SG11201909735YA - Therapeutic compounds and compositions, and methods of use thereof - Google Patents

Therapeutic compounds and compositions, and methods of use thereof

Info

Publication number
SG11201909735YA
SG11201909735YA SG11201909735YA SG11201909735YA SG 11201909735Y A SG11201909735Y A SG 11201909735YA SG 11201909735Y A SG11201909735Y A SG 11201909735YA SG 11201909735Y A SG11201909735Y A SG 11201909735YA
Authority
SG
Singapore
Prior art keywords
international
pct
methods
designated states
compositions
Prior art date
Application number
Inventor
Mark Zak
F Anthony Romero
Yun-Xing Cheng
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of SG11201909735YA publication Critical patent/SG11201909735YA/en

Links

Classifications

    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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

Abstract

INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 29 November 2018 (29.11.2018) WIPO I PCT mu °mons ono o VI IIIII onll oil Eno iflo oimIE (10) International Publication Number WO 2018/215389 Al (51) International Patent Classification: CO7D 487/04 (2006.01) A61K 31/519 (2006.01) A61P 29/00 (2006.01) TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). (21) International Application Number: (22) International Filing Date: PCT/EP2018/063262 Published: — with international search report (Art. 21(3)) 21 May 2018 (21.05.2018) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: PCT/CN2017/085276 22 May 2017 (22.05.2017) CN 62/640,865 09 March 2018 (09.03.2018) US (71) Applicant (for all designated States except US): F. HOFF- MANN-LA ROCHE AG [CH/CH]; Grenzacherstrasse 124, 4070 Basel (CH). (71) Applicant (for US only): GENENTECH, INC. [US/US]; 1 DNA Way, South San Francisco, California 94080 (US). (72) Inventors: ZAK, Mark; c/o Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080 (US). ROMERO, F. An- thony; 3280 Bayshore Boulevard, Brisbane, CA 94005 (US). CHENG, Yun-Xing; 6 Tai-he Road, BDA, Beijing 100176 (CN). (74) Agent: SCHIRLIN, Julien; Grenzacherstrasse 124, 4070 Basel (CH). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, 1-1 EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, 00 11 el (54) Title: THERAPEUTIC COMPOUNDS AND COMPOSITIONS, AND METHODS OF USE THEREOF (57) : Compounds and salts thereof that are useful as JAK kinse inhibitors are described herein. Also provided are pharma- O ceutical compositions that include such a JAK inhibitor and a pharmaceutically acceptable carrier, adjuvant or vehicle, and methods of \" treating or lessening the severity of a disease or condition responsive to the inhibition of a Janus kinase activity in a patient.
SG11201909735Y 2017-05-22 2018-05-21 Therapeutic compounds and compositions, and methods of use thereof SG11201909735YA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2017085276 2017-05-22
US201862640865P 2018-03-09 2018-03-09
PCT/EP2018/063262 WO2018215389A1 (en) 2017-05-22 2018-05-21 Therapeutic compounds and compositions, and methods of use thereof

Publications (1)

Publication Number Publication Date
SG11201909735YA true SG11201909735YA (en) 2019-11-28

Family

ID=62386421

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201909735Y SG11201909735YA (en) 2017-05-22 2018-05-21 Therapeutic compounds and compositions, and methods of use thereof

Country Status (19)

Country Link
US (3) US10307426B2 (en)
EP (1) EP3630766A1 (en)
JP (2) JP7256757B2 (en)
KR (1) KR20200010390A (en)
CN (1) CN110650959B (en)
AU (1) AU2018274577A1 (en)
BR (1) BR112019024322A2 (en)
CA (1) CA3061236A1 (en)
CL (1) CL2019003258A1 (en)
CO (1) CO2019010559A2 (en)
CR (1) CR20190520A (en)
MA (1) MA48942A (en)
MX (1) MX2019013308A (en)
PE (1) PE20200341A1 (en)
PH (1) PH12019502601A1 (en)
RU (1) RU2769696C2 (en)
SG (1) SG11201909735YA (en)
TW (1) TW201902896A (en)
WO (1) WO2018215389A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2769696C2 (en) * 2017-05-22 2022-04-05 Ф. Хоффманн-Ля Рош Аг Therapeutic compounds and compositions and methods of using them
WO2020188015A1 (en) 2019-03-21 2020-09-24 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
TW202115068A (en) 2019-06-18 2021-04-16 瑞士商赫孚孟拉羅股份公司 Pyrazolopyrimidine sulfone inhibitors of jak kinases and uses thereof
JP2022537354A (en) * 2019-06-18 2022-08-25 エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト Pyrazolopyrimidine aryl ether inhibitors of JAK kinases and uses thereof
WO2021089791A1 (en) 2019-11-08 2021-05-14 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use

Family Cites Families (91)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES517193A0 (en) 1981-11-10 1983-12-01 Wellcome Found A PROCEDURE FOR THE PREPARATION OF NEW IMIDAZO DERIVATIVES (4,5-C) PIRIDINA.
US4847256A (en) 1986-10-16 1989-07-11 American Cyanamid Company 4,5-dihydro and 4,5,6,7-tetrahydropyrazolo(1,5-A)-pyrimidines
AU650953B2 (en) 1991-03-21 1994-07-07 Novartis Ag Inhaler
US5728536A (en) 1993-07-29 1998-03-17 St. Jude Children's Research Hospital Jak kinases and regulation of Cytokine signal transduction
US6136595A (en) 1993-07-29 2000-10-24 St. Jude Children's Research Hospital Jak kinases and regulations of cytokine signal transduction
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
US5705625A (en) 1994-12-15 1998-01-06 The Johns Hopkins University School Of Medicine Nucleic Acid Encoding novel protein tyrosine kinase
US7070972B1 (en) 1995-01-13 2006-07-04 The United States Of America As Represented By The Department Of Health And Human Services Janus family kinases and identification of immune modulators
WO1997002289A1 (en) 1995-07-06 1997-01-23 Zeneca Limited Peptide inhibitors of fibronectine
US6248713B1 (en) 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
US7091020B1 (en) 1995-12-05 2006-08-15 Incyte Corporation Human Jak2 kinase
ID18494A (en) 1996-10-02 1998-04-16 Novartis Ag PIRAZOLA DISTRIBUTION IN THE SEQUENCE AND THE PROCESS OF MAKING IT
US6235741B1 (en) 1997-05-30 2001-05-22 Merck & Co., Inc. Angiogenesis inhibitors
FR2791562B1 (en) 1999-03-29 2004-03-05 Oreal TINCTORIAL COMPOSITION CONTAINING PYRAZOLO- [1,5-A] - PYRIMIDINE AND A MONOCYCLIC POLYAMINOPYRIMIDINE AS OXIDATION BASES AND A COUPLER, AND DYEING METHODS
YU25500A (en) 1999-05-11 2003-08-29 Pfizer Products Inc. Process for the synthesis of nucleosite analogues
EP1221444B1 (en) 1999-07-02 2005-08-31 Eisai Co., Ltd. Fused imidazole compounds and remedies for diabetes mellitus
CZ303875B6 (en) 1999-12-10 2013-06-05 Pfizer Products Inc. Pyrrolo [2,3-d]pyrimidine compound and pharmaceutical composition in which the compound is comprised
GB0028383D0 (en) 2000-11-21 2001-01-03 Novartis Ag Organic compounds
EP1241176A1 (en) 2001-03-16 2002-09-18 Pfizer Products Inc. Purine derivatives for the treatment of ischemia
EP1458682B1 (en) 2001-12-20 2006-08-30 Bayer HealthCare AG 1,4-dihydro-1,4-diphenylpyridine derivatives
CN100343255C (en) 2002-04-23 2007-10-17 盐野义制药株式会社 Pyrazolo (1,5-a) pyrimidine derivative and nad(p)h oxidase inhibitor containing the same
US7161003B1 (en) 2002-09-04 2007-01-09 Schering Corporation Pyrazolopyrimidines as cyclin dependent kinase inhibitors
US8580782B2 (en) 2002-09-04 2013-11-12 Merck Sharp & Dohme Corp. Substituted pyrazolo[1,5-a]pyrimidines as cyclin dependent kinase inhibitors
US7129239B2 (en) 2002-10-28 2006-10-31 Pfizer Inc. Purine compounds and uses thereof
AU2003270701B2 (en) 2002-10-31 2009-11-12 Amgen Inc. Antiinflammation agents
US7550470B2 (en) 2002-12-11 2009-06-23 Merck & Co. Inc. Substituted pyrazolo[1,5-A]pyrimidines as tyrosine kinase inhibitors
US20070270408A1 (en) 2003-04-11 2007-11-22 Novo Nordisk A/S Pharmaceutical use of substituted pyrazolo[1,5-a]pyrimidines
WO2004089471A2 (en) 2003-04-11 2004-10-21 Novo Nordisk A/S NEW PYRAZOLO[1,5-a] PYRIMIDINES DERIVATIVES AND PHARMACEUTICAL USE THEREOF
WO2004089416A2 (en) 2003-04-11 2004-10-21 Novo Nordisk A/S Combination of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent
WO2004089415A2 (en) 2003-04-11 2004-10-21 Novo Nordisk A/S COMBINATIONS OF AN 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND A GLUCOCORTICOID RECEPTOR AGONIST
US7393873B2 (en) 2003-07-02 2008-07-01 Merck & Co., Inc. Arylsulfonamide derivatives
TWI372050B (en) 2003-07-03 2012-09-11 Astex Therapeutics Ltd (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles
SE0302487D0 (en) 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
GB0329214D0 (en) 2003-12-17 2004-01-21 Glaxo Group Ltd Novel compounds
US7306631B2 (en) 2004-03-30 2007-12-11 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
CA2563305A1 (en) 2004-04-09 2005-11-24 University Of South Florida Combination therapies for cancer and proliferative angiopathies
JP2007535560A (en) 2004-04-28 2007-12-06 シーブイ・セラピューティクス・インコーポレイテッド A1 adenosine receptor antagonist
MXPA06014637A (en) 2004-06-25 2007-02-12 Amgen Inc Condensed triazoles and indazoles useful in treating citokines mediated diseases and other diseases.
NZ555236A (en) 2004-11-04 2010-10-29 Vertex Pharma Pyrazolo[1,5-a]pyrimidines useful as inhibitors of protein kinases
GB0502258D0 (en) 2005-02-03 2005-03-09 Argenta Discovery Ltd Compounds and their use
JP2009502734A (en) 2005-07-29 2009-01-29 アステラス製薬株式会社 Fused heterocycles as Lck inhibitors
WO2007039797A1 (en) 2005-10-03 2007-04-12 Pfizer Products Inc. Use of cannabinoid receptor-1 antagonist for treating inflammation and arthritis
CA2624500A1 (en) 2005-10-06 2007-04-19 Schering Corporation Pyrazolopyrimidines as protein kinase inhibitors
US7776865B2 (en) * 2005-10-06 2010-08-17 Schering Corporation Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors
CA2626742A1 (en) 2005-10-21 2007-04-26 Exelixis, Inc. Pyrazolo-pyrimidines as casein kinase ii (ck2) modulators
WO2007065664A2 (en) 2005-12-08 2007-06-14 Novartis Ag Pyrazolo[1,5-a]pyridine-3-carboxylic acids as ephb and vegfr2 kinase inhibitors
US8541406B2 (en) 2006-02-07 2013-09-24 Nv Remynd Thiadiazole derivatives for the treatment of neurodegenerative diseases
TW200800997A (en) 2006-03-22 2008-01-01 Astrazeneca Ab Chemical compounds
AR061793A1 (en) 2006-07-05 2008-09-24 Mitsubishi Tanabe Pharma Corp PIRAZOLO COMPOUND [1,5-A] PYRIMIDINE AND PHARMACEUTICAL COMPOSITION
PE20080403A1 (en) 2006-07-14 2008-04-25 Amgen Inc FUSED HETEROCYCLIC DERIVATIVES AND METHODS OF USE
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
MX2009004715A (en) 2006-10-30 2009-05-20 Novartis Ag Heterocyclic compounds as antiinflammatory agents.
US20080176870A1 (en) 2006-11-20 2008-07-24 Bert Nolte Heterobicyclic metalloprotease inhibitors
WO2009017954A1 (en) 2007-08-01 2009-02-05 Phenomix Corporation Inhibitors of jak2 kinase
EP2212297B1 (en) 2007-10-12 2011-05-25 Ingenium Pharmaceuticals GmbH Inhibitors of protein kinases
CA2707046A1 (en) 2007-11-28 2009-06-11 Nathanael S. Gray Small molecule myristate inhibitors of bcr-abl and methods of use
US8642660B2 (en) 2007-12-21 2014-02-04 The University Of Rochester Method for altering the lifespan of eukaryotic organisms
CA2727036C (en) 2008-06-20 2017-03-21 Genentech, Inc. Triazolopyridine jak inhibitor compounds and methods
WO2010019762A1 (en) 2008-08-13 2010-02-18 Jenrin Discovery Purine compounds as cannabinoid receptor blockers
AU2009308675A1 (en) * 2008-10-31 2010-05-06 Genentech, Inc. Pyrazolopyrimidine JAK inhibitor compounds and methods
WO2010063487A1 (en) 2008-12-05 2010-06-10 Merz Pharma Gmbh & Co. Kgaa Pyrazolopyrimidines, a process for their preparation and their use as medicine
CN102325765B (en) 2009-02-06 2014-12-24 杨森制药公司 Novel substituted bicyclic heterocyclic compounds as gamma secretase modulators
TWI461425B (en) 2009-02-19 2014-11-21 Janssen Pharmaceuticals Inc Novel substituted benzoxazole, benzimidazole, oxazolopyridine and imidazopyridine derivatives as gamma secretase modulators
UA110324C2 (en) 2009-07-02 2015-12-25 Genentech Inc Jak inhibitory compounds based on pyrazolo pyrimidine
AR077468A1 (en) 2009-07-09 2011-08-31 Array Biopharma Inc PIRAZOLO COMPOUNDS (1,5-A) PYRIMIDINE SUBSTITUTED AS TRK-QUINASA INHIBITORS
CN102666545B (en) 2009-10-20 2016-04-06 塞尔卓姆有限公司 As the heterocycle Pyrazolopyrimidine analogs of JAK inhibitor
CA2793024A1 (en) 2010-03-17 2011-09-22 F. Hoffmann-La Roche Ag Imidazopyridine compounds, compositions and methods of use
EA201291038A1 (en) 2010-04-30 2013-05-30 Целльзом Лимитид PYRAZOL COMPOUNDS AS JAK INHIBITORS
JP5985473B2 (en) 2010-07-13 2016-09-06 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Pyrazolo [1,5a] pyrimidine and thieno [3,2b] pyrimidine derivatives as IRAK4 modulators
WO2012075393A2 (en) 2010-12-02 2012-06-07 President And Fellows Of Harvard College Activators of proteasomal degradation and uses thereof
WO2012129258A1 (en) 2011-03-22 2012-09-27 Merck Sharp & Dohme Corp. Amidopyrazole inhibitors of interleukin receptor-associated kinases
US8575336B2 (en) 2011-07-27 2013-11-05 Pfizer Limited Indazoles
EP2892899B1 (en) 2012-09-06 2018-03-21 Bristol-Myers Squibb Company Imidazopyridazine jak3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
SG11201503517WA (en) 2012-11-09 2015-06-29 Jacobus Pharmaceutical Company Inc Heteroaryl derivatives and uses thereof
EP3019171B1 (en) 2013-07-11 2018-09-05 Merck Sharp & Dohme Corp. Substituted amidopyrazole inhibitors of interleukin receptor-associated kinases (irak-4)
EA201690952A1 (en) 2013-11-08 2016-08-31 Такеда Фармасьютикал Компани Лимитед PYRAZOL FOR THE TREATMENT OF AUTOIMMUNE DISORDERS
WO2015073267A1 (en) 2013-11-15 2015-05-21 Calitor Sciences, Llc Substituted heteroaryl compounds and methods of use
EP3145522B1 (en) 2014-05-23 2020-12-23 Phibro Animal Health Corporation Combination, composition, and method of administering the combination or composition to animals
JO3701B1 (en) 2014-05-23 2021-01-31 Regeneron Pharma Human antibodies to middle east respiratory syndrome – coronavirus spike protein
US9346815B2 (en) 2014-05-23 2016-05-24 Genentech, Inc. 5-chloro-2-difluoromethoxyphenyl pyrazolopyrimidine compounds, compositions and methods of use thereof
CN107001379B (en) 2014-11-06 2022-11-01 Bial研发投资股份有限公司 Substituted pyrazolo [1,5-a ] pyrimidines and their use in the treatment of medical disorders
WO2016144846A1 (en) 2015-03-12 2016-09-15 Merck Sharp & Dohme Corp. Pyrazolopyrimidine inhibitors of irak4 activity
WO2016144844A1 (en) 2015-03-12 2016-09-15 Merck Sharp & Dohme Corp. Carboxamide inhibitors of irak4 activity
EP3268004B1 (en) 2015-03-12 2019-12-18 Merck Sharp & Dohme Corp. Pyrrolopyridazine inhibitors of irak4 activity
WO2016144848A1 (en) 2015-03-12 2016-09-15 Merck Sharp & Dohme Corp. Pyrrolotriazine inhibitors of irak4 activity
TW201720828A (en) 2015-11-23 2017-06-16 赫孚孟拉羅股份公司 Therapeutic compounds and compositions, and methods of use thereof
WO2017140825A1 (en) 2016-02-18 2017-08-24 F. Hoffmann-La Roche Ag Therapeutic compounds, compositions and methods of use thereof
CR20190310A (en) 2016-12-29 2019-08-21 Hoffmann La Roche Pyrazolopyrimidine compounds and methods of use thereof
WO2018166993A2 (en) 2017-03-14 2018-09-20 F. Hoffmann-La Roche Ag Pyrazolochlorophenyl compounds, compositions and methods of use thereof
EP3630767A1 (en) 2017-05-22 2020-04-08 H. Hoffnabb-La Roche Ag Therapeutic compounds and compositions, and methods of use thereof
RU2769696C2 (en) * 2017-05-22 2022-04-05 Ф. Хоффманн-Ля Рош Аг Therapeutic compounds and compositions and methods of using them

Also Published As

Publication number Publication date
TW201902896A (en) 2019-01-16
BR112019024322A2 (en) 2020-06-16
JP2020520959A (en) 2020-07-16
CN110650959B (en) 2023-04-18
PE20200341A1 (en) 2020-02-14
EP3630766A1 (en) 2020-04-08
RU2019141734A3 (en) 2021-08-10
CR20190520A (en) 2020-01-21
MX2019013308A (en) 2020-02-12
US10307426B2 (en) 2019-06-04
CA3061236A1 (en) 2018-11-29
CO2019010559A2 (en) 2019-10-09
PH12019502601A1 (en) 2020-06-08
KR20200010390A (en) 2020-01-30
MA48942A (en) 2020-04-08
US20190240227A1 (en) 2019-08-08
CL2019003258A1 (en) 2020-04-17
JP2023058657A (en) 2023-04-25
AU2018274577A1 (en) 2019-10-10
RU2769696C2 (en) 2022-04-05
CN110650959A (en) 2020-01-03
RU2019141734A (en) 2021-06-23
US20200352951A1 (en) 2020-11-12
WO2018215389A1 (en) 2018-11-29
JP7256757B2 (en) 2023-04-12
US20180333416A1 (en) 2018-11-22

Similar Documents

Publication Publication Date Title
SG11201909735YA (en) Therapeutic compounds and compositions, and methods of use thereof
SG11201806863WA (en) Tetracyclic pyridone compounds as antivirals
SG11201805044WA (en) Compounds useful as kinase inhibitors
SG11201811470PA (en) Pyrazolopyrimidine derivatives as kinase inhibitor
SG11201908670SA (en) Pyrrolopyrrole compositions as pyruvate kinase (pkr) activators
SG11201810423XA (en) Pd-1 / pd-l1 inhibitors for cancer treatment
SG11201803920TA (en) Compounds and compositions useful for treating disorders related to ntrk
SG11201808878UA (en) Heterocyclic compounds as ret kinase inhibitors
SG11201808990QA (en) Compositions for topical application of compounds
SG11201808222RA (en) Methods of treatment of cholestatic diseases
SG11201810280YA (en) Spiro-lactam nmda receptor modulators and uses thereof
SG11201808237UA (en) Substituted indole compound derivatives as dengue viral replication inhibitors
SG11201407200TA (en) Liquid formulation
SG11201908517XA (en) Pyrimidinyl-pyridyloxy-naphthyl compounds and methods of treating ire1-related diseases and disorders
SG11201808106YA (en) Use of masitinib for treatment of an amyotrophic lateral sclerosis patient subpopulation
SG11202000333UA (en) Bicyclic ketone compounds and methods of use thereof
SG11201901534VA (en) Combination therapy with controlled-release cnp agonists
SG11201900558RA (en) Spiro-lactam nmda receptor modulators and uses thereof
SG11201407988UA (en) Process for improved opioid synthesis
SG11201806544XA (en) Compounds and methods of treating rna-mediated diseases
SG11201808713YA (en) Ophthalmic compositions comprising levodopa, an antioxidant and an aqueous carrier
SG11201901063SA (en) Therapeutic agents for neurodegenerative diseases
SG11201901689YA (en) Compounds for treating diseases associated with a mitochondrial dysfonction
SG11201901048VA (en) Pharmaceutical compositions and uses directed to lysosomal storage disorders
SG11201809764XA (en) Humanized anti-il-1r3 antibodies