JP2015010091A5 - - Google Patents

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Publication number
JP2015010091A5
JP2015010091A5 JP2014124999A JP2014124999A JP2015010091A5 JP 2015010091 A5 JP2015010091 A5 JP 2015010091A5 JP 2014124999 A JP2014124999 A JP 2014124999A JP 2014124999 A JP2014124999 A JP 2014124999A JP 2015010091 A5 JP2015010091 A5 JP 2015010091A5
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JP
Japan
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ppm
crystalline
value
powder
values
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JP2014124999A
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English (en)
Japanese (ja)
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JP6110817B2 (ja
JP2015010091A (ja
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Publication of JP2015010091A5 publication Critical patent/JP2015010091A5/ja
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Publication of JP6110817B2 publication Critical patent/JP6110817B2/ja
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JP2014124999A 2013-06-28 2014-06-18 大環状キナーゼ阻害剤の固体形態 Active JP6110817B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361840703P 2013-06-28 2013-06-28
US61/840,703 2013-06-28

Publications (3)

Publication Number Publication Date
JP2015010091A JP2015010091A (ja) 2015-01-19
JP2015010091A5 true JP2015010091A5 (OSRAM) 2016-08-04
JP6110817B2 JP6110817B2 (ja) 2017-04-05

Family

ID=51136530

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014124999A Active JP6110817B2 (ja) 2013-06-28 2014-06-18 大環状キナーゼ阻害剤の固体形態

Country Status (8)

Country Link
US (1) US9637500B2 (OSRAM)
EP (1) EP3013835B1 (OSRAM)
JP (1) JP6110817B2 (OSRAM)
AR (1) AR096759A1 (OSRAM)
CA (1) CA2916605C (OSRAM)
ES (1) ES2656189T3 (OSRAM)
TW (1) TW201504246A (OSRAM)
WO (1) WO2014207606A1 (OSRAM)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016026423A1 (en) * 2014-08-20 2016-02-25 Teligene Ltd Substituted macrocycles useful as kinases inhibitors and methods of use thereof
US10159663B2 (en) * 2014-08-20 2018-12-25 Teligene Ltd. Substituted macrocycles useful as kinases inhibitors and methods of use thereof
MX382600B (es) 2015-07-31 2025-03-13 Pfizer Forma cristalina de base libre de lorlatinib.
CA3000386A1 (en) 2015-09-30 2017-04-06 Merck Patent Gmbh Combination of a pd-1 axis binding antagonist and an alk inhibitor for treating alk-negative cancer
EP3763693A1 (en) 2016-03-03 2021-01-13 Shenzhen TargetRx, Inc. Macrocycle and composition comprising thereof
EP3440086B1 (en) 2016-04-08 2020-08-12 Pfizer Inc. Crystalline forms of lorlatinib maleate
WO2019073347A1 (en) * 2017-10-10 2019-04-18 Pfizer Inc. CRYSTALLINE BASE FREE HYDRATE SHAPE OF LORLATINIB
US11179412B2 (en) 2017-12-04 2021-11-23 University of Pittsburgh—of the Commonwealth System of Higher Education Methods of treating conditions involving elevated inflammatory response
EP3784675A1 (en) 2018-04-23 2021-03-03 Pliva Hrvatska D.O.O. Solid state forms of lorlatinib and their preparation
WO2020108522A1 (zh) * 2018-11-28 2020-06-04 深圳市塔吉瑞生物医药有限公司 一种氘代大环化合物的制备方法
CN109651398B (zh) * 2019-01-25 2021-07-30 安庆多辉生物科技有限公司 一种合成劳拉替尼的溴代物中间体及催化合成劳拉替尼的方法
EP3999514A1 (en) * 2019-07-18 2022-05-25 Pliva Hrvatska D.O.O. Crystalline lorlatinib : fumaric acid and solid state form thereof
CN112321604A (zh) * 2019-08-05 2021-02-05 华东理工大学 大环类jak2抑制剂及其应用
CN110483551B (zh) * 2019-08-30 2021-10-22 北京赛思源生物医药技术有限公司 一种劳拉替尼游离碱的晶体
EP4041396A1 (en) 2019-10-10 2022-08-17 Sandoz AG Polymorph of lorlatinib
CN112824417A (zh) * 2019-11-21 2021-05-21 上海天慈国际药业有限公司 一种劳拉替尼的制备方法
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
AU2021268345A1 (en) 2020-05-05 2022-11-10 Nuvalent, Inc. Heteroaromatic macrocyclic ether chemotherapeutic agents
WO2021226208A2 (en) 2020-05-05 2021-11-11 Nuvalent, Inc. Heteroaromatic macrocyclic ether chemotherapeutic agents
CN112724077B (zh) * 2020-12-29 2023-07-11 武汉利昌医药科技有限公司 一种劳拉替尼中间体的合成方法
CN113292496B (zh) * 2021-05-17 2023-03-10 安徽联创生物医药股份有限公司 一种劳拉替尼中间体的合成方法
KR20240087788A (ko) 2021-10-01 2024-06-19 뉴베일런트, 아이엔씨. 헤테로방향족 매크로사이클릭 에테르 화합물의 고체 형태, 약학 조성물 및 제조

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011138751A2 (en) * 2010-05-04 2011-11-10 Pfizer Inc. Heterocyclic derivatives as alk inhibitors
EP2822953B9 (en) 2012-03-06 2017-06-21 Pfizer Inc Macrocyclic derivatives for the treatment of proliferative diseases

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