer Institute | Method of treating solid tumors and leukemias using combination therapy of vitamin d and anti-metabolic nucleoside analogs |
| WO2007127175A2 (en) * | 2006-04-26 | 2007-11-08 | F. Hoffmann-La Roche Ag | Pharmaceutical compounds |
Non-Patent Citations (12)
| Title |
|---|
| "CellTiter-Glo Luminescent Cell Viability Assay (Promega Technical Bulletin TB288)", XP002546486, Retrieved from the Internet <URL:www.promega.com> [retrieved on 20090918] * |
| BERNHARD ERIC J; MCKENNA W GILLIES; HAMILTON ANDREW D; SEBTI SAID M; QIAN YIMIN; WU JUNMIN; MUSCHEL RUTH J: "Inhibiting Ras prenylation increases the radiosensitivity of human tumor cell lines with activating mutations of ras oncogenes", CANCER RESEARCH, vol. 58, no. 8, 15 April 1998 (1998-04-15), pages 1754 - 1761, XP002546489 * |
| BIANCO R, SHIN I, RITTER CH A, YAKES F M, BASSO A, ROSEN N, TSURUTANI J, DENNIS P A, MILLS G B, ARTEAGA C L: "Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors", ONCOGENE, vol. 22, no. 18, 8 May 2003 (2003-05-08), pages 2812 - 2822, XP002546490 * |
| BRIEL D; DRESCHER S; DOBNER B: "Selective nucleophilic replacement of the benzylsulfanyl group in 2,4-disulfanyl-substituted thieno[2,3-d]pyrimidin-6-carboxylic acid derivatives by secondary amines", JOURNAL OF HETEROCYCLIC CHEMISTRY, vol. 42, no. 5, July 2005 (2005-07-01), pages 841 - 846, XP002504098 * |
| HAYAKAWA M, KAIZAWA H, MORITOMO H, KOIZUMI T, OHISHI T, YAMANO M, OKADA M, OHTA M, TSUKAMOTO S, RAYNAUD F I ET AL.: "Synthesis and biological evaluation of pyrido[3',2':4,5]furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110alpha inhibitors", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 17, no. 9, 3 April 2007 (2007-04-03), XP022015320 * |
| LI TIANHONG; LING YI-HE; GOLDMAN I DAVID; PEREZ-SOLER ROMAN: "Schedule-dependent cytotoxic synergism of pemetrexed and erlotinib in human non-small cell lung cancer cells", CANCER RESEARCH, vol. 13, no. 11, 1 June 2007 (2007-06-01), pages 3413 - 3422, XP002546488 * |
| LOPREVITE MAURA ET AL: "In vitro study of farnesyltransferase inhibitor SCH 66336, in combination with chemotherapy and radiation, in non-small cell lung cancer cell lines", ONCOLOGY REPORTS, NATIONAL HELLENIC RESEARCH FOUNDATION, ATHENS, GR, vol. 11, no. 2, 1 February 2004 (2004-02-01), pages 407 - 414, XP009091362, ISSN: 1021-335X * |
| MENDOZA NERISSA; PHILLIPS GAIL LEWIS; SILVA JOHNNY; SCHWALL RALPH; WICKRAMASINGHE DINELI: "Inhibition of ligand-mediated HER2 activation in androgen-independent prostate cancer", CANCER RESEARCH, vol. 62, no. 19, 1 October 2002 (2002-10-01), pages 5485 - 5488, XP002546487 * |
| NIELSEN L L ET AL: "COMBINATION THERAPY WITH THE FARNESYL PROTEIN TRANSFERASE INHIBITORSCH66336 AND SCH58500 (P53 ADENOVIRUS) IN PRECLINICAL CANCER MODELS", CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, BALTIMORE, MD., US, vol. 59, no. 23, 1 December 1999 (1999-12-01), pages 5896 - 5901, XP000919397, ISSN: 0008-5472 * |
| TUMKEVICIUS S ET AL: "First Example of Synthesis of Thieno[2,3-d]pyrimidine-6-carbaldehydes by Oxidation of Thieno[2,3-d]pyrimidin-6-yl Methanols with Molecular Iodine", CHEMISTRY OF HETEROCYCLIC COMPOUNDS, KLUWER ACADEMIC PUBLISHERS-CONSULTANTS BUREAU, NE, vol. 41, no. 6, 1 June 2005 (2005-06-01), pages 800 - 801, XP019276371, ISSN: 1573-8353 * |
| YU DIHUA; HUNG MIEN-CHIE: "Role of erbB2 in breast cancer chemosensitivity", BIOESSAYS, vol. 22, no. 7, July 2000 (2000-07-01), pages 673 - 680, XP002546485 * |
| ZHOU H ET AL: "Effects of the EGFR/HER2 kinase inhibitor GW572016 on EGFR- and her2-overexpressing breast cancer cell line proliferation,radiosensit ization, and resistance", INTERNATIONAL JOURNAL OF RADIATION: ONCOLOGY BIOLOGY PHYSICS, PERGAMON PRESS, US, vol. 58, no. 2, 1 February 2004 (2004-02-01), pages 344 - 352, XP002996475, ISSN: 0360-3016 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11529350B2 (en) | 2019-07-03 | 2022-12-20 | Sumitomo Pharma Oncology, Inc. | Tyrosine kinase non-receptor 1 (TNK1) inhibitors and uses thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| IL204333A (en) | 2016-08-31 |
| PE20090678A1 (en) | 2009-06-27 |
| JP5658565B2 (en) | 2015-01-28 |
| TWI471134B (en) | 2015-02-01 |
| EP2205242A2 (en) | 2010-07-14 |
| CN101939006B (en) | 2015-09-16 |
| RU2523890C2 (en) | 2014-07-27 |
| AU2008298948B2 (en) | 2014-09-04 |
| ZA201002475B (en) | 2011-06-29 |
| KR20100085912A (en) | 2010-07-29 |
| RU2010112837A (en) | 2011-10-20 |
| EP2205242B1 (en) | 2015-04-15 |
| US20110223619A1 (en) | 2011-09-15 |
| BRPI0816769A2 (en) | 2016-11-29 |
| US8604014B2 (en) | 2013-12-10 |
| MX2010002543A (en) | 2010-03-29 |
| HK1145287A1 (en) | 2011-04-15 |
| AR068402A1 (en) | 2009-11-18 |
| CA2699202A1 (en) | 2009-03-19 |
| KR101584823B1 (en) | 2016-01-22 |
| CA2699202C (en) | 2016-09-27 |
| CN101939006A (en) | 2011-01-05 |
| US20090098135A1 (en) | 2009-04-16 |
| ES2537352T3 (en) | 2015-06-05 |
| TW200920377A (en) | 2009-05-16 |
| JP2010539177A (en) | 2010-12-16 |
| AU2008298948A1 (en) | 2009-03-19 |
| US20130345217A1 (en) | 2013-12-26 |
| WO2009036082A2 (en) | 2009-03-19 |
| US8247397B2 (en) | 2012-08-21 |
| CL2008002687A1 (en) | 2009-01-16 |
| PE20140100A1 (en) | 2014-02-12 |
| MX338504B (en) | 2016-04-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2009036082A3 (en) | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use | |
| TW200801012A (en) | Phosphoinositide 3-kinase inhibitor compounds and methods of use | |
| WO2010105008A3 (en) | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents for the treatment of hematopoietic malignancies | |
| WO2007127175A3 (en) | Pharmaceutical compounds | |
| WO2009111278A3 (en) | Raf inhibitor compounds and methods of use thereof | |
| WO2008073785A3 (en) | Phosphoinositide 3-kinase inhibitor compounds and methods of use | |
| WO2007027855A3 (en) | Raf inhibitor compounds and methods of use thereof | |
| MX2009005950A (en) | Phosphoinositide 3-kinase inhibitor compounds and methods of use. | |
| MX2010010659A (en) | Benzopyran and benzoxepin pi3k inhibitor compounds and methods of use. | |
| WO2007146824A3 (en) | Quinoline compounds and methods of use | |
| WO2006125101A3 (en) | Raf inhibitor compounds and methods of use thereof | |
| MX340013B (en) | Benzoxazepin compounds selective for pi3k p110 delta and methods of use. | |
| MX2011012520A (en) | Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use. | |
| WO2011025938A3 (en) | Raf inhibitor compounds and methods of use thereof | |
| SG10201407781SA (en) | Benzoxepin PI3K Inhibitor Compounds And Methods Of Use | |
| PH12013501779A1 (en) | Pyrrolopyridines as kinase inhibitors | |
| WO2007103308A3 (en) | Heterobicyclic pyrazole compounds and methods of use | |
| WO2008028141A3 (en) | Raf inhibitor compounds and methods of use thereof | |
| AU2009312464A8 (en) | Triazine, pyrimidine and pyridine analogs and their use as therapeutic agents and diagnostic probes | |
| WO2009151598A8 (en) | Diazacarbazoles and methods of use | |
| SG178900A1 (en) | Raf inhibitor compounds and methods of use thereof | |
| WO2007109251A3 (en) | Tumor necrosis factor alpha inhibitors and their use in the treatment of human diseases | |
| MX2014014828A (en) | 5-azaindazole compounds and methods of use. | |
| MX2014001239A (en) | PYRAZOLO[3,4-c]PYRIDINE COMPOUNDS AND METHODS OF USE. | |
| MX349550B (en) | 1, 7 - diazacarbazoles and their use in the treatment of cancer. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| WWE | Wipo information: entry into national phase |
Ref document number: 200880116412.4 Country of ref document: CN |
|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08799418 Country of ref document: EP Kind code of ref document: A2 |
|
| WWE | Wipo information: entry into national phase |
Ref document number: MX/A/2010/002543 Country of ref document: MX |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 204333 Country of ref document: IL |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2699202 Country of ref document: CA |
|
| ENP | Entry into the national phase |
Ref document number: 2010524965 Country of ref document: JP Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2008298948 Country of ref document: AU |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2390/DELNP/2010 Country of ref document: IN |
|
| ENP | Entry into the national phase |
Ref document number: 20107007940 Country of ref document: KR Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2010112837 Country of ref document: RU Ref document number: 2008799418 Country of ref document: EP |
|
| ENP | Entry into the national phase |
Ref document number: 2008298948 Country of ref document: AU Date of ref document: 20080910 Kind code of ref document: A |
|
| REG | Reference to national code |
Ref country code: BR Ref legal event code: B01E Ref document number: PI0816769 Country of ref document: BR Free format text: APRESENTE DOCUMENTOS COMPROBATORIOS QUE EXPLIQUEM A DIVERGENCIA NO NOME DE UM DOS INVENTORES QUE CONSTA NA PUBLICACAO INTERNACIONAL WO/2009/036082 DE 19/03/2009 ULKA VIJAPURKAR E O CONSTANTE DA PETICAO INICIAL NO 020100022056 DE 12/03/2010 "ULKA VJAPURKAR . |
|
| ENP | Entry into the national phase |
Ref document number: PI0816769 Country of ref document: BR Kind code of ref document: A2 Effective date: 20100312 |