MX363715B - Formas solidas de un inhbidor de cdk4/6 selectivo. - Google Patents

Formas solidas de un inhbidor de cdk4/6 selectivo.

Info

Publication number
MX363715B
MX363715B MX2015010858A MX2015010858A MX363715B MX 363715 B MX363715 B MX 363715B MX 2015010858 A MX2015010858 A MX 2015010858A MX 2015010858 A MX2015010858 A MX 2015010858A MX 363715 B MX363715 B MX 363715B
Authority
MX
Mexico
Prior art keywords
inhibitor
solid forms
selective cdk4
dosage forms
free base
Prior art date
Application number
MX2015010858A
Other languages
English (en)
Spanish (es)
Other versions
MX2015010858A (es
Inventor
Brian Patrick Chekal
Nathan D Ide
Original Assignee
Pfizer
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=50151343&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MX363715(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer filed Critical Pfizer
Publication of MX2015010858A publication Critical patent/MX2015010858A/es
Publication of MX363715B publication Critical patent/MX363715B/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline 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)
MX2015010858A 2013-02-21 2014-02-08 Formas solidas de un inhbidor de cdk4/6 selectivo. MX363715B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361767761P 2013-02-21 2013-02-21
PCT/IB2014/058865 WO2014128588A1 (en) 2013-02-21 2014-02-08 Solid forms of a selective cdk4/6 inhibitor

Publications (2)

Publication Number Publication Date
MX2015010858A MX2015010858A (es) 2015-12-03
MX363715B true MX363715B (es) 2019-03-29

Family

ID=50151343

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2019003605A MX386473B (es) 2013-02-21 2014-02-08 Formas solidas de un inhibidor de cdk4/6 selectivo
MX2015010858A MX363715B (es) 2013-02-21 2014-02-08 Formas solidas de un inhbidor de cdk4/6 selectivo.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MX2019003605A MX386473B (es) 2013-02-21 2014-02-08 Formas solidas de un inhibidor de cdk4/6 selectivo

Country Status (24)

Country Link
US (2) US20160002223A1 (enExample)
EP (2) EP2958916B1 (enExample)
JP (3) JP6381016B2 (enExample)
KR (2) KR101858913B1 (enExample)
CN (3) CN107759594A (enExample)
AR (1) AR094842A1 (enExample)
AU (1) AU2014220354B2 (enExample)
BR (1) BR112015019508A8 (enExample)
CA (1) CA2900322C (enExample)
CY (2) CY1120734T1 (enExample)
DK (2) DK3431475T3 (enExample)
ES (2) ES2694787T3 (enExample)
HK (2) HK1211032A1 (enExample)
HU (2) HUE040434T2 (enExample)
IL (1) IL240277B (enExample)
MX (2) MX386473B (enExample)
PL (2) PL2958916T3 (enExample)
PT (2) PT3431475T (enExample)
RU (1) RU2619944C2 (enExample)
SG (1) SG11201505680RA (enExample)
SI (2) SI2958916T1 (enExample)
TR (1) TR201816077T4 (enExample)
TW (2) TWI633103B (enExample)
WO (1) WO2014128588A1 (enExample)

Families Citing this family (109)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2019102203A (ru) 2012-07-11 2019-03-05 Блюпринт Медсинс Корпорейшн Ингибиторы рецептора фактора роста фибробластов
HUE040434T2 (hu) * 2013-02-21 2019-03-28 Pfizer Szelektív CDK4/6 inhibitor szilárd alakjai
PT3395814T (pt) 2013-10-25 2022-07-27 Blueprint Medicines Corp Inibidores do recetor do fator de crescimento de fibroblastos
WO2015108992A1 (en) 2014-01-15 2015-07-23 Blueprint Medicines Corporation Heterobicyclic compounds and their use as fgfr4 receptor inhibitors
EP3180007A1 (en) * 2014-08-14 2017-06-21 Sun Pharmaceutical Industries Ltd Crystalline forms of palbociclib
EP3186252A1 (en) * 2014-08-28 2017-07-05 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
EP3078663A1 (en) 2015-04-09 2016-10-12 Sandoz Ag Modified particles of palbociclib
WO2016156070A1 (en) 2015-04-02 2016-10-06 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
KR102068423B1 (ko) * 2015-06-04 2020-01-20 화이자 인코포레이티드 팔보시클립의 고체 투여 형태
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
EP3543235A1 (en) 2015-08-05 2019-09-25 ratiopharm GmbH Crystalline form and acetic acid adduct 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
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
US20170129902A1 (en) 2015-10-16 2017-05-11 Abbvie Inc. PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-alpha]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
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
GB201601329D0 (en) 2016-01-25 2016-03-09 Mohammad Mohammad A Inverse gas chromatography standard solutions, device and method
WO2017130219A1 (en) 2016-01-25 2017-08-03 Mylan Laboratories Limited Amorphous solid dispersion of palbociclib
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
UA124804C2 (uk) 2016-08-15 2021-11-24 Пфайзер Інк. Піридопіримідинонові інгібітори cdk2/4/6
US20190192522A1 (en) 2016-09-08 2019-06-27 Blueprint Medicines Corporation Inhibitors of the fibroblast growth factor receptor 4 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
CA3043681A1 (en) 2016-11-16 2018-05-24 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
CN110382495B (zh) 2016-12-16 2022-04-05 基石药业(苏州)有限公司 Cdk4/6抑制剂
WO2018191950A1 (en) * 2017-04-21 2018-10-25 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
US11168326B2 (en) 2017-07-11 2021-11-09 Actym Therapeutics, Inc. Engineered immunostimulatory bacterial strains and uses thereof
WO2019020715A1 (en) 2017-07-28 2019-01-31 Synthon B.V. PHARMACEUTICAL COMPOSITION COMPRISING PALBOCICLIB
TWI785098B (zh) 2017-08-18 2022-12-01 開曼群島商科賽睿生命科學公司 Tg02之多晶型
JP7100125B2 (ja) 2017-10-27 2022-07-12 フレゼニウス・カビ・オンコロジー・リミテッド リボシクリブおよびその塩の改善された調製のためのプロセス
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
WO2019136451A1 (en) 2018-01-08 2019-07-11 G1 Therapeutics, Inc. G1t38 superior dosage regimes
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
WO2019166928A1 (en) 2018-02-27 2019-09-06 Pfizer Inc. Combination of a cyclin dependent kinase inhibitor and a bet-bromodomain inhibitor
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
EP3793609B1 (en) 2018-05-14 2023-12-13 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
EP3844276A2 (en) 2018-08-28 2021-07-07 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
WO2020239558A1 (en) 2019-05-24 2020-12-03 Pfizer Inc. Combination therapies using cdk inhibitors
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
KR20220054347A (ko) 2019-08-26 2022-05-02 아비나스 오퍼레이션스, 인코포레이티드 에스트로겐 수용체 분해제로서의 테트라히드로나프탈렌 유도체로 유방암을 치료하는 방법
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
US20230117684A1 (en) 2020-03-05 2023-04-20 Pfizer Inc. Combination of an anaplastic lymphoma kinase inhibitor and a cyclin dependent kinase inhibitor
EP4181920B1 (en) 2020-07-15 2025-09-10 Pfizer Inc. Kat6 inhibitor and combinations for breast cancer treatment
JP2022020583A (ja) 2020-07-20 2022-02-01 ファイザー・インク 併用療法
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
EP4356398A4 (en) 2021-06-14 2025-04-16 Preh Holding, LLC CONNECTED BODY SURFACE CARE MODULE
EP4370126A4 (en) 2021-07-16 2025-05-28 Dana-Farber Cancer Institute, Inc. Small molecule cyclin dependent kinase 4/6 (cdk4/6) and ikzf2 (helios) degraders and methods of use thereof
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
KR20240118134A (ko) 2021-12-10 2024-08-02 일라이 릴리 앤드 캄파니 Cdk4 및 6 억제제로 이전에 치료된 환자에서의 호르몬 수용체-양성, 인간 표피 성장 인자 수용체 2-음성 진행성 또는 전이성 유방암의 치료를 위한 풀베스트란트와 조합된 cdk4 및 6 억제제
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
CN119604288A (zh) 2022-07-29 2025-03-11 辉瑞大药厂 用于治疗癌症的包含kat6抑制剂的给药方案
EP4580631A1 (en) 2022-08-31 2025-07-09 Arvinas Operations, Inc. Dosage regimens of estrogen receptor degraders
JP2024067010A (ja) 2022-11-02 2024-05-16 ペトラ・ファーマ・コーポレイション 疾患の治療用のホスホイノシチド3-キナーゼ(pi3k)のアロステリッククロメノン阻害剤
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
WO2025122470A1 (en) 2023-12-04 2025-06-12 Genentech, Inc. Combination therapies for treatment of breast cancer
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)

* Cited by examiner, † Cited by third party
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
DZ3308A1 (fr) * 2000-03-06 2001-09-27 Warner Lambert Co Inhibiteurs de tyrosine kinase a base de 5-alkylpyrido [2,3-d] pyrimidines
GEP20063909B (en) * 2002-01-22 2006-08-25 Warner Lambert Co 2-(PYRIDIN-2-YLAMINO)-PYRIDO[2,3d] PYRIMIDIN-7-ONES
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
ATE412650T1 (de) 2003-07-11 2008-11-15 Warner Lambert Co Isethionat salz eines selektiven cdk4 inhibitors
KR101324340B1 (ko) * 2004-06-29 2013-10-31 헬신 세라퓨틱스 (유.에스.) 인크. (3r)-1-(2-메틸알라닐-d-트립토필)-3-(페닐메틸)-3-피페리딘카르복실산 1,2,2-트리메틸하이드라지드의 결정 형태
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
HUE026414T2 (hu) * 2009-07-15 2016-05-30 Theravance Biopharma R&D Ip Llc Bifenil-vegyület kristályos szabad-bázis formája
JP2013505249A (ja) * 2009-09-20 2013-02-14 アボット・ラボラトリーズ Bcl−2タンパク質関連疾患の治療における使用のためのABT−263結晶形態および溶媒和物
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
HUE040434T2 (hu) 2013-02-21 2019-03-28 Pfizer Szelektív CDK4/6 inhibitor szilárd alakjai
EP3180007A1 (en) 2014-08-14 2017-06-21 Sun Pharmaceutical Industries Ltd Crystalline forms of palbociclib

Also Published As

Publication number Publication date
US20160002223A1 (en) 2016-01-07
SG11201505680RA (en) 2015-09-29
PL2958916T3 (pl) 2019-01-31
IL240277B (en) 2019-10-31
NZ710138A (en) 2020-09-25
WO2014128588A1 (en) 2014-08-28
US20180065964A1 (en) 2018-03-08
TW201803872A (zh) 2018-02-01
CN105008357A (zh) 2015-10-28
EP2958916B1 (en) 2018-09-12
PL3431475T3 (pl) 2021-09-13
HUE040434T2 (hu) 2019-03-28
RU2619944C2 (ru) 2017-05-22
BR112015019508A2 (pt) 2017-07-18
SI2958916T1 (sl) 2018-11-30
HK1211032A1 (en) 2016-05-13
TWI670269B (zh) 2019-09-01
MX2019003605A (es) 2019-06-17
TR201816077T4 (tr) 2018-11-21
TW201444834A (zh) 2014-12-01
RU2015132371A (ru) 2017-03-29
DK3431475T3 (da) 2021-05-25
JP6524152B2 (ja) 2019-06-05
ES2694787T3 (es) 2018-12-27
JP6381016B2 (ja) 2018-08-29
KR20170094012A (ko) 2017-08-16
CA2900322C (en) 2019-03-26
PT2958916T (pt) 2018-11-21
HK1248217A1 (zh) 2018-10-12
EP3431475A1 (en) 2019-01-23
MX386473B (es) 2025-03-18
AU2014220354A1 (en) 2015-08-06
CY1120734T1 (el) 2019-12-11
ES2869277T3 (es) 2021-10-25
JP2019116512A (ja) 2019-07-18
MX2015010858A (es) 2015-12-03
CY1124068T1 (el) 2022-05-27
KR20150107872A (ko) 2015-09-23
PT3431475T (pt) 2021-05-13
IL240277A0 (en) 2015-09-24
JP2017186376A (ja) 2017-10-12
AR094842A1 (es) 2015-09-02
HUE054212T2 (hu) 2021-08-30
JP2014162794A (ja) 2014-09-08
EP3431475B1 (en) 2021-04-07
BR112015019508A8 (pt) 2019-11-19
US10723730B2 (en) 2020-07-28
SI3431475T1 (sl) 2021-08-31
DK2958916T3 (en) 2018-11-12
CA2900322A1 (en) 2014-08-28
TWI633103B (zh) 2018-08-21
KR101858913B1 (ko) 2018-05-16
EP2958916A1 (en) 2015-12-30
CN111253394A (zh) 2020-06-09
CN107759594A (zh) 2018-03-06
AU2014220354B2 (en) 2018-02-01

Similar Documents

Publication Publication Date Title
MX363715B (es) Formas solidas de un inhbidor de cdk4/6 selectivo.
PH12015502615B1 (en) Chemical compounds
NZ630925A (en) Pyrazolopyrimidine compounds as kinase inhibitors
MX359418B (es) Pteridinas como inhibidores del receptor del factor de crecimiento de fribroblasto (fgfr).
MX336214B (es) Derivados de pirrolotriazinona como inhibidores de pi3k.
MY185666A (en) Anticancer pyridopyrazines via the inhibition of fgfr kinases
PH12012502334A1 (en) Heteroaryl imidazolone derivatives as jak inhibitors
MX349004B (es) Nuevos compuestos.
EA201290147A1 (ru) Пирроло[2,3-d]пиримидиновые соединения
MX368112B (es) Pirrolo- o pirazolopirimidinas covalentes reversibles utiles para el tratamiento del cancer y de enfermedades autoinmunitarias.
PH12014500103A1 (en) Pyridin-2(1h)-one derivatives as jak inhibitors
GB201205669D0 (en) Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof
MX2015014234A (es) Derivados 2-aminopirido-[4,3-d]pirimidin-5-ona y su uso como inhibidores de wee-1.
MX2015012414A (es) Sal de omecamtiv mecarbilo y proceso para preparar la sal.
PH12015500813B1 (en) Pyrrolotriazinone derivatives as pi3k inhibitors
MX366899B (es) Nuevos compuestos.
JO3115B1 (ar) مركبات بيريدازينون واستخدامها كمثبطات daao
MX2012009074A (es) Compuestos de urea pirrolo [2, 3-d] pirimidina como inhibidores de janus quinasa.
TW201613864A (en) Novel compounds
MX2016003522A (es) Derivados de quinazolinas y su uso como inhibidores de la adn metiltransferasa.
WO2016010869A3 (en) FUSED QUINOLINE COMPUNDS AS PI3K, mTOR INHIBITORS
TN2013000377A1 (en) Thieno [2, 3-d] pyrimidine derivatives and their use to treat arrhythmia