HRP20230362T1 - Kompozicije koje sadrže triciklične heterorociklične spojeve - Google Patents

Kompozicije koje sadrže triciklične heterorociklične spojeve Download PDF

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HRP20230362T1
HRP20230362T1 HRP20230362TT HRP20230362T HRP20230362T1 HR P20230362 T1 HRP20230362 T1 HR P20230362T1 HR P20230362T T HRP20230362T T HR P20230362TT HR P20230362 T HRP20230362 T HR P20230362T HR P20230362 T1 HRP20230362 T1 HR P20230362T1
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Stephen Joseph Shuttleworth
Alexander Richard Liam Cecil
Elizabeth Ann Bone
Franck Alexandre Silva
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Convalife (Shanghai) Co. Limited
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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
    • A61K31/535Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • A61K9/2018Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
    • 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
    • A61K31/535Heterocyclic 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
    • A61K31/53861,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/2027Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2095Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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]
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Transplantation (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Claims (18)

1. Farmaceutski sastav koji sadrži spoj formule I u obliku njegove sukcinantne soli, i najmanje jedno farmaceutsko pomoćno sredstvo koje je izabrano iz grupe koja čine punila, vezivna sredstva, dezintegranti, sredstva za klizanje i lubrikanti, pri čemu je spoj prema formuli I predstavljen: [image] pri čemu: W je O, N-H, N-(C1-C10 alkil) ili S; svaki X je nezavisno CH ili N; R1 je 5 do 7-člani zasićen ili nezasićen, po potrebi zamijenjen heterocikl koji sadrži najmanje 1 heteroatom izabran između N ili O; R2 je LY; svaki L je direktna veza, C1-C10 alkilen, C2-C10 alkenilen ili C2-C10 alkinilen; Y je po potrebi zamijenjen spojeni, premošćeni ili spirociklični nearomatični 5-12-člani heterocikl koji sadrži do 4 heteroatoma izabranih između N ili O; i svaki R3 je nezavisno H, C1-C10 alkil, halogen, fluoro C1-C10 alkil, O-C1-C10 alkil, NH-C1-C10 alkil, S-C1-C10 alkil, O-fluoro C1-C10 alkil, NH-acil, NH-C(O)-NH-C1-C10 alkil, C(O)-NH-C1-C10 alkil, aril ili heteroaril.
2. Sastav prema zahtjevu 1, gdje je spoj prema formuli I prisutno u količini od 0.1 do 50 masenih % na osnovu ukupne mase sastava, poželjno 5 do 30 masenih % na osnovu ukupne mase sastava.
3. Kompozicija prema zahtjevima 1 ili 2, gdje je punilo sredstvo za punjenje prisutno u količini od 10 do 90 masenih % na osnovu ukupne mase sastava, i/ili gdje je vezivno sredstvo prisutno u količini od 0.1 do 20 masenih % na osnovu ukupne mase sastava, i/ili gdje je dezintegrant prisutan u količini sa od 1 do 20 masenih % na osnovu ukupne mase sastava, i/ili gdje je lubrikans prisutan u količini sa od 0.1 do 10 masenih %, poželjno od 0.5 do 5 masenih % na osnovu ukupne mase kompozicije.
4. Sastav prema bilo kojem od prethodnih zahtjeva, gdje sastav obuhvaća: 1 do 50 masenih % spojeva prema zahtjevu 1; 10 do 90 masenih % najmanje jednog punila ; 0.1 do 20 masenih % najmanje jednog vezivnog sredstva; 1 do 20 masenih % najmanje jednog dezintegranta; i 0.1 do 10 masenih % od najmanje jednog lubrikanta ili sredstva za klizanje.
5. Farmaceutski sastav koja sadrži spoj formule I ili njegovu farmaceutski prihvatljivu sol, i najmanje jedno farmaceutsko pomoćno sredstvo izabrano iz grupe koju čine punila, vezivna sredstva, dezintegranti, sredstva za klizanje i lubrikanti, pri čemu je spoj prema formuli I predstavljen: [image] pri čemu: W je O, N-H, N-(C1-C10 alkil) ili S; svaki X je nezavisno CH ili N; R1 je 5 do 7-člani zasićen ili nezasićen, po potrebi zamijenjen heterocikl koji sadrži najmanje 1 heteroatom izabran između N ili O; R2 je LY; svaki L je direktna veza, C1-C10 alkilen, C2-C10 alkenilen ili C2-C10 alkinilen; Y je po potrebi zamijenjen spojeni, premošćeni ili spirociklični nearomatični 5-12-člani heterocikl koji sadrži do 4 heteroatoma izabranih između N ili O; i svaki R3 je nezavisno H, C1-C10 alkil, halogen, fluoro C1-C10 alkil, O-C1-C10 alkil, NH-C1-C10 alkil, S-C1-C10 alkil, O-fluoro C1-C10 alkil, NH-acil, NH-C(O)-NH-C1-C10 alkil, C(O)-NH-C1-C10 alkil, aril ili heteroaril; sastav obuhvaća: 1 do 50 masenih % spojeva formule I ili njegove farmaceutski prihvatljive soli; 10 do 90 masenih % najmanje jednog punila; 0.1 do 20 masenih % najmanje jednog vezivnog sredstva; 1 do 20 masenih % najmanje jednog dezintegranta; i 0.1 do 10 masenih % najmanje jednog lubrikanta ili sredstva za klizanje.
6. Sastav prema zahtjevu 5, što je spoj prema formuli I u obliku svoje sukcinatne soli.
7. Sastav prema bilo kojem od prethodnih zahtjeva, koje dalje sadrži površinski aktivnu supstancu, poželjno u količini od 0.1 do 5 masenih % na osnovu ukupne mase sastava.
8. Sastav prema bilo kojem od prethodnih zahtjeva, gdje je kompozicija u obliku čvrstog doznog oblika, poželjno oralnog čvrstog doznog oblika, poželjno u obliku tablete ili kapsule.
9. Sastav prema bilo kojem od prethodnih zahtjeva, gdje kompozicija obuhvaća najmanje dva ili najmanje tri farmaceutska pomoćna sredstva.
10. Sastav prema bilo kojem od zahtjeva 5 do 9, gdje je lubrikant prisutan u količini od 0.5 do 5 masenih % na osnovu ukupne mase sastava.
11. Sastav prema bilo kojem od prethodnih zahtjeva, gdje je R1 predstavljen bilo kojom od sljedećih struktura : [image] poželjno gdje je R1 morfolin.
12. Sastav prema bilo kojem od prethodnih zahtjeva, pri čemu W je O ili S, poželjno gdje W je O i/ili gde X je CH, i/ili gde R3 jeH, i/ili gde L je C1-C10 alkilen, poželjno metilen.
13. Sastav prema bilo kojem od prethodnih zahtjeva, gdje Y sadrži jedan ili dva heteroatoma, poželjno dva heteroatoma.
14. Sastav prema bilo kojem od prethodnih zahtjeva, pri čemu je Y izabran između: [image] pri čemu: A je izabrano između O, S, NR4 ili po potrebi zamijenjen C1-C3 alkilen, C2-C3 alkenilen, ili C2-C3 alkinilen; B je NR4, O ili CH2; pri čemu R4 je H ili po potrebi zamijenjen C1-C10 alkil, C2-C10 alkenil ili C2-C10 alkinil; p može biti 0 ili 1; svako m je nezavisno izabrano između 0, 1 ili 2; i svako n je nezavisno izabrano između 1, 2 ili 3.
15. Sastav prema bilo kojem od prethodnih zahtjeva, gdje je spoj prema formuli I prikazano bilo kojom od sljedećih struktura: [image] [image] [image] [image]
16. Sastav prema bilo kojem od prethodnih zahtjeva, za upotrebu u terapiji.
17. Sastav za upotrebu prema zahtjevu 16, gdje je terapija rak, poželjno leukemija ili PTEN- negativan solidan tumor, imunološki poremećaj ili inflamatorni poremećaj, poželjno reumatoidni artritis.
18. Postupak za proizvodnju farmaceutskog sastava, prema bilo kojem od zahtjeva 1 do 15, koji obuhvaća: a) miješanje spojeva prema formuli I sa najmanje jednim farmaceutskim pomoćnim sredstvom izabranim iz grupe koju čine punila, vezivna sredstva, dezintegranti, sredstva za klizanje i lubrikanti da bi se formirala smijesa; b) prerada smijese u farmaceutski sastav; ili c) komprimiranje sastava iz koraka (b) u tabletu, po potrebi, pri čemu korak (b) dalje obuhvaća prosijavanje kako bi se osigurala veličina čestica manja od 1000 μm, poželjno manja od 500 μm.
HRP20230362TT 2015-08-19 2016-08-19 Kompozicije koje sadrže triciklične heterorociklične spojeve HRP20230362T1 (hr)

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GBGB1514758.0A GB201514758D0 (en) 2015-08-19 2015-08-19 Formulation
EP16756765.0A EP3337460B1 (en) 2015-08-19 2016-08-19 Compositions comprising tricyclic heterocyclic compounds
PCT/GB2016/052577 WO2017029518A1 (en) 2015-08-19 2016-08-19 Compositions comprising tricyclic heterocyclic compounds

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US (2) US20180235974A1 (hr)
EP (1) EP3337460B1 (hr)
JP (1) JP6986757B2 (hr)
KR (1) KR20180066041A (hr)
CN (1) CN108135855B (hr)
AU (1) AU2016307886B9 (hr)
CA (1) CA2995896A1 (hr)
DK (1) DK3337460T3 (hr)
ES (1) ES2941741T3 (hr)
GB (1) GB201514758D0 (hr)
HK (1) HK1251465A1 (hr)
HR (1) HRP20230362T1 (hr)
IL (1) IL257501B (hr)
LT (1) LT3337460T (hr)
MX (1) MX2018001925A (hr)
PT (1) PT3337460T (hr)
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Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2534326T3 (es) 2009-08-20 2015-04-21 Karus Therapeutics Limited Compuestos tricíclicos heterocíclicos como inhibidores de la fosfoinositida 3-cinasa
GB201204125D0 (en) 2012-03-08 2012-04-25 Karus Therapeutics Ltd Compounds
GB201402431D0 (en) 2014-02-12 2014-03-26 Karus Therapeutics Ltd Compounds
GB201514758D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Formulation
GB201514754D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds
GB201514760D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds and method of use
GB201514751D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds

Family Cites Families (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1445742A1 (de) 1963-11-06 1968-12-19 Bayer Ag Verfahren zur Herstellung von 2-Stellung substituierten Benzoxazinonen
US4017500A (en) 1973-07-16 1977-04-12 Schering Corporation Certain 8-amino-1,7-naphthyridines
BE786081A (fr) 1971-07-13 1973-01-10 Uniroyal Sa Appareil et procede pour maintenir les tringles des bourrelets de pneu
US5703075A (en) 1988-12-21 1997-12-30 Pharmacia & Upjohn Company Antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones
UA72922C2 (uk) * 1999-08-03 2005-05-16 Ліллі Айкос Ллк ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ З <font face="Symbol">b</font>-КАРБОЛІНОМ (ВАРІАНТИ) ТА СПОСІБ ЛІКУВАННЯ СЕКСУАЛЬНОЇ ДИСФУНКЦІЇ
US6608053B2 (en) 2000-04-27 2003-08-19 Yamanouchi Pharmaceutical Co., Ltd. Fused heteroaryl derivatives
DE60144322D1 (de) 2000-04-27 2011-05-12 Astellas Pharma Inc Kondensierte heteroarylderivate
AU2001270260A1 (en) 2000-06-30 2002-01-14 Sugen, Inc. 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors
US6905669B2 (en) 2001-04-24 2005-06-14 Supergen, Inc. Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase
CA2491191C (en) 2002-07-15 2014-02-04 Exelixis, Inc. Receptor-type kinase modulators and methods of use
FR2846657B1 (fr) 2002-11-05 2004-12-24 Servier Lab Nouveaux composes pyridopyrimidinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
CA2557541C (en) 2004-02-26 2014-12-16 Aska Pharmaceutical Co., Ltd. Pyrimidine derivatives
EP1755609A1 (en) 2004-05-25 2007-02-28 Icos Corporation Methods for treating and/or preventing aberrant proliferation of hematopoietic cells
GB0423653D0 (en) 2004-10-25 2004-11-24 Piramed Ltd Pharmaceutical compounds
MX2007014619A (es) 2005-05-20 2009-02-13 Vertex Pharma Pirrolopiridinas de utilidad como inhibidores de proteina quinasa.
CA2635899A1 (en) 2006-01-19 2007-07-26 Osi Pharmaceuticals, Inc. Fused heterobicyclic kinase inhibitors
BRPI0710866A2 (pt) 2006-04-26 2012-08-14 Hoffmann La Roche compostos farmacÊuticos
EP2046799B1 (en) 2006-04-26 2017-07-19 Genentech, Inc. Phosphoinositide 3-kinase inhibitor compounds and pharmaceutical compositions containing them
ATE510840T1 (de) 2006-06-26 2011-06-15 Ucb Pharma Sa Kondensierte thiazol-derivate als kinasehemmer
CA2669399A1 (en) 2006-11-13 2008-05-29 Eli Lilly & Co. Thienopyrimidinones for treatment of inflammatory disorders and cancers
WO2008076447A2 (en) 2006-12-15 2008-06-26 Ordway Research Institute Treatments of therapy-resistant diseases comprising drug combinations
WO2008094992A2 (en) 2007-01-31 2008-08-07 Vertex Pharmaceuticals Incorporated 2-aminopyridine derivatives useful as kinase inhibitors
US20100063032A1 (en) 2007-03-28 2010-03-11 Debenham John S Substituted pyrido[2,3-d]pyrimidine derivatives as cannabinoid-1 receptor modulators
WO2008150827A1 (en) 2007-05-29 2008-12-11 Smithkline Beecham Corporation Naphthyridine, derivatives as p13 kinase inhibitors
GB0710528D0 (en) 2007-06-01 2007-07-11 Glaxo Group Ltd Novel compounds
US20110201608A1 (en) 2008-08-05 2011-08-18 Boehringer Ingelheim International Gmbh Substituted naphthyridines and use thereof as medicines
EP2344490A2 (en) 2008-10-03 2011-07-20 Merck Serono S.A. 4-morpholino-pyrido[3,2-d]pyrimidines active on pi3k
GB2465405A (en) 2008-11-10 2010-05-19 Univ Basel Triazine, pyrimidine and pyridine analogues and their use in therapy
WO2011012883A1 (en) 2009-07-29 2011-02-03 Karus Therapeutics Limited Benzo [e] [1, 3 ] oxazin-4-one derivatives as phosphoinositide 3-kinase inhibitors
ES2534326T3 (es) * 2009-08-20 2015-04-21 Karus Therapeutics Limited Compuestos tricíclicos heterocíclicos como inhibidores de la fosfoinositida 3-cinasa
US20110207736A1 (en) 2009-12-23 2011-08-25 Gatekeeper Pharmaceuticals, Inc. Compounds that modulate egfr activity and methods for treating or preventing conditions therewith
GB201007347D0 (en) 2010-04-30 2010-06-16 Karus Therapeutics Ltd Compounds
EP2518070A1 (en) * 2011-04-29 2012-10-31 Almirall, S.A. Pyrrolotriazinone derivatives as PI3K inhibitors
MY161925A (en) 2011-07-27 2017-05-15 Astrazeneca Ab 2 - (2, 4, 5 - substituted -anilino) pyrimidine derivatives as egfr modulators useful for treating cancer
WO2013017480A1 (en) 2011-07-29 2013-02-07 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
GB201204125D0 (en) 2012-03-08 2012-04-25 Karus Therapeutics Ltd Compounds
EP2922851B8 (en) 2012-11-20 2017-09-27 F. Hoffmann-La Roche AG Aminopyrimidine compounds as inhibitors of t790m containing egfr mutants
SI2994465T1 (sl) 2013-05-10 2018-10-30 Karus Therapeutics Limited Novi inhibitorji histon deacetilaze
AU2014273946B2 (en) 2013-05-30 2020-03-12 Infinity Pharmaceuticals, Inc. Treatment of cancers using PI3 kinase isoform modulators
WO2014210354A1 (en) 2013-06-28 2014-12-31 Genentech, Inc. Azaindazole compounds as inhibitors of t790m containing egfr mutants
JP6626437B2 (ja) 2013-10-08 2019-12-25 アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. ヒストンデアセチラーゼ阻害剤とHer2阻害剤またはPI3K阻害剤のいずれかの組み合わせ
US20150105383A1 (en) 2013-10-10 2015-04-16 Acetylon Pharmaceuticals, Inc. HDAC Inhibitors, Alone Or In Combination With PI3K Inhibitors, For Treating Non-Hodgkin's Lymphoma
GB201321730D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
GB201321728D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
GB201321738D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic Agents
GB201321729D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
GB201402431D0 (en) 2014-02-12 2014-03-26 Karus Therapeutics Ltd Compounds
MA40933A (fr) * 2014-11-11 2017-09-19 Piqur Therapeutics Ag Difluorométhyl-aminopyridines et difluorométhyl-aminopyrimidines
GB201514758D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Formulation
GB201514754D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds
GB201514760D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds and method of use
GB201514751D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds
GB201514756D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compound and method of use
GB201909468D0 (en) 2019-07-01 2019-08-14 Karus Therapeutics Ltd Compounds for treating cancer

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WO2017029518A1 (en) 2017-02-23
MX2018001925A (es) 2018-06-19
IL257501A (en) 2018-04-30
LT3337460T (lt) 2023-03-27
AU2016307886A1 (en) 2018-03-08
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SI3337460T1 (sl) 2023-04-28
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