PL4058151T3 - Nowa sól związku terfenylowego - Google Patents
Nowa sól związku terfenylowegoInfo
- Publication number
- PL4058151T3 PL4058151T3 PL20886261.5T PL20886261T PL4058151T3 PL 4058151 T3 PL4058151 T3 PL 4058151T3 PL 20886261 T PL20886261 T PL 20886261T PL 4058151 T3 PL4058151 T3 PL 4058151T3
- Authority
- PL
- Poland
- Prior art keywords
- novel salt
- terphenyl compound
- terphenyl
- compound
- salt
- Prior art date
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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/203—Retinoic acids ; Salts thereof
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/04—Monocyclic monocarboxylic acids
- C07C63/06—Benzoic acid
- C07C63/08—Salts thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962934923P | 2019-11-13 | 2019-11-13 | |
| PCT/JP2020/042383 WO2021095835A1 (en) | 2019-11-13 | 2020-11-13 | Novel salt of terphenyl compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL4058151T3 true PL4058151T3 (pl) | 2025-08-04 |
Family
ID=75912767
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL20886261.5T PL4058151T3 (pl) | 2019-11-13 | 2020-11-13 | Nowa sól związku terfenylowego |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US12419858B2 (pl) |
| EP (2) | EP4058018A4 (pl) |
| JP (2) | JP7379680B2 (pl) |
| KR (2) | KR20220113390A (pl) |
| CN (2) | CN114828844A (pl) |
| AU (2) | AU2020382214B2 (pl) |
| BR (2) | BR112022009221A2 (pl) |
| CA (2) | CA3157404A1 (pl) |
| DK (1) | DK4058151T3 (pl) |
| ES (1) | ES3034158T3 (pl) |
| FI (1) | FI4058151T3 (pl) |
| HU (1) | HUE072206T2 (pl) |
| MX (2) | MX2022005812A (pl) |
| PH (2) | PH12022551169A1 (pl) |
| PL (1) | PL4058151T3 (pl) |
| PT (1) | PT4058151T (pl) |
| TW (2) | TWI874490B (pl) |
| WO (2) | WO2021095835A1 (pl) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12435128B2 (en) | 2017-05-31 | 2025-10-07 | Taiho Pharmaceutical Co., Ltd. | Method for predicting therapeutic effect of LSD1 inhibitor based on expression of INSM1 |
| PH12022551169A1 (en) | 2019-11-13 | 2024-02-19 | Astex Pharmaceuticals Inc | METHODS OF TREATING LSD1-RELATED DISEASES and Disorders WITH LSD1 INHIBITORS |
| BR112023020554A2 (pt) | 2021-04-08 | 2023-12-05 | Oryzon Genomics Sa | Combinações de inibidores de lsd1 para o tratamento de cânceres mieloides |
| WO2022240886A1 (en) * | 2021-05-11 | 2022-11-17 | Astex Pharmaceuticals, Inc. | Solid forms of salts of 4-[5-[(3s)-3-aminopyrrolidine-1-carbonyl]-2-[2-fluoro-4-(2-hydroxy-2-ethylpropyl)phenyl]phenyl]-2-fluoro-benzonitrile |
| KR20240065302A (ko) * | 2021-09-30 | 2024-05-14 | 다이호야쿠힌고교 가부시키가이샤 | 비페닐 화합물 및 면역 체크포인트 분자 조절제를 사용한 암에 대한 조합 요법 |
| CN118510763A (zh) * | 2021-10-26 | 2024-08-16 | 阿斯泰克斯制药公司 | 1-(3-氨基吡咯烷-1-羰基)-3,4-二苯基苯化合物的苯甲酸盐的制备方法 |
| US20250295660A1 (en) | 2022-05-09 | 2025-09-25 | Oryzon Genomics, S.A. | Methods of treating nf1-mutant tumors using lsd1 inhibitors |
| JP2025516647A (ja) | 2022-05-09 | 2025-05-30 | オリゾン・ゲノミクス・ソシエダッド・アノニマ | Ｌｓｄ１阻害薬を用いる悪性末梢神経鞘腫（ｍｐｎｓｔ）の治療法 |
| AU2023385514A1 (en) | 2022-11-24 | 2025-07-10 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors and menin inhibitors for treating cancer |
| WO2024229073A1 (en) * | 2023-05-02 | 2024-11-07 | Otsuka Pharmaceutical Co., Ltd. | Response-based dosing for treating cancer with a hypomethylating agent and cedazuridine |
| WO2024229406A1 (en) | 2023-05-04 | 2024-11-07 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| WO2025034702A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Rmc-6291 for use in the treatment of ras protein-related disease or disorder |
| TW202530228A (zh) | 2023-10-12 | 2025-08-01 | 美商銳新醫藥公司 | Ｒａｓ抑制劑 |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE8801518D0 (sv) * | 1988-04-22 | 1988-04-22 | Astra Pharma Prod | A novel process |
| US6225049B1 (en) | 1992-06-17 | 2001-05-01 | The United States Of America As Represented By The Department Of Health And Human Services | Human insulinoma-associated cDNA |
| JP2005516938A (ja) | 2001-12-13 | 2005-06-09 | ナトロジェン・セラピューティクス・インコーポレーテッド | イソインジゴ、インジゴおよびインジルビンの誘導体、ならびに癌治療における使用 |
| EP1537878B1 (en) | 2002-07-03 | 2010-09-22 | Ono Pharmaceutical Co., Ltd. | Immunopotentiating compositions |
| EP1792622A1 (en) | 2005-11-11 | 2007-06-06 | GPC Biotech AG | Anti-proliferative combination therapy comprising a platinum-based chemotherapeutic agent and EGFR inhibitors or pyrimidine analogues |
| US8455477B2 (en) | 2008-08-05 | 2013-06-04 | Merck Sharp & Dohme Corp. | Therapeutic compounds |
| US8163509B2 (en) | 2008-10-20 | 2012-04-24 | The Regents Of The University Of Colorado, A Body Corporate | Biological markers predictive of anti-cancer response to insulin-like growth factor-1 receptor kinase inhibitors |
| US8367679B2 (en) | 2008-12-09 | 2013-02-05 | Merck Sharp & Dohme Corp. | Biaryl carboxamides |
| JP2012524280A (ja) | 2009-04-17 | 2012-10-11 | オーエスアイ・ファーマシューティカルズ，エルエルシー | 上皮成長因子受容体キナーゼ阻害剤に対する抗がん反応を予測するための生物学的マーカー |
| BR112012027062B8 (pt) | 2010-04-20 | 2021-05-25 | Fond Ieo | composto, processo para a preparação de um composto e usos do mesmo |
| ME03085B (me) | 2010-07-29 | 2019-01-20 | Oryzon Genomics Sa | Demetilaza inhibitori lsd1 zasnovani na arilciklopropilaminu i njihova medicinska primjena |
| US9345767B2 (en) | 2011-05-16 | 2016-05-24 | Taiho Pharmaceutical Co., Ltd. | Method for selecting chemotherapy for gastric cancer patient using combination drug of tegafur, gimeracil and oteracil potassium and EGFR inhibitor |
| BR112014009306B1 (pt) | 2011-10-20 | 2021-07-20 | Oryzon Genomics S.A. | Compostos de (hetero)aril ciclopropilamina como inibidores de lsd1 |
| US9271999B2 (en) * | 2012-05-09 | 2016-03-01 | Cantex Pharmaceuticals, Inc. | Treatment of myelosuppression |
| US9834521B2 (en) | 2013-03-15 | 2017-12-05 | Ariad Pharmaceuticals, Inc. | Choline kinase inhibitors |
| MX383590B (es) | 2013-08-06 | 2025-03-11 | Imago Biosciences Inc | Inhibidores de kdm1a para el tratamiento de enfermedades. |
| US9266907B2 (en) | 2013-09-05 | 2016-02-23 | King Abdullah University Of Science And Technology | Tunable rare-earth fcu-metal-organic frameworks |
| LT3080100T (lt) | 2013-12-11 | 2023-02-27 | Celgene Quanticel Research, Inc. | Lizinui specifinės demetilazės-1 inhibitoriai |
| AU2014374043B2 (en) | 2014-01-06 | 2019-06-27 | Algomedix, Inc. | TRPA1 modulators |
| US9255097B2 (en) | 2014-05-01 | 2016-02-09 | Quanticel Pharmaceuticals, Inc. | Inhibitors of lysine specific demethylase-1 |
| WO2016007727A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| JP2017528452A (ja) | 2014-08-25 | 2017-09-28 | ユニバーシティ・オブ・キャンベラＵｎｉｖｅｒｓｉｔｙ ｏｆ Ｃａｎｂｅｒｒａ | がん幹細胞を調節するための組成物およびその使用 |
| CN107074787B (zh) | 2014-09-05 | 2020-10-27 | 赛尔基因昆蒂赛尔研究公司 | 赖氨酸特异性脱甲基酶-1的抑制剂 |
| KR102891799B1 (ko) | 2015-04-20 | 2025-11-26 | 이펙터 테라퓨틱스, 인크. | 암 및 감염 치료에 사용하기 위한 면역 체크포인트 조절 인자의 억제제 |
| WO2017013061A1 (en) | 2015-07-17 | 2017-01-26 | Oryzon Genomics, S.A. | Biomarkers associated with lsd1 inhibitors and uses thereof |
| PL3381896T3 (pl) * | 2015-11-27 | 2023-05-08 | Taiho Pharmaceutical Co., Ltd. | Związek bifenylowy lub jego sól |
| WO2018136961A1 (en) | 2017-01-23 | 2018-07-26 | Syros Pharmaceuticals Inc. | METHODS OF TREATING PATIENTS WITH A RETINOIC ACID RECEPTOR-α AGONIST AND AN ANTI-CD38 ANTIBODY |
| MX391414B (es) | 2017-05-26 | 2025-03-21 | Taiho Pharmaceutical Co Ltd | Compuesto novedoso de bifenilo o sal del mismo. |
| WO2018216795A1 (ja) * | 2017-05-26 | 2018-11-29 | 大鵬薬品工業株式会社 | 新規なビフェニル化合物を用いた抗腫瘍効果増強剤 |
| US12435128B2 (en) | 2017-05-31 | 2025-10-07 | Taiho Pharmaceutical Co., Ltd. | Method for predicting therapeutic effect of LSD1 inhibitor based on expression of INSM1 |
| CA3068591A1 (en) | 2017-06-30 | 2019-01-03 | Celgene Corporation | Compositions and methods of use of 2-(4-chlorophenyl)-n-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl) methyl)-2,2-difluoroacetamide |
| WO2019075327A1 (en) | 2017-10-12 | 2019-04-18 | Dana-Farber Cancer Institute, Inc. | TREATMENT OF MERKEL CELL CARCINOMA |
| WO2019083971A1 (en) | 2017-10-23 | 2019-05-02 | Children's Medical Center Corporation | METHODS OF TREATING CANCER USING LSD1 INHIBITORS IN COMBINATION WITH IMMUNOTHERAPY |
| CA3083373A1 (en) | 2017-11-29 | 2019-06-06 | Epiaxis Therapeutics Pty Ltd | Enhancing t-cell function and treating a t-cell dysfunctional disorder with a combination of an lsd inhibitor and a pd1 binding antagonist |
| WO2019136016A1 (en) | 2018-01-02 | 2019-07-11 | Celgene Corporation | Isotopologues of 2-(4-chlorophenyl)-n-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)methyl)-2,2-difluoroacetamide |
| US20220289705A1 (en) | 2019-07-17 | 2022-09-15 | Summit (Oxford) Limited | Process for the preparation of ridinilazole and crystalline forms thereof |
| PH12022551169A1 (en) | 2019-11-13 | 2024-02-19 | Astex Pharmaceuticals Inc | METHODS OF TREATING LSD1-RELATED DISEASES and Disorders WITH LSD1 INHIBITORS |
| WO2021178807A1 (en) | 2020-03-06 | 2021-09-10 | Celgene Quanticel Research, Inc. | Combination of an lsd-1 inhibitor and nivolumab for use in treating sclc or sqnsclc |
-
2020
- 2020-11-13 PH PH1/2022/551169A patent/PH12022551169A1/en unknown
- 2020-11-13 BR BR112022009221A patent/BR112022009221A2/pt unknown
- 2020-11-13 CN CN202080079021.0A patent/CN114828844A/zh active Pending
- 2020-11-13 KR KR1020227019783A patent/KR20220113390A/ko active Pending
- 2020-11-13 EP EP20886658.2A patent/EP4058018A4/en active Pending
- 2020-11-13 JP JP2022519478A patent/JP7379680B2/ja active Active
- 2020-11-13 PT PT208862615T patent/PT4058151T/pt unknown
- 2020-11-13 US US17/775,795 patent/US12419858B2/en active Active
- 2020-11-13 MX MX2022005812A patent/MX2022005812A/es unknown
- 2020-11-13 CN CN202080078991.9A patent/CN114728899B/zh active Active
- 2020-11-13 HU HUE20886261A patent/HUE072206T2/hu unknown
- 2020-11-13 ES ES20886261T patent/ES3034158T3/es active Active
- 2020-11-13 PL PL20886261.5T patent/PL4058151T3/pl unknown
- 2020-11-13 KR KR1020227019781A patent/KR102825246B1/ko active Active
- 2020-11-13 EP EP20886261.5A patent/EP4058151B1/en active Active
- 2020-11-13 PH PH1/2022/551137A patent/PH12022551137A1/en unknown
- 2020-11-13 AU AU2020382214A patent/AU2020382214B2/en active Active
- 2020-11-13 JP JP2022527859A patent/JP7492002B2/ja active Active
- 2020-11-13 BR BR112022008020A patent/BR112022008020A2/pt unknown
- 2020-11-13 CA CA3157404A patent/CA3157404A1/en active Pending
- 2020-11-13 CA CA3158442A patent/CA3158442A1/en active Pending
- 2020-11-13 TW TW109139813A patent/TWI874490B/zh active
- 2020-11-13 DK DK20886261.5T patent/DK4058151T3/da active
- 2020-11-13 FI FIEP20886261.5T patent/FI4058151T3/fi active
- 2020-11-13 TW TW109139799A patent/TWI874489B/zh active
- 2020-11-13 US US17/775,800 patent/US20220387384A1/en active Pending
- 2020-11-13 MX MX2022005811A patent/MX2022005811A/es unknown
- 2020-11-13 WO PCT/JP2020/042383 patent/WO2021095835A1/en not_active Ceased
- 2020-11-13 WO PCT/JP2020/042410 patent/WO2021095840A1/en not_active Ceased
- 2020-11-13 AU AU2020382379A patent/AU2020382379B2/en active Active
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