PL3178817T3 - Postać amorficzna związku tetracyklicznego - Google Patents

Postać amorficzna związku tetracyklicznego

Info

Publication number
PL3178817T3
PL3178817T3 PL15830197T PL15830197T PL3178817T3 PL 3178817 T3 PL3178817 T3 PL 3178817T3 PL 15830197 T PL15830197 T PL 15830197T PL 15830197 T PL15830197 T PL 15830197T PL 3178817 T3 PL3178817 T3 PL 3178817T3
Authority
PL
Poland
Prior art keywords
amorphous form
tetracyclic compound
tetracyclic
compound
amorphous
Prior art date
Application number
PL15830197T
Other languages
English (en)
Inventor
Koji Shiraki
Tadanobu Nakayama
Tomoaki Ota
Original Assignee
Chugai Seiyaku Kabushiki Kaisha
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
Application filed by Chugai Seiyaku Kabushiki Kaisha filed Critical Chugai Seiyaku Kabushiki Kaisha
Publication of PL3178817T3 publication Critical patent/PL3178817T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/32Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/38Cellulose; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Plural Heterocyclic Compounds (AREA)
PL15830197T 2014-08-08 2015-08-07 Postać amorficzna związku tetracyklicznego PL3178817T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2014162899 2014-08-08
PCT/JP2015/072450 WO2016021707A1 (ja) 2014-08-08 2015-08-07 4環性化合物の非晶質体
EP15830197.8A EP3178817B1 (en) 2014-08-08 2015-08-07 Amorphous form of tetracyclic compound

Publications (1)

Publication Number Publication Date
PL3178817T3 true PL3178817T3 (pl) 2020-11-16

Family

ID=55263964

Family Applications (1)

Application Number Title Priority Date Filing Date
PL15830197T PL3178817T3 (pl) 2014-08-08 2015-08-07 Postać amorficzna związku tetracyklicznego

Country Status (8)

Country Link
US (4) US10344014B2 (pl)
EP (2) EP3660009A1 (pl)
JP (3) JP6906308B2 (pl)
DK (1) DK3178817T3 (pl)
ES (1) ES2803577T3 (pl)
PL (1) PL3178817T3 (pl)
TW (4) TWI765410B (pl)
WO (1) WO2016021707A1 (pl)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4588121B1 (ja) * 2009-06-10 2010-11-24 中外製薬株式会社 4環性化合物
AU2011291708B2 (en) 2010-08-20 2015-03-19 Chugai Seiyaku Kabushiki Kaisha Composition containing tetracyclic compound
DK2902029T3 (en) 2012-09-25 2018-10-29 Chugai Pharmaceutical Co Ltd RET INHIBITOR
EP3135287A4 (en) 2014-04-25 2018-01-03 Chugai Seiyaku Kabushiki Kaisha Preparation containing tetracyclic compound at high dose
RU2720680C2 (ru) 2014-06-18 2020-05-12 Ф. Хоффманн-Ля Рош Аг Новая фармацевтическая композиция, содержащая неионные сурфактанты
TWI765410B (zh) 2014-08-08 2022-05-21 日商中外製藥股份有限公司 4環性化合物的非晶質體的用途
CN106999432A (zh) 2014-12-05 2017-08-01 阿拉贡药品公司 抗癌组合物
RU2740261C2 (ru) 2015-01-16 2021-01-12 Чугаи Сейяку Кабусики Кайся Комбинированное лекарственное средство
CN109219437A (zh) * 2016-06-03 2019-01-15 阿拉贡药品公司 抗癌组合物
CN110494422A (zh) 2017-03-15 2019-11-22 太阳制药先进研究有限公司 4-甲基-3-喹啉-3-基乙炔基-苯甲酸n’-(2-氯-6-甲基-苯甲酰基)酰肼的新型无定形分散体
EP3596049A4 (en) * 2017-03-15 2021-01-13 Sun Pharma Advanced Research Company Limited NEW AMORPHIC DISPERSION OF CYCLOPROPANECARBOXYLIC ACID (5- {5- [N '- (2-CHLORO-6-METHYLBENZOYL) HYDRAZINOCARBONYL] -2-METHYL-PHENYLETHYNYL} -PYRIDIN-2-AMIDE
WO2019008520A1 (en) 2017-07-05 2019-01-10 Fresenius Kabi Oncology Limited PROCESS FOR THE PREPARATION OF ALECTINIB OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
EP3815688B1 (en) * 2018-06-29 2023-12-06 Chugai Seiyaku Kabushiki Kaisha Pharmaceutical composition containing poorly-soluble basic medicine
AR116113A1 (es) 2018-09-04 2021-03-31 Chugai Pharmaceutical Co Ltd Método para fabricar un compuesto tetracíclico
EP3556754A1 (en) 2018-12-07 2019-10-23 Fresenius Kabi iPSUM S.r.l. Process for the preparation of alectinib
EA202191370A1 (ru) * 2018-12-14 2021-09-16 Фуджифилм Корпорэйшн Фармацевтическая композиция и способ ее получения
WO2021040027A1 (ja) * 2019-08-30 2021-03-04 三栄源エフ・エフ・アイ株式会社 非晶質の難水溶性素材を含有する固体組成物、及びその製造方法
CN114466641A (zh) * 2019-08-30 2022-05-10 三荣源有限公司 含有非结晶的水溶性差的材料的固体组合物及其生产方法
AR121187A1 (es) 2019-12-27 2022-04-27 Chugai Pharmaceutical Co Ltd Método para clasificar, evaluar o fabricar lauril sulfato de sodio de materia prima o formulación farmacéutica que lo contiene
WO2022009235A1 (en) * 2020-07-10 2022-01-13 Msn Laboratories Private Limited, R&D Center Process for the preparation of gilteritinib fumarate
JP7419572B2 (ja) 2021-01-29 2024-01-22 中外製薬株式会社 小児がん治療用医薬組成物
WO2022176017A1 (ja) * 2021-02-16 2022-08-25 大塚製薬株式会社 非晶質体及び当該非晶質体を含む組成物
EP4119128A1 (en) * 2021-07-13 2023-01-18 Dr. Falk Pharma Gmbh Pharmaceutical composition for the oral administration of poorly soluble drugs comprising an amorphous solid dispersion
JPWO2023074785A1 (pl) 2021-10-28 2023-05-04
WO2023161233A1 (en) * 2022-02-22 2023-08-31 Synthon B.V. Solid forms of alectinib and alectinib salts
WO2023179774A1 (en) * 2022-03-25 2023-09-28 Shenzhen Pharmacin Co., Ltd. Amorphous solid dispersions and pharmaceutical compositions comprising the same

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2699054A (en) * 1953-10-09 1955-01-11 Lloyd H Conover Tetracycline
JPS4918630B1 (pl) 1970-07-29 1974-05-11
JPH0892090A (ja) 1994-07-26 1996-04-09 Tanabe Seiyaku Co Ltd 医薬組成物
DE69505470T2 (de) 1994-08-04 1999-05-12 F. Hoffmann-La Roche Ag, Basel Pyrrolocarbazol
CA2252701C (en) 1996-05-01 2003-10-28 Mississippi State University Halo-substituted protein kinase c inhibitors
EP1178988B1 (en) 1999-05-14 2007-02-28 The Australian National University Compounds and therapeutic methods
WO2002043704A1 (en) 2000-12-01 2002-06-06 Kyowa Hakko Kogyo Co., Ltd. Composition improved in solubility or oral absorbability
JP2004067606A (ja) * 2002-08-08 2004-03-04 Zensei Yakuhin Kogyo Kk イトラコナゾール経口投与製剤
EP1603567A4 (en) 2003-02-28 2006-10-18 Inotek Pharmaceuticals Corp TETRACYCLIC BENZAMIDE DERIVATIVES AND METHOD OF USE THEREOF
DK1454992T3 (da) 2003-03-07 2006-10-02 Ist Naz Stud Cura Dei Tumori Anaplastisk lymfomakinaseassay, reagenser og sammensætninger deraf
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
AU2004259012C1 (en) 2003-07-23 2012-08-02 Exelixis, Inc. Anaplastic lymphoma kinase modulators and methods of use
US7378414B2 (en) 2003-08-25 2008-05-27 Abbott Laboratories Anti-infective agents
AU2004295061B2 (en) 2003-11-21 2008-11-20 Novartis Ag 1H-imidazoquinoline derivatives as protein kinase inhibitors
CA2548600A1 (en) 2003-12-12 2005-06-23 Merck Frosst Canada & Co. Cathepsin cysteine protease inhibitors
JP4927704B2 (ja) 2004-03-19 2012-05-09 シュペーデル・エクスペリメンタ・アーゲー 有機化合物
US7973061B2 (en) 2004-03-31 2011-07-05 Exelixis, Inc. Anaplastic lymphoma kinase modulators and methods of use
PL1786785T3 (pl) 2004-08-26 2010-08-31 Pfizer Enancjomerycznie czyste związki aminoheteroarylowe jako kinazy białkowe
AU2005288864B2 (en) * 2004-09-30 2012-08-23 Janssen Sciences Ireland Uc HIV inhibiting 5-heterocyclyl pyrimidines
GB0517329D0 (en) 2005-08-25 2005-10-05 Merck Sharp & Dohme Stimulation of neurogenesis
CN101304993A (zh) 2005-11-07 2008-11-12 Irm责任有限公司 作为ppar调节剂的化合物和组合物
CA2647448A1 (en) * 2006-04-12 2007-10-18 Pfizer Limited Pyrrolidine derivatives as modulators of chemokine ccr5 receptors
US7601716B2 (en) 2006-05-01 2009-10-13 Cephalon, Inc. Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors
US8063225B2 (en) 2006-08-14 2011-11-22 Chembridge Corporation Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders
EP1914240B1 (en) 2006-10-11 2009-12-02 Astellas Pharma Inc. EML4-ALK fusion gene
CA2598893C (en) 2006-10-11 2012-04-10 Astellas Pharma Inc. Eml4-alk fusion gene
EP2222647B1 (en) 2006-10-23 2015-08-05 Cephalon, Inc. Fused bicyclic derivatives of 2,4-diaminopyrimidine as alk and c-met inhibitors
WO2008130951A1 (en) 2007-04-17 2008-10-30 Bristol-Myers Squibb Company Fused heterocyclic 11-beta-hydroxysteroid dehydrogenase type i inhibitors
TWI389893B (zh) 2007-07-06 2013-03-21 Astellas Pharma Inc 二(芳胺基)芳基化合物
PT2176231T (pt) 2007-07-20 2016-12-09 Nerviano Medical Sciences Srl Derivados de indazol substituídos activos como inibidores de quinases
CA2932121A1 (en) 2007-11-30 2009-06-11 Newlink Genetics Corporation Ido inhibitors
TW201043269A (en) * 2009-04-14 2010-12-16 Bristol Myers Squibb Co Bioavailable compositions of amorphous alpha-(N-sulfonamido)acetamide compound
KR20120034639A (ko) 2009-05-07 2012-04-12 아스트라제네카 아베 치환된 1-시아노에틸헤테로시클릴카르복스아미드 화합물 750
JP4588121B1 (ja) 2009-06-10 2010-11-24 中外製薬株式会社 4環性化合物
GB0910046D0 (en) 2009-06-10 2009-07-22 Glaxosmithkline Biolog Sa Novel compositions
US8609097B2 (en) 2009-06-10 2013-12-17 Hoffmann-La Roche Inc. Use of an anti-Tau pS422 antibody for the treatment of brain diseases
AU2011291708B2 (en) * 2010-08-20 2015-03-19 Chugai Seiyaku Kabushiki Kaisha Composition containing tetracyclic compound
JP5006987B2 (ja) 2010-11-22 2012-08-22 中外製薬株式会社 4環性化合物を含む医薬
CN102793929B (zh) * 2012-09-07 2013-12-11 上海奥科达生物医药科技有限公司 一种制备稳定非晶态药物制剂的方法
DK2902029T3 (en) 2012-09-25 2018-10-29 Chugai Pharmaceutical Co Ltd RET INHIBITOR
JP2015185406A (ja) 2014-03-25 2015-10-22 トヨタ自動車株式会社 燃料電池システム及び燃料電池の水分量制御方法
CN106458967A (zh) 2014-04-25 2017-02-22 中外制药株式会社 四环化合物的新结晶
EP3135287A4 (en) 2014-04-25 2018-01-03 Chugai Seiyaku Kabushiki Kaisha Preparation containing tetracyclic compound at high dose
RU2720680C2 (ru) 2014-06-18 2020-05-12 Ф. Хоффманн-Ля Рош Аг Новая фармацевтическая композиция, содержащая неионные сурфактанты
TWI765410B (zh) 2014-08-08 2022-05-21 日商中外製藥股份有限公司 4環性化合物的非晶質體的用途

Also Published As

Publication number Publication date
US20190284163A1 (en) 2019-09-19
JP2022153575A (ja) 2022-10-12
JP7116825B2 (ja) 2022-08-10
ES2803577T3 (es) 2021-01-28
JP6906308B2 (ja) 2021-07-21
EP3660009A1 (en) 2020-06-03
TW202222796A (zh) 2022-06-16
US20170217927A1 (en) 2017-08-03
US10344014B2 (en) 2019-07-09
TWI803187B (zh) 2023-05-21
EP3178817B1 (en) 2020-06-10
TW202322823A (zh) 2023-06-16
JP7483804B2 (ja) 2024-05-15
US20230339885A1 (en) 2023-10-26
TWI831347B (zh) 2024-02-01
TWI765410B (zh) 2022-05-21
DK3178817T3 (da) 2020-07-13
EP3178817A4 (en) 2018-01-03
JP2021119194A (ja) 2021-08-12
US20210238160A1 (en) 2021-08-05
EP3178817A1 (en) 2017-06-14
WO2016021707A1 (ja) 2016-02-11
TW201613906A (en) 2016-04-16
US10774067B2 (en) 2020-09-15
TWI718102B (zh) 2021-02-11
TW202115047A (zh) 2021-04-16
JPWO2016021707A1 (ja) 2017-05-25

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