EA028434B1 - Лечение рака ингибиторами tor киназы - Google Patents

Лечение рака ингибиторами tor киназы Download PDF

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Publication number
EA028434B1
EA028434B1 EA201491694A EA201491694A EA028434B1 EA 028434 B1 EA028434 B1 EA 028434B1 EA 201491694 A EA201491694 A EA 201491694A EA 201491694 A EA201491694 A EA 201491694A EA 028434 B1 EA028434 B1 EA 028434B1
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Eurasian Patent Office
Prior art keywords
overexpression
patient
twenty
stereoisomer
ethyl
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EA201491694A
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English (en)
Russian (ru)
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EA201491694A1 (ru
Inventor
Шуйчань Сюй
Кристен Мей Хедж
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СИГНАЛ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи
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Publication of EA201491694A1 publication Critical patent/EA201491694A1/ru
Publication of EA028434B1 publication Critical patent/EA028434B1/ru

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    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
    • 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
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/57407Specifically defined cancers

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Cell Biology (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Hospice & Palliative Care (AREA)
  • Food Science & Technology (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
EA201491694A 2012-03-15 2013-03-14 Лечение рака ингибиторами tor киназы EA028434B1 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261611370P 2012-03-15 2012-03-15
US201261715329P 2012-10-18 2012-10-18
PCT/US2013/031202 WO2013138556A1 (en) 2012-03-15 2013-03-14 Treatment of cancer with tor kinase inhibitors

Publications (2)

Publication Number Publication Date
EA201491694A1 EA201491694A1 (ru) 2015-06-30
EA028434B1 true EA028434B1 (ru) 2017-11-30

Family

ID=47998542

Family Applications (1)

Application Number Title Priority Date Filing Date
EA201491694A EA028434B1 (ru) 2012-03-15 2013-03-14 Лечение рака ингибиторами tor киназы

Country Status (20)

Country Link
US (1) US20130245029A1 (OSRAM)
EP (1) EP2825168B1 (OSRAM)
JP (2) JP2015516375A (OSRAM)
KR (3) KR102057358B1 (OSRAM)
CN (2) CN104302295B (OSRAM)
AU (1) AU2013203156C1 (OSRAM)
BR (1) BR112014022697A2 (OSRAM)
CA (1) CA2867349A1 (OSRAM)
EA (1) EA028434B1 (OSRAM)
ES (1) ES2677908T3 (OSRAM)
IL (2) IL234640B (OSRAM)
MX (1) MX360877B (OSRAM)
MY (1) MY182650A (OSRAM)
NI (1) NI201400109A (OSRAM)
NZ (1) NZ628421A (OSRAM)
PH (2) PH12014502048B1 (OSRAM)
SG (1) SG11201405706TA (OSRAM)
TW (2) TWI600428B (OSRAM)
WO (1) WO2013138556A1 (OSRAM)
ZA (1) ZA201406709B (OSRAM)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2013203714B2 (en) 2012-10-18 2015-12-03 Signal Pharmaceuticals, Llc Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity
CN105188704B (zh) 2013-01-16 2017-09-19 西格诺药品有限公司 被取代的吡咯并嘧啶化合物、其组合物和使用其的治疗方法
KR102221029B1 (ko) 2013-04-17 2021-02-26 시그날 파마소티칼 엘엘씨 디하이드로피라지노-피라진을 사용한 암의 치료
UA115805C2 (uk) 2013-04-17 2017-12-26 Сігнал Фармасьютікалз, Елелсі Комбінована терапія, яка включає сполуку дигідропіразинопіразину й антагоніст рецептора андрогену, для лікування раку простати
US9358232B2 (en) 2013-04-17 2016-06-07 Signal Pharmaceuticals, Llc Methods for treating cancer using TOR kinase inhibitor combination therapy
PH12021552945B1 (en) 2013-04-17 2024-02-28 Signal Pharm Llc Treatment of cancer with dihydropyrazino-pyrazines
WO2014172436A1 (en) 2013-04-17 2014-10-23 Signal Pharmaceuticals, Llc Combination therapy comprising a tor kinase inhibitor and a 5-substituted quinazolinone compound for treating cancer
EA037683B1 (ru) 2013-04-17 2021-04-29 СИГНАЛ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи Фармацевтические составы, способы, твердые формы и способы применения, относящиеся к 1-этил-7-(2-метил-6-(1h-1,2,4-триазол-3-ил)пиридин-3-ил)-3,4-дигидропиразино[2,3-b] пиразин-2(1h)-ону
NZ631082A (en) 2013-04-17 2017-06-30 Signal Pharm Llc Methods for treating cancer using tor kinase inhibitor combination therapy
CN105407892B (zh) 2013-05-29 2019-05-07 西格诺药品有限公司 一种化合物的药物组合物、其固体形式及它们的使用方法
NZ714742A (en) 2014-04-16 2017-04-28 Signal Pharm Llc Solid forms of 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, compositions thereof and methods of their use
WO2015160882A1 (en) 2014-04-16 2015-10-22 Signal Pharmaceuticals, Llc SOLID FORMS COMPRISING 7-(6-(2-HYDROXYPROPAN-2YL) PYRIDIN-3-YL)-1-(TRANS)-4-METHOXYCYCLOHEXYL)-3, 4-DIHYDROPYRAZINO[2,3-b] PYRAZIN-2(1H)-ONE, AND A COFORMER, COMPOSITIONS AND METHODS OF USE THEREOF
WO2015160868A1 (en) 2014-04-16 2015-10-22 Signal Pharmaceuticals, Llc Methods for treating cancer using tor kinase inhibitor combination therapy
WO2015160880A1 (en) 2014-04-16 2015-10-22 Signal Pharmaceuticals, Llc SOLID FORMS COMPRISING 1-ETHYL-7-(2-METHYL-6-(1H-1,2,4-TRIAZOL-3-YL) PYRIDIN-3-YL)-3,4-DIHYDROPYRAZINO(2,3-b)PYRAZIN-2(1H)-ONE, AND A COFORMER, COMPOSITIONS AND METHODS OF USE THEREOF
NZ629796A (en) 2014-07-14 2015-12-24 Signal Pharm Llc Amorphous form of 4-((4-(cyclopentyloxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7h-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-3-methoxy-n-methylbenzamide, compositions thereof and methods of their use
CA2955009A1 (en) 2014-07-14 2016-01-21 Signal Pharmaceuticals, Llc Methods of treating a cancer using substituted pyrrolopyrimidine compounds, compositions thereof
AU2017384388B2 (en) * 2016-12-20 2020-09-17 Astrazeneca Ab Amino-triazolopyridine compounds and their use in treating cancer
IL271491B2 (en) 2017-06-22 2023-09-01 Celgene Corp Treatment of carcinoma of the liver characterized by hepatitis b virus infection
SG11202008010SA (en) * 2018-03-01 2020-09-29 Essilor Int Lens element
CN113493471B (zh) * 2020-04-03 2024-06-11 山东轩竹医药科技有限公司 杂芳环类激酶抑制剂

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008051494A1 (en) * 2006-10-19 2008-05-02 Signal Pharmaceuticals, Llc Heteroaryl compounds, compositions thereof, and use thereof as protein kinase inhibitors
WO2008051493A2 (en) * 2006-10-19 2008-05-02 Signal Pharmaceuticals, Llc Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors
WO2010062571A1 (en) * 2008-10-27 2010-06-03 Signal Pharmaceuticals, Llc Mtor kinase inhibitors for oncology indications and diseases associated with the mtor/p13k/akt pathway
WO2011133668A2 (en) * 2010-04-20 2011-10-27 President And Fellows Of Harvard College Methods and compositions for the treatment of cancer

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ599549A (en) 2009-10-26 2013-11-29 Signal Pharm Llc Methods of synthesis and purification of heteroaryl compounds

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008051494A1 (en) * 2006-10-19 2008-05-02 Signal Pharmaceuticals, Llc Heteroaryl compounds, compositions thereof, and use thereof as protein kinase inhibitors
WO2008051493A2 (en) * 2006-10-19 2008-05-02 Signal Pharmaceuticals, Llc Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors
WO2010062571A1 (en) * 2008-10-27 2010-06-03 Signal Pharmaceuticals, Llc Mtor kinase inhibitors for oncology indications and diseases associated with the mtor/p13k/akt pathway
WO2011133668A2 (en) * 2010-04-20 2011-10-27 President And Fellows Of Harvard College Methods and compositions for the treatment of cancer

Non-Patent Citations (12)

* Cited by examiner, † Cited by third party
Title
ANA S. MARTINS, ET AL.: "Insulin-Like Growth Factor IReceptor Pathway Inhibition byADW742, Alone or in Combinationwith Imatinib,Doxorubicin, orVincristine, Is a Novel Therapeutic Approach in EwingTumor", CLINICAL CANCER RESEARCH, THE AMERICAN ASSOCIATION FOR CANCER RESEARCH., US, vol. 12, no. 11, 1 June 2006 (2006-06-01), US, pages 3532 - 3540, XP002551195, ISSN: 1078-0432, DOI: 10.1158/1078-0432.CCR-05-1778 *
BALAMUTH, N.J. ; WOMER, R.B.: "Ewing's sarcoma", THE LANCET ONCOLOGY, ELSEVIER, AMSTERDAM, NL, vol. 11, no. 2, 1 February 2010 (2010-02-01), AMSTERDAM, NL, pages 184 - 192, XP026884321, ISSN: 1470-2045, DOI: 10.1016/S1470-2045(09)70286-4 *
DANCEY JANET E; MONZON JOSE: "Ridaforolimus: a promising drug in the treatment of soft-tissue sarcoma and other malignancies", FUTURE ONCOLOGY, UK, vol. 7, no. 7, 1 July 2011 (2011-07-01), UK, pages 827 - 839, XP009169333, ISSN: 1744-8301, DOI: 10.2217/fon.11.57 *
LORI BERK; MONICA M. MITA; JEFF KREISBERG; CAMILLE L. BEDROSIAN; ANTHONY W. TOLCHER; TIM CLACKSON; VICTOR M. RIVERA: "Analysis of the pharmacodynamic activity of the mTOR inhibitor ridaforolimus (AP23573, MK-8669) in a phase 1 clinical trial", CANCER CHEMOTHERAPY AND PHARMACOLOGY, SPRINGER, BERLIN, DE, vol. 69, no. 5, 10 January 2012 (2012-01-10), Berlin, DE, pages 1369 - 1377, XP035047366, ISSN: 1432-0843, DOI: 10.1007/s00280-011-1813-7 *
MARK AGULNIK: "New developments in mammalian target of rapamycin inhibitors for the treatment of sarcoma", CANCER, ¬JOHN WILEY & SONS| :, vol. 118, no. 6, 15 March 2012 (2012-03-15), pages 1486 - 1497, XP055061618, ISSN: 0008543X, DOI: 10.1002/cncr.26361 *
MITA M M, MITA A C, CHU Q S, ROWINSKY E K, FETTERLY G J, GOLDSTON M, PATNAIK A, MATHEWS L, RICART A D, MAYS T, KNOWLES H, RIVERA V: "Phase I trial of the novel mammalian target of rapamycin inhibitor deforolimus (AP23573; MK-8669) administered intravenously daily for 5 days every 2 weeks to patients with advanced malignancies.", JOURNAL OF CLINICAL ONCOLOGY, LIPPINCOTT WILLIAMS & WILKINS, USA, vol. 26, no. 3, 20 January 2008 (2008-01-20), USA, pages 361 - 367, XP002696908, ISSN: 1527-7755, DOI: 10.1200/JCO.2007.12.0345 *
OIKAWA T: "ETS TRANSCRIPTION FACTORS: POSSIBLE TARGETS FOR CANCER THERAPY", CANCER SCIENCE, JAPANESE CANCER ASSOCIATION, TOKYO, JP, vol. 95, no. 08, 1 August 2004 (2004-08-01), JP, pages 626 - 633, XP009039358, ISSN: 1347-9032, DOI: 10.1111/j.1349-7006.2004.tb03320.x *
P. C. HOLLENHORST, M. W. FERRIS, M. A. HULL, H. CHAE, S. KIM, B. J. GRAVES: "Oncogenic ETS proteins mimic activated RAS/MAPK signaling in prostate cells", GENES & DEVELOPMENT, COLD SPRING HARBOR LABORATORY PRESS, vol. 25, no. 20, 15 October 2011 (2011-10-15), pages 2147 - 2157, XP055061642, ISSN: 08909369, DOI: 10.1101/gad.17546311 *
R. M. SQUILLACE, D. MILLER, M. COOKSON, S. D. WARDWELL, L. MORAN, D. CLAPHAM, F. WANG, T. CLACKSON, V. M. RIVERA: "Antitumor Activity of Ridaforolimus and Potential Cell-Cycle Determinants of Sensitivity in Sarcoma and Endometrial Cancer Models", MOLECULAR CANCER THERAPEUTICS, AMERICAN ASSOCIATION FOR CANCER RESEARCH, INC., vol. 10, no. 10, 1 October 2011 (2011-10-01), pages 1959 - 1968, XP055061614, ISSN: 15357163, DOI: 10.1158/1535-7163.MCT-11-0273 *
SILVIA MATEO-LOZANO, OSCAR M TIRADO AND VICENTE NOTARIO: "Rapamycin induces the fusion-type independent downregulation of the EWS/FLI-1 proteins and inhibits Ewing's sarcoma cell proliferation.", ONCOGENE, vol. 22, no. 58, 18 December 2003 (2003-12-18), pages 9282 - 9287, XP002665931, ISSN: 0950-9232, DOI: 10.1038/SJ.ONC.1207081 *
VINCENZI BRUNO; NAPOLITANO ANDREA; D'ONOFRIO LORETTA; FREZZA ANNA MARIA; SILLETTA MARIANNA; VENDITTI OLGA; SANTINI DANIELE; TONINI: "Targeted therapy in sarcomas: mammalian target of rapamycin inhibitors from bench to bedside", EXPERT OPINION ON INVESTIGATIONAL DRUGS, INFORMA HEALTHCARE, UNITED KINGDOM, vol. 20, no. 12, 1 December 2011 (2011-12-01), United Kingdom, pages 1685 - 1705, XP009169335, ISSN: 1744-7658, DOI: 10.1517/13543784.2011.628984 *
VIVEK SUBBIAH, AUNG NAING, ROBERT E. BROWN, HELEN CHEN, LAURENCE DOYLE, PATRICIA LORUSSO, ROBERT BENJAMIN, PETE ANDERSON, RAZELLE : "Targeted Morphoproteomic Profiling of Ewing's Sarcoma Treated with Insulin-Like Growth Factor 1 Receptor (IGF1R) Inhibitors: Response/Resistance Signatures", PLOS ONE, PUBLIC LIBRARY OF SCIENCE, vol. 6, no. 4, 1 January 2011 (2011-01-01), pages e18424 - e18424, XP055061616, ISSN: 19326203, DOI: 10.1371/journal.pone.0018424 *

Also Published As

Publication number Publication date
AU2013203156B2 (en) 2015-12-10
MY182650A (en) 2021-01-27
CN107137402A (zh) 2017-09-08
NZ628421A (en) 2016-04-29
AU2013203156C1 (en) 2016-02-18
TW201343167A (zh) 2013-11-01
PH12018502234A1 (en) 2019-08-14
ES2677908T3 (es) 2018-08-07
US20130245029A1 (en) 2013-09-19
EA201491694A1 (ru) 2015-06-30
IL234640A0 (en) 2014-11-30
TW201733586A (zh) 2017-10-01
JP2015516375A (ja) 2015-06-11
NI201400109A (es) 2015-01-15
ZA201406709B (en) 2016-07-27
CN104302295A (zh) 2015-01-21
JP6470821B2 (ja) 2019-02-13
AU2013203156A1 (en) 2013-10-03
PH12018502234B1 (en) 2021-07-23
MX2014011117A (es) 2015-04-08
IL234640B (en) 2020-05-31
TWI664968B (zh) 2019-07-11
TWI600428B (zh) 2017-10-01
KR20140138929A (ko) 2014-12-04
SG11201405706TA (en) 2014-10-30
WO2013138556A1 (en) 2013-09-19
BR112014022697A2 (pt) 2020-06-30
CA2867349A1 (en) 2013-09-19
CN104302295B (zh) 2017-06-20
KR20190058673A (ko) 2019-05-29
EP2825168A1 (en) 2015-01-21
PH12014502048A1 (en) 2014-12-10
PH12014502048B1 (en) 2020-10-28
KR102057358B1 (ko) 2019-12-18
MX360877B (es) 2018-11-21
EP2825168B1 (en) 2018-05-09
HK1201755A1 (en) 2015-09-11
IL274318A (en) 2020-06-30
JP2018065820A (ja) 2018-04-26
KR20200034818A (ko) 2020-03-31

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