CY1124068T1 - Στερεες μορφες ενος εκλεκτικου αναστολεα cdk4/6 - Google Patents
Στερεες μορφες ενος εκλεκτικου αναστολεα cdk4/6Info
- Publication number
- CY1124068T1 CY1124068T1 CY20211100336T CY211100336T CY1124068T1 CY 1124068 T1 CY1124068 T1 CY 1124068T1 CY 20211100336 T CY20211100336 T CY 20211100336T CY 211100336 T CY211100336 T CY 211100336T CY 1124068 T1 CY1124068 T1 CY 1124068T1
- Authority
- CY
- Cyprus
- Prior art keywords
- inhibitor
- solid forms
- selective cdk4
- dosage forms
- free base
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Η παρούσα εφεύρεση αναφέρεται στην κρυσταλλική ελεύθερη βάση της 6-ακετυλ-8-κυκλοπεντυλ-5-μεθυλ-2-(5-πιπεραζιν-1-υλ-πυριδιν-2-υλαμινο)-8Η-πυριδο[2,3-d-]πυριμιδιν-7-όνης (τύπος (Ι)) που έχει βελτιωμένες ιδιότητες, σε φαρμακευτικές συνθέσεις και μορφές δόσεως που περιλαμβάνουν την ελεύθερη βάση και σε μεθόδους για τη δημιουργία και τη χρήση αυτών των ενώσεων, συνθέσεων και μορφών δόσεως στην αγωγή νόσων υπερπλασίας των κυττάρων, όπως ο καρκίνος.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361767761P | 2013-02-21 | 2013-02-21 | |
| EP14705884.6A EP2958916B1 (en) | 2013-02-21 | 2014-02-08 | Solid forms of a selective cdk4/6 inhibitor |
| PCT/IB2014/058865 WO2014128588A1 (en) | 2013-02-21 | 2014-02-08 | Solid forms of a selective cdk4/6 inhibitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1124068T1 true CY1124068T1 (el) | 2022-05-27 |
Family
ID=50151343
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY181101034T CY1120734T1 (el) | 2013-02-21 | 2018-10-05 | Στερεες μορφες ενος εκλεκτικου αναστολεα cdk4/6 |
| CY20211100336T CY1124068T1 (el) | 2013-02-21 | 2021-04-16 | Στερεες μορφες ενος εκλεκτικου αναστολεα cdk4/6 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY181101034T CY1120734T1 (el) | 2013-02-21 | 2018-10-05 | Στερεες μορφες ενος εκλεκτικου αναστολεα cdk4/6 |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US20160002223A1 (el) |
| EP (2) | EP3431475B1 (el) |
| JP (3) | JP6381016B2 (el) |
| KR (2) | KR20150107872A (el) |
| CN (3) | CN107759594A (el) |
| AR (1) | AR094842A1 (el) |
| AU (1) | AU2014220354B2 (el) |
| BR (1) | BR112015019508A8 (el) |
| CA (1) | CA2900322C (el) |
| CY (2) | CY1120734T1 (el) |
| DK (2) | DK3431475T3 (el) |
| ES (2) | ES2869277T3 (el) |
| HK (2) | HK1211032A1 (el) |
| HU (2) | HUE040434T2 (el) |
| IL (1) | IL240277B (el) |
| MX (2) | MX363715B (el) |
| PL (2) | PL2958916T3 (el) |
| PT (2) | PT3431475T (el) |
| RU (1) | RU2619944C2 (el) |
| SG (1) | SG11201505680RA (el) |
| SI (2) | SI2958916T1 (el) |
| TR (1) | TR201816077T4 (el) |
| TW (2) | TWI670269B (el) |
| WO (1) | WO2014128588A1 (el) |
Families Citing this family (108)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2679130C2 (ru) | 2012-07-11 | 2019-02-06 | Блюпринт Медсинс Корпорейшн | Ингибиторы рецептора фактора роста фибробластов |
| EP3431475B1 (en) | 2013-02-21 | 2021-04-07 | Pfizer Inc | Solid forms of a selective cdk4/6 inhibitor |
| EP3060560A1 (en) | 2013-10-25 | 2016-08-31 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| US9695165B2 (en) | 2014-01-15 | 2017-07-04 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| EP3180007A1 (en) * | 2014-08-14 | 2017-06-21 | Sun Pharmaceutical Industries Ltd | Crystalline forms of palbociclib |
| WO2016030439A1 (en) * | 2014-08-28 | 2016-03-03 | Ratiopharm Gmbh | Method of producing palbociclib and pharmaceutical compositions comprising the same |
| CN105616418A (zh) * | 2014-11-07 | 2016-06-01 | 江苏豪森药业集团有限公司 | 含有细胞周期蛋白抑制剂的药物制剂及其制备方法 |
| WO2016090257A1 (en) * | 2014-12-05 | 2016-06-09 | Crystal Pharmatech Inc. | Salts and crystalline forms of 6-acetyl-8-cyclopentyl-5-methyl-2((5-(piperazin-1-yl)pyridin-2-yl)amino)pyrido[2,3-d] pyrimidin-7(8h)-one (palbociclib) |
| WO2016092442A1 (en) * | 2014-12-08 | 2016-06-16 | Sun Pharmaceutical Industries Limited | Processes for the preparation of crystalline forms of palbociclib acetate |
| CN104610254B (zh) * | 2015-01-26 | 2017-02-01 | 新发药业有限公司 | 一种帕博赛布的低成本制备方法 |
| CZ201589A3 (cs) | 2015-02-11 | 2016-08-24 | Zentiva, K.S. | Pevné formy soli Palbociclibu |
| WO2016156070A1 (en) | 2015-04-02 | 2016-10-06 | Sandoz Ag | Modified particles of palbociclib |
| EP3078663A1 (en) | 2015-04-09 | 2016-10-12 | Sandoz Ag | Modified particles of palbociclib |
| CN106117199A (zh) * | 2015-05-04 | 2016-11-16 | 江苏恒瑞医药股份有限公司 | 一种细胞周期蛋白依赖性激酶抑制剂的二羟乙基磺酸盐、其结晶形式及其制备方法 |
| RU2686840C1 (ru) * | 2015-06-04 | 2019-05-06 | Пфайзер Инк. | Твёрдые лекарственные формы палбоциклиба |
| CN106317053A (zh) * | 2015-06-29 | 2017-01-11 | 北大方正集团有限公司 | 一种帕博昔布晶型a的制备方法 |
| CN106397431A (zh) * | 2015-07-28 | 2017-02-15 | 苏州国匡医药科技有限公司 | 一种抗肿瘤药物的新晶型及其制备方法和用途 |
| CN105153149B (zh) * | 2015-07-29 | 2017-09-19 | 江苏中邦制药有限公司 | 一种选择性激酶抑制剂Palbociclib的制备方法 |
| WO2017021111A1 (en) * | 2015-08-05 | 2017-02-09 | Ratiopharm Gmbh | New crystalline form and acetic acid adducts of palbociclib |
| CN105085517B (zh) * | 2015-08-06 | 2016-11-23 | 天津华洛康生物科技有限公司 | 一种结晶型帕博西尼游离碱水合物及其制备方法 |
| US11780848B2 (en) | 2015-10-16 | 2023-10-10 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1- carboxamide and solid state forms thereof |
| US12365689B2 (en) | 2015-10-16 | 2025-07-22 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US11365198B2 (en) | 2015-10-16 | 2022-06-21 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| CN120289468A (zh) | 2015-10-16 | 2025-07-11 | 艾伯维公司 | 制备咪唑并[1,2-a]吡咯并[2,3-e]吡嗪类化合物及其固态形式的方法 |
| US10550126B2 (en) | 2015-10-16 | 2020-02-04 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| CN106608876B (zh) * | 2015-10-21 | 2018-06-19 | 新发药业有限公司 | 一种高纯度帕博西尼的制备方法 |
| HU230962B1 (hu) | 2015-10-28 | 2019-06-28 | Egis Gyógyszergyár Zrt. | Palbociclib sók |
| CN106632311B (zh) * | 2015-11-02 | 2021-05-18 | 上海科胜药物研发有限公司 | 一种帕博西尼晶型a和晶型b的制备方法 |
| CN106831759A (zh) * | 2015-12-03 | 2017-06-13 | 上海星泰医药科技有限公司 | 帕布昔利布及其中间体的制备方法 |
| CN105541832A (zh) * | 2015-12-15 | 2016-05-04 | 南京艾德凯腾生物医药有限责任公司 | 一种羟乙基磺酸盐帕布昔利布的制备方法 |
| WO2017115315A1 (en) * | 2015-12-30 | 2017-07-06 | Dr. Reddy's Laboratories Limited | Solid forms of palbociclib |
| CN105524059A (zh) * | 2016-01-06 | 2016-04-27 | 北京修正创新药物研究院有限公司 | 一种帕波西比杂质的制备方法 |
| WO2017130219A1 (en) | 2016-01-25 | 2017-08-03 | Mylan Laboratories Limited | Amorphous solid dispersion of palbociclib |
| GB201601329D0 (en) | 2016-01-25 | 2016-03-09 | Mohammad Mohammad A | Inverse gas chromatography standard solutions, device and method |
| WO2017145054A1 (en) | 2016-02-24 | 2017-08-31 | Lupin Limited | Modified particles of crystalline palbociclib free base and process for the preparation thereof |
| US10449195B2 (en) | 2016-03-29 | 2019-10-22 | Shenzhen Pharmacin Co., Ltd. | Pharmaceutical formulation of palbociclib and a preparation method thereof |
| CN106336411B (zh) * | 2016-04-27 | 2018-03-06 | 上海医药集团股份有限公司 | Cdk4/6抑制剂帕博西尼高纯度原料药的制备工艺及用途 |
| WO2017197904A2 (zh) * | 2016-05-08 | 2017-11-23 | 上海诚妙医药科技有限公司 | 帕布昔利布的新晶型及其制备方法及其用途 |
| CN105924439B (zh) * | 2016-06-24 | 2017-11-24 | 石家庄海瑞药物科技有限公司 | 一种帕布昔利布的制备方法 |
| CN106146494B (zh) * | 2016-06-29 | 2018-02-06 | 重庆华邦制药有限公司 | 用于制备帕布昔利布a型晶的溶剂及制备方法 |
| EP3481825A1 (en) | 2016-07-07 | 2019-05-15 | Plantex Ltd. | Solid state forms of palbociclib dimesylate |
| CN106220627A (zh) * | 2016-07-31 | 2016-12-14 | 合肥远志医药科技开发有限公司 | 一种高纯度帕布昔利布的工业化制备方法 |
| CN106220626A (zh) * | 2016-07-31 | 2016-12-14 | 合肥远志医药科技开发有限公司 | 一种帕布昔利布的多晶型及其制备方法 |
| MA45920B1 (fr) | 2016-08-15 | 2021-08-31 | Pfizer | Inhibiteurs de pyridopyrimidinone cdk2/4/6 |
| WO2018049233A1 (en) | 2016-09-08 | 2018-03-15 | Nicolas Stransky | Inhibitors of the fibroblast growth factor receptor in combination with cyclin-dependent kinase inhibitors |
| WO2018065999A1 (en) | 2016-10-07 | 2018-04-12 | Mylan Laboratories Limited | Novel polymorph of an intermediate for palbociclib synthesis |
| WO2018073574A1 (en) | 2016-10-20 | 2018-04-26 | Cipla Limited | Polymorphic forms of palbociclib |
| BR112019005526A2 (pt) | 2016-10-20 | 2019-06-18 | Pfizer | agentes antiproliferativos para tratamento de pah |
| CN108017630B (zh) * | 2016-10-31 | 2022-10-11 | 上海创诺制药有限公司 | 一种小比表面积帕博西尼游离碱的制备方法 |
| US20190275049A1 (en) | 2016-11-16 | 2019-09-12 | Pfizer Inc. | Combination of an EGFR T790M Inhibitor and a CDK Inhibitor for the Treatment of Non-Small Cell Lung Cancer |
| CN108117550B (zh) * | 2016-11-29 | 2020-08-14 | 上海医药工业研究院 | 吡啶并[2,3-d]嘧啶类化合物的制备方法 |
| IL267299B (en) | 2016-12-16 | 2022-09-01 | Cstone Pharmaceuticals | Cdk4/6 inhibitor |
| US20200054560A1 (en) * | 2017-04-21 | 2020-02-20 | Alnova Pharmaceuticals, Ltd. | Palbociclib compositions and methods thereof |
| CN108864078B (zh) * | 2017-05-10 | 2021-10-15 | 江苏豪森药业集团有限公司 | 帕博西尼晶型b的制备方法 |
| WO2019014398A1 (en) | 2017-07-11 | 2019-01-17 | Actym Therapeutics, Inc. | MODIFIED IMMUNOSTIMULATORY BACTERIAL STRAINS AND USES THEREOF |
| EA202090402A1 (ru) | 2017-07-28 | 2020-05-19 | Синтон Б.В. | Фармацевтическая композиция, содержащая пальбоциклиб |
| JP7250764B2 (ja) | 2017-08-18 | 2023-04-03 | コセラ バイオサイエンス, インコーポレイテッド | Tg02の多形形態 |
| KR20200057705A (ko) | 2017-10-27 | 2020-05-26 | 프레세니어스 카비 온콜로지 리미티드 | 리보시클립 및 그의 염의 제조를 위한 개선된 방법 |
| CN109897034A (zh) * | 2017-12-07 | 2019-06-18 | 南京卡文迪许生物工程技术有限公司 | 一种高纯度晶型a帕布昔利布及其制备方法和药物组合物 |
| KR20200108867A (ko) | 2018-01-08 | 2020-09-21 | 쥐원 쎄라퓨틱스, 인크. | G1t38 우수한 투여 요법 |
| CN108586452A (zh) * | 2018-01-12 | 2018-09-28 | 重庆市碚圣医药科技股份有限公司 | 一种帕博西尼中间体的合成方法 |
| JP2021514975A (ja) | 2018-02-27 | 2021-06-17 | ファイザー・インク | サイクリン依存性キナーゼ阻害剤およびbet−ブロモドメイン阻害剤の組合せ |
| CN108299422B (zh) * | 2018-02-28 | 2019-10-25 | 杭州福斯特药业有限公司 | 一种帕泊昔利布中间体的制备方法 |
| EP4309656A3 (en) | 2018-05-14 | 2024-02-28 | Pfizer Inc. | Oral solution formulation |
| CN108558745A (zh) * | 2018-05-17 | 2018-09-21 | 苏州莱克施德药业有限公司 | 一种帕博西林中间体的合成方法 |
| SI3802529T1 (sl) | 2018-05-24 | 2024-03-29 | Synthon B.V. | Postopek za izdelavo palbocikliba |
| WO2019238088A1 (zh) * | 2018-06-13 | 2019-12-19 | 基石药业 | 吡啶并吡啶酮衍生物的盐型及晶型 |
| US11242528B2 (en) | 2018-08-28 | 2022-02-08 | Actym Therapeutics, Inc. | Engineered immunostimulatory bacterial strains and uses thereof |
| JP6952747B2 (ja) | 2018-09-18 | 2021-10-20 | ファイザー・インク | がん処置のためのTGFβ阻害剤およびCDK阻害剤の組合せ |
| KR20210102211A (ko) | 2018-10-24 | 2021-08-19 | 이펙터 테라퓨틱스, 인크. | Mnk 억제제의 결정질 형태 |
| CN109336886A (zh) * | 2018-12-07 | 2019-02-15 | 重庆三圣实业股份有限公司 | 一种帕博西尼的制备方法及其产品 |
| WO2020148635A1 (en) * | 2019-01-17 | 2020-07-23 | Pfizer Inc. | Crystalline form of a cdk inhibitor |
| WO2020157709A1 (en) | 2019-02-01 | 2020-08-06 | Pfizer Inc. | Combination of a cdk inhibitor and a pim inhibitor |
| WO2020240360A1 (en) | 2019-05-24 | 2020-12-03 | Pfizer Inc. | Combination therapies using cdk inhibitors |
| JP2022534889A (ja) | 2019-05-24 | 2022-08-04 | ファイザー・インコーポレイテッド | Cdk阻害剤を使用した組合せ療法 |
| CN110256424A (zh) * | 2019-07-03 | 2019-09-20 | 武汉工程大学 | 一种帕博西尼关键中间体v的合成方法 |
| MX2022002415A (es) | 2019-08-26 | 2022-03-22 | Arvinas Operations Inc | Metodos de tratamiento del cancer de mama con derivados de tetrahidronaftaleno como degradadores del receptor de estrogenos. |
| CN110551063A (zh) * | 2019-10-17 | 2019-12-10 | 山东邹平大展新材料有限公司 | 一种合成5-(n-boc-哌嗪-1-基)吡啶-2-胺的方法 |
| TW202146017A (zh) | 2020-03-05 | 2021-12-16 | 美商輝瑞股份有限公司 | 間變性淋巴瘤激酶抑制劑及周期蛋白依賴型激酶抑制劑之組合 |
| PT4181920T (pt) | 2020-07-15 | 2025-11-04 | Ctxt Pty Ltd | Inibidor de kat6 e combinações para o tratamento do cancro da mama |
| CA3189632A1 (en) | 2020-07-20 | 2022-01-27 | Pfizer Inc. | Combination therapy |
| CN114306245A (zh) | 2020-09-29 | 2022-04-12 | 深圳市药欣生物科技有限公司 | 无定形固体分散体的药物组合物及其制备方法 |
| WO2022091001A1 (en) | 2020-10-29 | 2022-05-05 | Pfizer Ireland Pharmaceuticals | Process for preparation of palbociclib |
| CN112274493A (zh) * | 2020-11-18 | 2021-01-29 | 石药集团中奇制药技术(石家庄)有限公司 | 一种哌柏西利胶囊的制备方法 |
| CN112457311B (zh) * | 2020-12-04 | 2022-07-12 | 江苏豪森药业集团有限公司 | 一种含有氯溴吡咯嘧啶酮结构化合物的制备方法 |
| WO2022123419A1 (en) | 2020-12-08 | 2022-06-16 | Pfizer Inc. | Treatment of luminal subtypes of hr-positive, her2-negative early breast cancer with palbociclib |
| CN112661753B (zh) * | 2020-12-29 | 2022-06-03 | 山东铂源药业股份有限公司 | 一种帕布昔利布中间体的制备方法 |
| CN112778303A (zh) * | 2020-12-31 | 2021-05-11 | 武汉九州钰民医药科技有限公司 | Cdk4/6激酶抑制剂shr6390的制备方法 |
| CN112898299B (zh) * | 2021-01-26 | 2021-11-26 | 山东铂源药业有限公司 | 一种帕布昔利布中间体的制备方法 |
| WO2022266070A1 (en) | 2021-06-14 | 2022-12-22 | Preh Holding, Llc | Connected body surface care module |
| CN113845520A (zh) * | 2021-09-09 | 2021-12-28 | 安徽皓元药业有限公司 | 一种帕布昔利布乳清酸盐及其制备方法 |
| CN113999227A (zh) * | 2021-11-26 | 2022-02-01 | 常州大学 | 一种帕博西尼中间体的制备方法 |
| WO2023107525A1 (en) | 2021-12-10 | 2023-06-15 | Eli Lilly And Company | Cdk4 and 6 inhibitor in combination with fulvestrant for the treatment of hormone receptor-positive, human epidermal growth factor receptor 2-negative advanced or metastatic breast cancer in patients previously treated with a cdk4 and 6 inhibitor |
| WO2023111810A1 (en) | 2021-12-14 | 2023-06-22 | Pfizer Inc. | Combination therapies and uses for treating cancer |
| WO2023114264A1 (en) | 2021-12-15 | 2023-06-22 | Eli Lilly And Company | Combination for treatment of high-risk metastatic hormone-sensitive prostate cancer |
| CN114195784A (zh) * | 2021-12-29 | 2022-03-18 | 斯坦德标准技术研究(湖北)有限公司 | 帕博西尼有关物质及其制备方法和应用 |
| EP4302755B1 (en) | 2022-07-07 | 2025-08-20 | Lotus Pharmaceutical Co., Ltd. | Palbociclib formulation containing an amino acid |
| EP4302832A1 (en) | 2022-07-07 | 2024-01-10 | Lotus Pharmaceutical Co., Ltd. | Palbociclib formulation containing glucono delta lactone |
| JP2025533719A (ja) | 2022-07-29 | 2025-10-09 | ファイザー・インク | がんの治療のためのkat6阻害剤を含む投与レジメン |
| TWI866427B (zh) | 2022-08-31 | 2024-12-11 | 美商亞文納營運公司 | 雌激素受體降解劑之給藥方案 |
| CN120456897A (zh) | 2022-11-02 | 2025-08-08 | 佩特拉制药公司 | 用于治疗疾病的磷酸肌醇3-激酶(pi3k)变构色原酮抑制剂 |
| WO2024132652A1 (en) | 2022-12-22 | 2024-06-27 | Synthon B.V. | Pharmaceutical composition comprising palbociclib |
| WO2024133726A1 (en) | 2022-12-22 | 2024-06-27 | Synthon B.V. | Pharmaceutical composition comprising palbociclib |
| KR20250164842A (ko) | 2023-03-30 | 2025-11-25 | 화이자 인코포레이티드 | Kat6a 억제제에 의한 치료를 위한 예측 바이오마커로서의 kat6a 및 이의 치료 방법 |
| WO2024201340A1 (en) | 2023-03-30 | 2024-10-03 | Pfizer Inc. | Kat6a as a predictive biomarker for treatment of breast cancer with a cdk4 inhibitor and an antiestrogen and methods of treatment thereof |
| WO2025051337A1 (en) | 2023-09-06 | 2025-03-13 | Afyx Development A/S | Compositions and methods for treating and preventing oral cancer |
| TW202532065A (zh) | 2023-12-04 | 2025-08-16 | 美商建南德克公司 | 治療乳癌之組合療法 |
| WO2025202854A1 (en) | 2024-03-27 | 2025-10-02 | Pfizer Inc. | Cdk4 inhibitors and combinations with cdk2 inhibitors or further agents for use in the treatment of cancer |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
| US5376645A (en) | 1990-01-23 | 1994-12-27 | University Of Kansas | Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof |
| GB9518953D0 (en) | 1995-09-15 | 1995-11-15 | Pfizer Ltd | Pharmaceutical formulations |
| WO2000035298A1 (en) | 1996-11-27 | 2000-06-22 | Wm. Wrigley Jr. Company | Chewing gum containing medicament active agents |
| GB9711643D0 (en) | 1997-06-05 | 1997-07-30 | Janssen Pharmaceutica Nv | Glass thermoplastic systems |
| JPH11138004A (ja) * | 1997-11-06 | 1999-05-25 | Mitsui Chem Inc | ニトリル水和用の銅触媒及びその調製方法 |
| CA2401368A1 (en) * | 2000-03-06 | 2001-09-27 | Warner-Lambert Company | 5-alkylpyrido[2,3-d]pyrimidines tyrosine kinase inhibitors |
| PL218692B1 (pl) | 2002-01-22 | 2015-01-30 | Warner Lambert Co | Podstawiony 2-(pirydyn-2-yloamino)pirydo[2,3-d]pirymidyn-7-on oraz jego zastosowanie do leczenia zaburzenia lub stanu spowodowanego nieprawidłową proliferacją komórek |
| JP2004074041A (ja) * | 2002-08-20 | 2004-03-11 | Cabot Supermetal Kk | フッ素の回収方法 |
| JP2004149472A (ja) * | 2002-10-31 | 2004-05-27 | Sumitomo Chem Co Ltd | 亜リン酸エステル類の結晶、及びその製造方法 |
| AU2004255934B2 (en) * | 2003-07-11 | 2010-02-25 | Warner-Lambert Company Llc | Isethionate salt of a selective CDK4 inhibitor |
| CA2572325C (en) * | 2004-06-29 | 2013-08-27 | Sapphire Therapeutics, Inc. | Crystal forms of (3r)-1-(2-methylalanyl-d-tryptophyl)-3-(phenylmethyl)-3-piperidinecarboxylic acid 1,2,2-trimethylhydrazide |
| GT200600315A (es) * | 2005-07-20 | 2007-03-19 | Formas cristalinas de 4-metilo-n-[3-(4-metilo-imidazol-1-ilo)-5-trifluorometilo-fenilo]-3-(4-pyridina-3-ilo-pirimidina-2-iloamino)-benzamida | |
| EP2069344A2 (en) * | 2006-09-08 | 2009-06-17 | Pfizer Products Inc. | Synthesis of 2-(pyridin-2-ylamino)-pyrido[2,3-d]pyrimidin-7-ones |
| EP2185559A1 (en) * | 2007-08-03 | 2010-05-19 | Boehringer Ingelheim International GmbH | Crystalline form of a dihydropteridione derivative |
| TW201014830A (en) * | 2008-09-30 | 2010-04-16 | Theravance Inc | Crystalline form of an alkoxyimidazol-1-ylmethyl biphenyl carboxylic acid |
| PL2453894T3 (pl) * | 2009-07-15 | 2016-04-29 | Theravance Biopharma R&D Ip Llc | Postać krystaliczna wolnej zasady związku bifenylowego |
| EP2477972A1 (en) * | 2009-09-20 | 2012-07-25 | Abbott Laboratories | Abt-263 crystalline forms and solvates for use in treating bcl-2 protein related diseases |
| CZ201039A3 (cs) | 2010-01-19 | 2011-07-27 | Zentiva, K. S | Zpusob prumyslové výroby amorfní formy hemivápenaté soli (3R,5R) 7-[3-fenyl-4-fenylkarbamoyl-2-(4-fluorfenyl)-5-isopropylpyrrol-1-yl]-3,5-dihydroxyheptanové kyseliny (atorvastatinu) s vysokým specifickým povrchem a jeho použití v lékové forme |
| PH12013500934A1 (en) * | 2010-11-09 | 2022-10-24 | Zafgen Inc | Crystalline solids of a metap-2 inhibitor and methods of making and using same |
| EP3431475B1 (en) * | 2013-02-21 | 2021-04-07 | Pfizer Inc | Solid forms of a selective cdk4/6 inhibitor |
| EP3180007A1 (en) | 2014-08-14 | 2017-06-21 | Sun Pharmaceutical Industries Ltd | Crystalline forms of palbociclib |
-
2014
- 2014-02-08 EP EP18186675.7A patent/EP3431475B1/en not_active Revoked
- 2014-02-08 EP EP14705884.6A patent/EP2958916B1/en not_active Revoked
- 2014-02-08 SI SI201430929T patent/SI2958916T1/sl unknown
- 2014-02-08 DK DK18186675.7T patent/DK3431475T3/da active
- 2014-02-08 TR TR2018/16077T patent/TR201816077T4/tr unknown
- 2014-02-08 RU RU2015132371A patent/RU2619944C2/ru active
- 2014-02-08 KR KR1020157022487A patent/KR20150107872A/ko not_active Abandoned
- 2014-02-08 MX MX2015010858A patent/MX363715B/es unknown
- 2014-02-08 KR KR1020177022021A patent/KR101858913B1/ko active Active
- 2014-02-08 ES ES18186675T patent/ES2869277T3/es active Active
- 2014-02-08 CA CA2900322A patent/CA2900322C/en active Active
- 2014-02-08 WO PCT/IB2014/058865 patent/WO2014128588A1/en not_active Ceased
- 2014-02-08 CN CN201711141072.8A patent/CN107759594A/zh active Pending
- 2014-02-08 PL PL14705884T patent/PL2958916T3/pl unknown
- 2014-02-08 CN CN202010094827.9A patent/CN111253394A/zh active Pending
- 2014-02-08 BR BR112015019508A patent/BR112015019508A8/pt not_active Application Discontinuation
- 2014-02-08 PT PT181866757T patent/PT3431475T/pt unknown
- 2014-02-08 PT PT14705884T patent/PT2958916T/pt unknown
- 2014-02-08 SG SG11201505680RA patent/SG11201505680RA/en unknown
- 2014-02-08 SI SI201431819T patent/SI3431475T1/sl unknown
- 2014-02-08 PL PL18186675T patent/PL3431475T3/pl unknown
- 2014-02-08 MX MX2019003605A patent/MX386473B/es unknown
- 2014-02-08 CN CN201480009556.5A patent/CN105008357A/zh active Pending
- 2014-02-08 AU AU2014220354A patent/AU2014220354B2/en active Active
- 2014-02-08 HK HK15111953.5A patent/HK1211032A1/xx unknown
- 2014-02-08 ES ES14705884.6T patent/ES2694787T3/es active Active
- 2014-02-08 US US14/769,038 patent/US20160002223A1/en not_active Abandoned
- 2014-02-08 HU HUE14705884A patent/HUE040434T2/hu unknown
- 2014-02-08 HU HUE18186675A patent/HUE054212T2/hu unknown
- 2014-02-08 DK DK14705884.6T patent/DK2958916T3/en active
- 2014-02-18 TW TW106131041A patent/TWI670269B/zh active
- 2014-02-18 TW TW103105287A patent/TWI633103B/zh active
- 2014-02-18 JP JP2014028092A patent/JP6381016B2/ja active Active
- 2014-02-20 AR ARP140100540A patent/AR094842A1/es unknown
-
2015
- 2015-07-30 IL IL24027715A patent/IL240277B/en active IP Right Review Request
- 2015-12-03 HK HK18107562.3A patent/HK1248217A1/zh unknown
-
2017
- 2017-07-18 JP JP2017139197A patent/JP6524152B2/ja active Active
- 2017-11-09 US US15/808,577 patent/US10723730B2/en active Active
-
2018
- 2018-10-05 CY CY181101034T patent/CY1120734T1/el unknown
-
2019
- 2019-04-26 JP JP2019085273A patent/JP2019116512A/ja active Pending
-
2021
- 2021-04-16 CY CY20211100336T patent/CY1124068T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CY1124068T1 (el) | Στερεες μορφες ενος εκλεκτικου αναστολεα cdk4/6 | |
| CY1124928T1 (el) | Αναστολεις πυραζολυλο κινοξαλινο κινασης | |
| CY1125436T1 (el) | Αναστολεις dna-pk | |
| CY1124311T1 (el) | Παρεμποδιστες dna-pk | |
| CY1124000T1 (el) | Υποκατεστημενες 5-φθορο-1η-πυραζολοπυριδινες σε κρυσταλλικη μορφη | |
| CY1123756T1 (el) | Παραγωγα διπυραζολιου ως αναστολεις jak | |
| CY1122712T1 (el) | ΧΡΗΣΗ ΠΑΡΑΓΩΓΩΝ ΠΥΡΑΖΟΛΟΠΥΡΙΜΙΔΙΝΗΣ ΓΙΑ ΤΗ ΘΕΡΑΠΕΙΑ ΣΧΕΤΙΚΩΝ ΜΕ PI3Kδ ΔΙΑΤΑΡΑΧΩΝ | |
| CY1123595T1 (el) | Παραγωγα χολικου οξεος ως αγωνιστες fxr/tgr5 | |
| CY1120031T1 (el) | Αποπτωτικοι υποκινητες ν-ακυλοσουλφοναμιδης | |
| CY1122266T1 (el) | Ενωσεις 3-αμινοκυκλοαλκυλιου ως ror-gamma-t αναστολεις και χρησεις αυτων | |
| CY1122730T1 (el) | 1,2,4-τριαζολες ως διαμορφωτες πυρηνικης μεταφορας και χρησεις αυτων | |
| CY1121150T1 (el) | Νευροδραστικα 19-αλκοξυ-17-υποκατεστημενα στεροειδη, χρησιμα σε μεθοδους θεραπειας | |
| CY1122601T1 (el) | Αναστολεις gsk3 και μεθοδοι χρησης αυτων | |
| EA201290980A1 (ru) | Производные 1-амино-2-циклопропилэтилбороновой кислоты | |
| CY1123689T1 (el) | Κρυσταλλικη μορφη ελευθερης βασης λορλατινιβης | |
| EA201491399A1 (ru) | Селективные ингибиторы cdk8/cdk19 и их применение в качестве противометастатических и химиопрофилактических агентов для лечения рака | |
| EA201500926A1 (ru) | Фумараты как пролекарства и их применение при лечении различных заболеваний | |
| EA201391285A1 (ru) | Производные тетрагидрохинолина, полезные в качестве ингибиторов бромодомена | |
| EA201591591A1 (ru) | Соединения карбазола, применяемые в качестве ингибиторов бромодомена | |
| EA201592200A1 (ru) | Производные сульфамоилпирроламида и их применение в качестве медикаментов для лечения гепатита b | |
| CY1120204T1 (el) | Αμορφη στερεα διασπορα για χρηση σε θεραπεια καρκινου του εγκεφαλο | |
| EA201591406A1 (ru) | C-19 модифицированные тритерпеноиды с ингибиторной активностью созревания вич | |
| DOP2015000170A (es) | Compuestos químicos | |
| EA201591456A1 (ru) | Макроциклические и бициклические ингибиторы вируса гепатита с | |
| EA201591904A1 (ru) | НОВЫЕ ПРОИЗВОДНЫЕ N-(2,3-ДИГИДРО-1H-ПИРРОЛО[2,3-b]ПИРИДИН-5-ИЛ)-4-ХИНАЗОЛИНАМИНА И N-(2,3-ДИГИДРО-1H-ИНДОЛ-5-ИЛ)-4-ХИНАЗОЛИНАМИНА В КАЧЕСТВЕ ИНГИБИТОРОВ PERK |