SG10202101389TA - Crystalline forms of a bruton’s tyrosine kinase inhibitor - Google Patents

Crystalline forms of a bruton’s tyrosine kinase inhibitor

Info

Publication number
SG10202101389TA
SG10202101389TA SG10202101389TA SG10202101389TA SG10202101389TA SG 10202101389T A SG10202101389T A SG 10202101389TA SG 10202101389T A SG10202101389T A SG 10202101389TA SG 10202101389T A SG10202101389T A SG 10202101389TA SG 10202101389T A SG10202101389T A SG 10202101389TA
Authority
SG
Singapore
Prior art keywords
bruton
tyrosine kinase
kinase inhibitor
crystalline forms
crystalline
Prior art date
Application number
SG10202101389TA
Other languages
English (en)
Inventor
Mark Smyth
Erick Goldman
David Wirth
Norbert Purro
Original Assignee
Pharmacyclics Llc
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=49712527&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG10202101389T(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pharmacyclics Llc filed Critical Pharmacyclics Llc
Publication of SG10202101389TA publication Critical patent/SG10202101389TA/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
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    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
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    • 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
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    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
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    • 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
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
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    • C07B2200/13Crystalline forms, e.g. polymorphs

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  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Reproductive Health (AREA)
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  • Otolaryngology (AREA)
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  • Pain & Pain Management (AREA)
  • Mechanical Engineering (AREA)
  • Composite Materials (AREA)
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  • Inorganic Chemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Ophthalmology & Optometry (AREA)
SG10202101389TA 2012-06-04 2013-06-03 Crystalline forms of a bruton’s tyrosine kinase inhibitor SG10202101389TA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261655381P 2012-06-04 2012-06-04

Publications (1)

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SG10202101389TA true SG10202101389TA (en) 2021-03-30

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SG11201408067YA SG11201408067YA (en) 2012-06-04 2013-06-03 Crystalline forms of a bruton's tyrosine kinase inhibitor
SG10202101389TA SG10202101389TA (en) 2012-06-04 2013-06-03 Crystalline forms of a bruton’s tyrosine kinase inhibitor

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Country Status (32)

Country Link
US (25) US9296753B2 (he)
EP (1) EP2854859A4 (he)
JP (8) JP6236071B2 (he)
KR (7) KR20190040370A (he)
CN (2) CN104736178A (he)
AR (2) AR092844A1 (he)
AU (6) AU2013271918C1 (he)
BR (1) BR112014030424A8 (he)
CA (4) CA2991994C (he)
CL (3) CL2014003306A1 (he)
CO (1) CO7240408A2 (he)
CR (1) CR20140558A (he)
DO (3) DOP2014000274A (he)
EA (1) EA201492082A1 (he)
EC (2) ECSP14033163A (he)
GT (1) GT201400281A (he)
HK (1) HK1208803A1 (he)
IL (3) IL235894B (he)
JO (2) JO3754B1 (he)
MA (2) MA41654B2 (he)
MX (2) MX348290B (he)
MY (2) MY187999A (he)
NZ (4) NZ737725A (he)
PE (3) PE20150174A1 (he)
PH (2) PH12014502681A1 (he)
SG (2) SG11201408067YA (he)
TN (1) TN2014000492A1 (he)
TW (3) TWI662964B (he)
UA (2) UA114421C2 (he)
UY (2) UY39740A (he)
WO (1) WO2013184572A1 (he)
ZA (3) ZA202105175B (he)

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EP2201840B1 (en) 2006-09-22 2011-11-02 Pharmacyclics, Inc. Inhibitors of Bruton's Tyrosine Kinase
US20120101114A1 (en) 2007-03-28 2012-04-26 Pharmacyclics, Inc. Inhibitors of bruton's tyrosine kinase
EP2307025B1 (en) 2008-07-16 2017-09-20 Pharmacyclics LLC Inhibitors of bruton's tyrosine kinase for the treatment of solid tumors
US8491927B2 (en) * 2009-12-02 2013-07-23 Nimble Epitech, Llc Pharmaceutical composition containing a hypomethylating agent and a histone deacetylase inhibitor
CA3113343A1 (en) 2010-06-03 2011-12-08 Pharmacyclics Llc Use of inhibitors of bruton's tyrosine kinase (btk) in the treatment of follicular lymphoma
SG10201600077RA (en) 2011-01-11 2016-02-26 Glaxosmithkline Llc Combination
AU2012283775A1 (en) 2011-07-13 2014-01-23 Pharmacyclics Llc Inhibitors of Bruton's tyrosine kinase
WO2013013188A1 (en) 2011-07-21 2013-01-24 Tolero Pharmaceuticals, Inc. Heterocyclic protein kinase inhibitors
EP2788343B1 (en) 2011-12-11 2018-02-28 Viamet Pharmaceuticals (NC), Inc. Metalloenzyme inhibitor compounds
US8377946B1 (en) 2011-12-30 2013-02-19 Pharmacyclics, Inc. Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors
KR20190040370A (ko) * 2012-06-04 2019-04-17 파마싸이클릭스 엘엘씨 브루톤 타이로신 키나아제 저해제의 결정 형태
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CL2017000371A1 (es) 2017-10-30
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EP2854859A1 (en) 2015-04-08
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CN104736178A (zh) 2015-06-24
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JOP20200222A1 (ar) 2022-10-30
EA201492082A1 (ru) 2015-03-31
AR118108A2 (es) 2021-09-15
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MA41654A1 (fr) 2018-07-31
US9540382B2 (en) 2017-01-10
AU2013271918A1 (en) 2015-01-22
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PE20150174A1 (es) 2015-02-12
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CR20140558A (es) 2015-03-13

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