|
EP1912636B1
(en)
*
|
2005-07-21 |
2014-06-25 |
Ardea Biosciences, Inc. |
N-(arylamino)-sulfonamide inhibitors of mek
|
|
US8101799B2
(en)
|
2005-07-21 |
2012-01-24 |
Ardea Biosciences |
Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK
|
|
US7919598B2
(en)
*
|
2006-06-28 |
2011-04-05 |
Bristol-Myers Squibb Company |
Crystal structures of SGLT2 inhibitors and processes for preparing same
|
|
JO2985B1
(ar)
|
2006-12-20 |
2016-09-05 |
Takeda Pharmaceuticals Co |
مثبطات كينازmapk/erk
|
|
ES2320955B1
(es)
|
2007-03-02 |
2010-03-16 |
Laboratorios Almirall S.A. |
Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida.
|
|
JP5363350B2
(ja)
|
2007-03-19 |
2013-12-11 |
武田薬品工業株式会社 |
Mapk/erkキナーゼ阻害剤
|
|
ES2329639B1
(es)
|
2007-04-26 |
2010-09-23 |
Laboratorios Almirall S.A. |
Nuevos derivados de 4,8-difenilpoliazanaftaleno.
|
|
US8569378B2
(en)
|
2007-07-20 |
2013-10-29 |
Toshiyuki Sakai |
p27 protein inducer
|
|
US8022057B2
(en)
|
2007-11-12 |
2011-09-20 |
Takeda Pharmaceutical Company Limited |
MAPK/ERK kinase inhibitors
|
|
US20090246198A1
(en)
*
|
2008-03-31 |
2009-10-01 |
Takeda Pharmaceutical Company Limited |
Mapk/erk kinase inhibitors and methods of use thereof
|
|
EP2108641A1
(en)
|
2008-04-11 |
2009-10-14 |
Laboratorios Almirall, S.A. |
New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
|
|
EP2113503A1
(en)
|
2008-04-28 |
2009-11-04 |
Laboratorios Almirall, S.A. |
New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors
|
|
UA103319C2
(en)
|
2008-05-06 |
2013-10-10 |
Глаксосмитклайн Ллк |
Thiazole- and oxazole-benzene sulfonamide compounds
|
|
RU2399621C2
(ru)
*
|
2008-10-14 |
2010-09-20 |
Андрей Александрович Иващенко |
ЗАМЕЩЕННЫЕ 2-АЛКИЛАМИНО-3-СУЛЬФОНИЛ-ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ, АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-HT6 РЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
|
|
RU2393157C1
(ru)
*
|
2008-10-06 |
2010-06-27 |
Андрей Александрович Иващенко |
2-АЛКИЛАМИНО-3-АРИЛСУЛЬФОНИЛ-ПИРАЗОЛО[1,5-а]ПИРИМИДИНЫ, АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-HT6 РЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
|
|
EP2346818B1
(en)
|
2008-11-10 |
2012-12-05 |
Bayer Intellectual Property GmbH |
Substituted sulphonamido phenoxybenzamides
|
|
JP5743897B2
(ja)
|
2008-11-20 |
2015-07-01 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC |
化合物
|
|
US9084781B2
(en)
|
2008-12-10 |
2015-07-21 |
Novartis Ag |
MEK mutations conferring resistance to MEK inhibitors
|
|
CA2755561A1
(en)
*
|
2009-03-26 |
2010-09-30 |
Mapi Pharma Limited |
Process for the preparation of alogliptin
|
|
CN101619063B
(zh)
*
|
2009-06-02 |
2011-08-10 |
华中师范大学 |
具有抗肿瘤活性的3,7,8-多取代吡啶并[4,3-d]嘧啶衍生物及制备
|
|
WO2011031308A1
(en)
*
|
2009-09-09 |
2011-03-17 |
Cytokinetics, Incorporated |
Novel combinations
|
|
AU2010298277B2
(en)
*
|
2009-09-23 |
2014-07-03 |
Novartis Ag |
Combination
|
|
CA2775125C
(en)
*
|
2009-09-23 |
2019-01-08 |
Glaxosmithkline Llc |
Combination of a mek inhibitor and an akt inhibitor to treat cancer
|
|
EA201270475A1
(ru)
|
2009-09-28 |
2012-11-30 |
ГЛЭКСОСМИТКЛАЙН ЭлЭлСи |
Комбинация
|
|
KR20120100978A
(ko)
*
|
2009-10-08 |
2012-09-12 |
글락소스미스클라인 엘엘씨 |
조합물
|
|
ES2745479T3
(es)
*
|
2009-10-16 |
2020-03-02 |
Novartis Ag |
Combinación que comprende un inhibidor de MEK y un inhibidor de B-raf
|
|
WO2011047788A1
(en)
|
2009-10-21 |
2011-04-28 |
Bayer Schering Pharma Aktiengesellschaft |
Substituted benzosulphonamides
|
|
EP2491014A1
(en)
|
2009-10-21 |
2012-08-29 |
Bayer Pharma Aktiengesellschaft |
Substituted halophenoxybenzamide derivatives
|
|
CA2777430A1
(en)
|
2009-10-21 |
2011-04-28 |
Bayer Pharma Aktiengesellschaft |
Substituted benzosulphonamides
|
|
EA022637B1
(ru)
*
|
2009-11-17 |
2016-02-29 |
ГЛЭКСОСМИТКЛАЙН ЭлЭлСи |
Комбинация
|
|
RU2421456C1
(ru)
*
|
2010-02-26 |
2011-06-20 |
Общество С Ограниченной Ответственностью "Инновационная Фармацевтика" |
ЗАМЕЩЕННЫЕ 3-АРИЛСУЛЬФОНИЛ-ПИРАЗОЛО[1,5-a]ПИРИМИДИН-2,6-ДИАМИНЫ, АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-НТ6 РЕЦЕПТОРОВ, СПОСОБЫ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
|
|
UY33288A
(es)
*
|
2010-03-25 |
2011-10-31 |
Glaxosmithkline Llc |
Derivados de indolina inhibidores de la proteina quinasa r del reticulo endoplasmatico
|
|
BR112012024380A2
(pt)
|
2010-03-25 |
2015-09-15 |
Glaxosmithkline Llc |
compostos químicos
|
|
ES2689177T3
(es)
*
|
2010-04-13 |
2018-11-08 |
Novartis Ag |
Combinación que comprende un inhibidor de cinasa 4 dependiente de ciclina o cinasa dependiente de ciclina (CDK4/6) y un inhibidor de mTOR para tratar cáncer
|
|
WO2011146712A1
(en)
|
2010-05-21 |
2011-11-24 |
Glaxosmithkline Llc |
Combination
|
|
UA112517C2
(uk)
|
2010-07-06 |
2016-09-26 |
Новартіс Аг |
Тетрагідропіридопіримідинові похідні
|
|
US20130165456A1
(en)
|
2010-08-26 |
2013-06-27 |
Tona M. Gilmer |
Combination
|
|
WO2012055953A1
(en)
|
2010-10-29 |
2012-05-03 |
Bayer Pharma Aktiengesellschaft |
Substituted phenoxypyridines
|
|
CN102020651B
(zh)
|
2010-11-02 |
2012-07-18 |
北京赛林泰医药技术有限公司 |
6-芳基氨基吡啶酮甲酰胺mek抑制剂
|
|
WO2012061683A2
(en)
*
|
2010-11-05 |
2012-05-10 |
Glaxosmithkline Llc |
Methods for treating cancer
|
|
US20130231346A1
(en)
*
|
2010-11-17 |
2013-09-05 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Methods of treating cancer
|
|
CA2818544A1
(en)
*
|
2010-11-19 |
2012-05-24 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Method of treatment with braf inhibitor
|
|
JP6063871B2
(ja)
*
|
2010-12-20 |
2017-01-18 |
ノバルティス アーゲー |
組合せ
|
|
TWI505828B
(zh)
|
2010-12-20 |
2015-11-01 |
葛蘭素史克智慧財產(第二)有限公司 |
新穎醫藥組成物
|
|
WO2012088266A2
(en)
|
2010-12-22 |
2012-06-28 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3
|
|
WO2013019620A2
(en)
*
|
2011-07-29 |
2013-02-07 |
Glaxosmithkline Llc |
Method of treating cancer using combination of braf inhibitor, mek inhibitor, and anti-ctla-4 antibody
|
|
AR087405A1
(es)
*
|
2011-08-01 |
2014-03-19 |
Genentech Inc |
Metodos para tratar el cancer por el uso de antagonistas de union al eje pd-1 e inhibidores de mek
|
|
US9675595B2
(en)
|
2011-08-31 |
2017-06-13 |
Novartis Ag |
Synergistic combinations of PI3K- and MEK-inhibitors
|
|
PL2790705T3
(pl)
|
2011-12-15 |
2018-06-29 |
Novartis Ag |
Zastosowanie inhibitorów czynności lub funkcji PI3K
|
|
UA114906C2
(uk)
*
|
2012-03-14 |
2017-08-28 |
Люпін Лімітед |
Гетероциклільні сполуки як інгібітори мек
|
|
US20150141470A1
(en)
|
2012-05-08 |
2015-05-21 |
The Broad Institute, Inc. |
Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy
|
|
HUE042374T2
(hu)
|
2012-06-13 |
2019-06-28 |
Incyte Holdings Corp |
Szubsztituált triciklusos vegyületek mint FGFR inhibitorok
|
|
US9388185B2
(en)
|
2012-08-10 |
2016-07-12 |
Incyte Holdings Corporation |
Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
|
|
LT2892535T
(lt)
*
|
2012-09-04 |
2021-12-10 |
Novartis Ag |
Adjuvantinis vėžio gydymo būdas
|
|
EP2911673A4
(en)
*
|
2012-10-25 |
2016-05-18 |
Novartis Ag |
COMBINATION
|
|
EP2925366B1
(en)
|
2012-11-29 |
2018-02-21 |
Novartis AG |
Pharmaceutical combinations
|
|
MX2015006867A
(es)
*
|
2012-11-30 |
2015-10-05 |
Glaxosmithkline Llc |
Composicion farmaceutica novedosa.
|
|
US9266892B2
(en)
|
2012-12-19 |
2016-02-23 |
Incyte Holdings Corporation |
Fused pyrazoles as FGFR inhibitors
|
|
EP2752191A1
(en)
|
2013-01-07 |
2014-07-09 |
Sanofi |
Compositions and methods using hdm2 antagonist and mek inhibitor
|
|
US20150342957A1
(en)
|
2013-01-09 |
2015-12-03 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Combination
|
|
US10139415B2
(en)
|
2013-02-27 |
2018-11-27 |
Daiichi Sankyo Company, Limited |
Method for predicting responsiveness to compound inhibiting MAPK signal transduction pathway
|
|
KR102469849B1
(ko)
|
2013-04-19 |
2022-11-23 |
인사이트 홀딩스 코포레이션 |
Fgfr 저해제로서 이환식 헤테로사이클
|
|
AR096433A1
(es)
|
2013-05-28 |
2015-12-30 |
Glaxosmithkline Intellectual Property (No 2) Ltd |
Método de tratamiento del cáncer y uso
|
|
BR112015028326A8
(pt)
|
2013-06-03 |
2018-01-23 |
Novartis Ag |
combinações de anticorpo anti-pd-l1, inibidor de mek e/ou inibidor de braf, seus kits e seus usos, e composição farmacêutica
|
|
WO2015056180A1
(en)
|
2013-10-15 |
2015-04-23 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Indoline derivatives as inhibitors of perk
|
|
KR102222569B1
(ko)
|
2013-10-25 |
2021-03-05 |
샹하이 헨그루이 파마수티컬 컴퍼니 리미티드 |
피리딘의 케톤 유도체의 제조 방법 및 제약 용도
|
|
WO2015059677A1
(en)
|
2013-10-26 |
2015-04-30 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Methods of treating cancer
|
|
CN104918937B
(zh)
*
|
2013-12-06 |
2016-09-14 |
杭州普晒医药科技有限公司 |
曲美替尼及其溶剂化物的晶型、其制备方法、含有它们的药物组合物及其用途
|
|
WO2015087279A1
(en)
|
2013-12-12 |
2015-06-18 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Combinations of trametinib, panitumumab and dabrafenib for the treatment of cancer
|
|
JOP20200094A1
(ar)
|
2014-01-24 |
2017-06-16 |
Dana Farber Cancer Inst Inc |
جزيئات جسم مضاد لـ pd-1 واستخداماتها
|
|
JOP20200096A1
(ar)
|
2014-01-31 |
2017-06-16 |
Children’S Medical Center Corp |
جزيئات جسم مضاد لـ tim-3 واستخداماتها
|
|
EP2913048A1
(en)
*
|
2014-02-27 |
2015-09-02 |
ratiopharm GmbH |
Pharmaceutical composition comprising trametinib
|
|
KR20240110004A
(ko)
|
2014-03-14 |
2024-07-12 |
노파르티스 아게 |
Lag-3에 대한 항체 분자 및 그의 용도
|
|
SG10202007111TA
(en)
|
2014-07-15 |
2020-09-29 |
Genentech Inc |
Compositions for treating cancer using pd-1 axis binding antagonists and mek inhibitors
|
|
WO2016009306A1
(en)
|
2014-07-15 |
2016-01-21 |
Lupin Limited |
Heterocyclyl compounds as mek inhibitors
|
|
WO2016035008A1
(en)
|
2014-09-04 |
2016-03-10 |
Lupin Limited |
Pyridopyrimidine derivatives as mek inhibitors
|
|
ES2771926T3
(es)
|
2014-09-13 |
2020-07-07 |
Novartis Ag |
Terapias de combinación
|
|
JP2017535528A
(ja)
|
2014-10-03 |
2017-11-30 |
ノバルティス アーゲー |
組み合わせ治療
|
|
WO2016055935A1
(en)
|
2014-10-06 |
2016-04-14 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Combination of lysine-specific demethylase 1 inhibitor and thrombopoietin agonist
|
|
US9988452B2
(en)
|
2014-10-14 |
2018-06-05 |
Novartis Ag |
Antibody molecules to PD-L1 and uses thereof
|
|
WO2016059602A2
(en)
|
2014-10-16 |
2016-04-21 |
Glaxo Group Limited |
Methods of treating cancer and related compositions
|
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
|
EP3233918A1
(en)
|
2014-12-19 |
2017-10-25 |
Novartis AG |
Combination therapies
|
|
AU2016219822B2
(en)
|
2015-02-20 |
2020-07-09 |
Incyte Holdings Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
|
MA41551A
(fr)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
|
|
WO2016134294A1
(en)
|
2015-02-20 |
2016-08-25 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
|
JP2016155776A
(ja)
*
|
2015-02-24 |
2016-09-01 |
学校法人兵庫医科大学 |
抗腫瘍効果増強剤および抗腫瘍剤
|
|
CZ2015278A3
(cs)
|
2015-04-24 |
2016-11-02 |
Zentiva, K.S. |
Krystalické formy trametinibu
|
|
CN108025051B
(zh)
|
2015-07-29 |
2021-12-24 |
诺华股份有限公司 |
包含抗pd-1抗体分子的联合疗法
|
|
WO2017019894A1
(en)
|
2015-07-29 |
2017-02-02 |
Novartis Ag |
Combination therapies comprising antibody molecules to lag-3
|
|
EP3878465A1
(en)
|
2015-07-29 |
2021-09-15 |
Novartis AG |
Combination therapies comprising antibody molecules to tim-3
|
|
CN111821306A
(zh)
|
2015-08-28 |
2020-10-27 |
诺华股份有限公司 |
Mdm2抑制剂和其组合
|
|
WO2017037574A1
(en)
|
2015-08-28 |
2017-03-09 |
Novartis Ag |
Combinations of the cdk4/6 inhibitor lee011 and the mek1/2 inhibitor trametinib, optionally further comprising the pi3k inhibitor byl719 to treat cancer
|
|
HRP20220436T1
(hr)
|
2015-11-03 |
2022-05-27 |
Janssen Biotech, Inc. |
Protutijela koja se specifično vežu na pd-1 i njihove uporabe
|
|
RU2605400C1
(ru)
*
|
2015-11-13 |
2016-12-20 |
ЗАО "Р-Фарм" |
ПРОИЗВОДНЫЕ 1-(3-АМИНОФЕНИЛ)-6,8-ДИМЕТИЛ-5-(4-ИОД-2-ФТОР-ФЕНИЛАМИНО)-3-ЦИКЛОПРОПИЛ-1H,6H-ПИРИДО[4,3-d]ПИРИМИДИН-2,4,7-ТРИОНА В КАЧЕСТВЕ ИНГИБИТОРОВ МЕК1/2
|
|
WO2017098421A1
(en)
|
2015-12-08 |
2017-06-15 |
Glaxosmithkline Intellectual Property Development Limited |
Benzothiadiazine compounds
|
|
CA3007671A1
(en)
|
2015-12-17 |
2017-06-22 |
Novartis Ag |
Antibody molecules to pd-1 and uses thereof
|
|
US11883404B2
(en)
|
2016-03-04 |
2024-01-30 |
Taiho Pharmaceuticals Co., Ltd. |
Preparation and composition for treatment of malignant tumors
|
|
AU2017226389B2
(en)
|
2016-03-04 |
2023-02-02 |
Taiho Pharmaceutical Co., Ltd. |
Preparation and composition for treatment of malignant tumors
|
|
WO2017153952A1
(en)
|
2016-03-10 |
2017-09-14 |
Glaxosmithkline Intellectual Property Development Limited |
5-sulfamoyl-2-hydroxybenzamide derivatives
|
|
KR102341660B1
(ko)
|
2016-09-19 |
2021-12-23 |
노파르티스 아게 |
Raf 억제제 및 erk 억제제를 포함하는 치료적 조합
|
|
RU2627692C1
(ru)
*
|
2016-10-10 |
2017-08-10 |
Закрытое акционерное общество "Р-Фарм" (ЗАО "Р-Фарм") |
N-{ 3-[3-циклопропил-5-(2-фторо-4-иодофениламино)-6,8-диметил-2,4,7-триоксо-3,4,6,7-тетрагидро-2Н-пиридо[4,3-d]пиримидин-1-ил]-фенил} -циклопропанкарбоксамида диметилсульфоксида сольват в качестве ингибитора МЕК1/2
|
|
CN107970246B
(zh)
*
|
2016-10-21 |
2020-08-28 |
中山大学 |
非甾体类抗炎药在提高肿瘤细胞对酪氨酸激酶抑制剂的敏感性中的应用
|
|
WO2018092064A1
(en)
|
2016-11-18 |
2018-05-24 |
Novartis Ag |
Combinations of mdm2 inhibitors and bcl-xl inhibitors
|
|
CN109073634B
(zh)
|
2016-11-25 |
2022-07-08 |
基诺富公司 |
用于诱导神经干细胞的分化和保护的组合物及使用该组合物诱导神经再生的方法
|
|
CN110225983A
(zh)
|
2016-12-01 |
2019-09-10 |
葛兰素史密斯克莱知识产权发展有限公司 |
治疗癌症的方法
|
|
ES2952265T3
(es)
|
2017-05-02 |
2023-10-30 |
Novartis Ag |
Terapia combinada que comprende un inhibidor de Raf y trametinib
|
|
AR111960A1
(es)
|
2017-05-26 |
2019-09-04 |
Incyte Corp |
Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
|
|
UY37866A
(es)
|
2017-09-07 |
2019-03-29 |
Glaxosmithkline Ip Dev Ltd |
Nuevos compuestos derivados de benzoimidazol sustituidos que reducen la proteína myc (c-myc) en las células e inhiben la histona acetiltransferasa de p300/cbp.
|
|
WO2019053617A1
(en)
|
2017-09-12 |
2019-03-21 |
Glaxosmithkline Intellectual Property Development Limited |
CHEMICAL COMPOUNDS
|
|
MX2020004756A
(es)
|
2017-11-16 |
2020-08-20 |
Novartis Ag |
Terapias de combinacion.
|
|
US12398209B2
(en)
|
2018-01-22 |
2025-08-26 |
Janssen Biotech, Inc. |
Methods of treating cancers with antagonistic anti-PD-1 antibodies
|
|
PL3769765T3
(pl)
|
2018-03-19 |
2024-06-10 |
Taiho Pharmaceutical Co., Ltd. |
Kompozycja farmaceutyczna zawierająca alkilosiarczan sodu
|
|
WO2019180141A1
(en)
|
2018-03-23 |
2019-09-26 |
Bayer Aktiengesellschaft |
Combinations of rogaratinib
|
|
KR20200138303A
(ko)
|
2018-03-30 |
2020-12-09 |
노파르티스 아게 |
다브라페닙, 트라메티닙 및 erk 저해제를 포함하는 삼중 약제학적 조합물
|
|
EP3560516A1
(en)
|
2018-04-27 |
2019-10-30 |
Bergen Teknologioverforing AS |
Combination therapy including beta-sitosterol in combination with at least one of a braf inhibitor, a mek inhibitor or an erk inhibitor and methods and use thereof
|
|
EP4309737A3
(en)
|
2018-05-04 |
2024-03-27 |
Incyte Corporation |
Solid forms of an fgfr inhibitor and processes for preparing the same
|
|
EP3788046B1
(en)
|
2018-05-04 |
2025-12-10 |
Incyte Corporation |
Salts of an fgfr inhibitor
|
|
SG11202011633SA
(en)
|
2018-05-24 |
2020-12-30 |
Janssen Biotech Inc |
Psma binding agents and uses thereof
|
|
AR116109A1
(es)
|
2018-07-10 |
2021-03-31 |
Novartis Ag |
Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos
|
|
EP3867409A1
(en)
|
2018-10-16 |
2021-08-25 |
Novartis AG |
Tumor mutation burden alone or in combination with immune markers as biomarkers for predicting response to targeted therapy
|
|
CN109320513B
(zh)
*
|
2018-11-09 |
2021-03-16 |
安庆奇创药业有限公司 |
一种合成曲美替尼的方法
|
|
MA55141A
(fr)
|
2018-11-20 |
2021-09-29 |
Nflection Therapeutics Inc |
Composés cyanoaryl-aniline pour le traitement d'affections de la peau
|
|
JP7393808B2
(ja)
*
|
2018-11-20 |
2023-12-07 |
エヌフレクション セラピューティクス インコーポレイテッド |
皮膚障害の処置のためのナフチリジノン-アニリン化合物
|
|
CN117551073A
(zh)
|
2018-11-20 |
2024-02-13 |
恩福莱克逊治疗有限公司 |
用于治疗皮肤疾病噻吩基苯胺化合物
|
|
AU2019390729B2
(en)
|
2018-11-30 |
2022-08-11 |
Glaxosmithkline Intellectual Property Development Limited |
Compounds useful in HIV therapy
|
|
AU2019402189B2
(en)
|
2018-12-20 |
2023-04-13 |
Novartis Ag |
Dosing regimen and pharmaceutical combination comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives
|
|
EP3920932A4
(en)
*
|
2019-02-06 |
2022-10-19 |
Aurobindo Pharma Limited |
METHOD FOR PREPARING AN ACETIC ACID SOLVATE OF TRAMETINIB
|
|
CN113329792B
(zh)
|
2019-02-15 |
2024-06-28 |
诺华股份有限公司 |
取代的3-(1-氧代异吲哚啉-2-基)哌啶-2,6-二酮衍生物及其用途
|
|
BR112021015783A2
(pt)
|
2019-02-15 |
2021-10-05 |
Novartis Ag |
Derivados de 3-(1-oxo-5-(piperidin-4-il)isoindolin-2-il)piperidina-2,6-diona e usos dos mesmos
|
|
US11628162B2
(en)
|
2019-03-08 |
2023-04-18 |
Incyte Corporation |
Methods of treating cancer with an FGFR inhibitor
|
|
BR112021020532A2
(pt)
|
2019-04-19 |
2022-03-15 |
Janssen Biotech Inc |
Métodos para tratamento de câncer de próstata com um anticorpo anti-psma/cd3
|
|
EP3969449B1
(en)
|
2019-05-13 |
2025-02-12 |
Novartis AG |
New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl)isonicotinamide as raf inhibitors for the treatment of cancer
|
|
US11591329B2
(en)
|
2019-07-09 |
2023-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
|
TW202114994A
(zh)
*
|
2019-07-29 |
2021-04-16 |
大陸商江蘇恆瑞醫藥股份有限公司 |
一種1,6-二氫吡啶-3-甲醯胺衍生物的製備方法
|
|
WO2021018941A1
(en)
|
2019-07-31 |
2021-02-04 |
Glaxosmithkline Intellectual Property Development Limited |
Methods of treating cancer
|
|
US12122767B2
(en)
|
2019-10-01 |
2024-10-22 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
|
WO2021076602A1
(en)
|
2019-10-14 |
2021-04-22 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
|
WO2021076728A1
(en)
|
2019-10-16 |
2021-04-22 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
|
KR20220131900A
(ko)
|
2019-12-04 |
2022-09-29 |
인사이트 코포레이션 |
Fgfr 억제제의 유도체
|
|
JP7720840B2
(ja)
|
2019-12-04 |
2025-08-08 |
インサイト・コーポレイション |
Fgfr阻害剤としての三環式複素環
|
|
AU2020406350A1
(en)
|
2019-12-20 |
2022-08-11 |
Novartis Ag |
Uses of anti-TGF-beta antibodies and checkpoint inhibitors for the treatment of proliferative diseases
|
|
WO2021142345A1
(en)
*
|
2020-01-08 |
2021-07-15 |
Icahn School Of Medicine At Mount Sinai |
Small molecule modulators ksr-bound mek
|
|
US12012409B2
(en)
|
2020-01-15 |
2024-06-18 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
|
US20230226030A1
(en)
|
2020-02-18 |
2023-07-20 |
Novartis Ag |
Therapeutic combinations comprising a raf inhibitor for use in treating braf mutant nsclc
|
|
TW202200146A
(zh)
|
2020-04-10 |
2022-01-01 |
日商大鵬藥品工業股份有限公司 |
使用有3,5-二取代苯炔基化合物與mek抑制劑之癌症治療法
|
|
WO2021209563A1
(en)
|
2020-04-16 |
2021-10-21 |
Som Innovation Biotech, S.A. |
Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus
|
|
US20240000789A1
(en)
|
2020-05-12 |
2024-01-04 |
Novartis Ag |
Therapeutic combinations comprising a craf inhibitor
|
|
US20230212164A1
(en)
*
|
2020-06-02 |
2023-07-06 |
Boehringer Ingelheim International Gmbh |
Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
|
|
CA3182346A1
(en)
|
2020-06-23 |
2021-12-30 |
Novartis Ag |
Dosing regimen comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives
|
|
EP4203963A1
(en)
|
2020-08-31 |
2023-07-05 |
Novartis AG |
Combination therapy of a raf inhibitor and a mek inhibitor for the treatment of sarcoma
|
|
CA3200814A1
(en)
|
2020-12-02 |
2022-06-09 |
Alfredo C. Castro |
Tead inhibitors and uses thereof
|
|
WO2022120353A1
(en)
|
2020-12-02 |
2022-06-09 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
|
EP4281073A1
(en)
|
2021-01-25 |
2023-11-29 |
Ikena Oncology, Inc. |
Combination of a 3-(imidazol-4-yl)-4-(amino)-benzenesulfonamide tead inhibitor with an egfr inhibitor and/or mek inhibitor for use in the treatment of lung cancer
|
|
CA3210246A1
(en)
|
2021-01-28 |
2022-08-04 |
Janssen Biotech, Inc. |
Psma binding proteins and uses thereof
|
|
IL304891A
(en)
|
2021-02-02 |
2023-10-01 |
Servier Lab |
Selective Protech BCL-XL compounds and methods of use
|
|
JP2024511373A
(ja)
|
2021-03-18 |
2024-03-13 |
ノバルティス アーゲー |
がんのためのバイオマーカーおよびその使用
|
|
TWI825637B
(zh)
|
2021-03-31 |
2023-12-11 |
美商輝瑞股份有限公司 |
啶-1,6(2h,7h)-二酮
|
|
TW202304979A
(zh)
|
2021-04-07 |
2023-02-01 |
瑞士商諾華公司 |
抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途
|
|
JP2024514127A
(ja)
|
2021-04-09 |
2024-03-28 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
抗がん剤療法
|
|
CA3215903A1
(en)
|
2021-04-12 |
2022-10-20 |
Incyte Corporation |
Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
|
|
JP2024514879A
(ja)
*
|
2021-04-16 |
2024-04-03 |
イケナ オンコロジー, インコーポレイテッド |
Mek阻害剤及びその使用
|
|
CN117177752A
(zh)
|
2021-05-05 |
2023-12-05 |
诺华股份有限公司 |
用于治疗mpnst的化合物和组合物
|
|
AR125874A1
(es)
|
2021-05-18 |
2023-08-23 |
Novartis Ag |
Terapias de combinación
|
|
WO2022261159A1
(en)
|
2021-06-09 |
2022-12-15 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
|
EP4352059A1
(en)
|
2021-06-09 |
2024-04-17 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
|
WO2022259157A1
(en)
|
2021-06-09 |
2022-12-15 |
Novartis Ag |
A triple pharmaceutical combination comprising dabrafenib, trametinib and a shp2 inhibitor
|
|
WO2023114984A1
(en)
|
2021-12-17 |
2023-06-22 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
|
TW202342766A
(zh)
|
2022-03-02 |
2023-11-01 |
瑞士商諾華公司 |
用於癌症治療之精準療法
|
|
CN114456166B
(zh)
*
|
2022-03-30 |
2023-06-16 |
沈阳药科大学 |
5-取代氨基-3-甲基吡啶并[2,3-d]嘧啶类化合物及其制备与应用
|
|
CN114605408B
(zh)
*
|
2022-03-30 |
2023-06-16 |
沈阳药科大学 |
5-羟基-1,3-二取代苯基吡啶并[2,3-d]嘧啶类化合物及其制法和应用
|
|
CN114573582B
(zh)
*
|
2022-03-30 |
2023-06-16 |
沈阳药科大学 |
1,2,3,4-四氢吡啶并[2,3-d]嘧啶类化合物及其制备方法和应用
|
|
CN114573581B
(zh)
*
|
2022-03-30 |
2023-09-01 |
沈阳药科大学 |
5-取代氨基-1,3-二取代苯基吡啶并[2,3-d]嘧啶类化合物及其制备与应用
|
|
IL317103A
(en)
|
2022-05-20 |
2025-01-01 |
Novartis Ag |
Antibody-drug conjugates of MET inhibitor BCL-XL and methods of using them
|
|
EP4525925A1
(en)
|
2022-05-20 |
2025-03-26 |
Novartis AG |
Epha2 bcl-xl inhibitor antibody-drug conjugates and methods of use thereof
|
|
CN114853754B
(zh)
*
|
2022-05-23 |
2023-04-18 |
云白药征武科技(上海)有限公司 |
一种硫代酰胺衍生物及其制备方法和应用
|
|
WO2023230205A1
(en)
|
2022-05-25 |
2023-11-30 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
|
AR129423A1
(es)
|
2022-05-27 |
2024-08-21 |
Viiv Healthcare Co |
Compuestos útiles en la terapia contra el hiv
|
|
AU2024234194A1
(en)
|
2023-03-10 |
2025-08-07 |
Novartis Ag |
Panras inhibitor antibody-drug conjugates and methods of use thereof
|
|
WO2025111450A1
(en)
|
2023-11-22 |
2025-05-30 |
Les Laboratoires Servier |
Anti-cd74 antibody-drug conjugates and methods of use thereof
|
|
WO2025132408A2
(en)
|
2023-12-21 |
2025-06-26 |
Synthon B.V. |
Solvates of trametinib
|
|
WO2025132190A1
(en)
|
2023-12-22 |
2025-06-26 |
Synthon B.V. |
A process for making trametinib
|
|
WO2025146444A1
(en)
|
2024-01-03 |
2025-07-10 |
Bayer Aktiengesellschaft |
Darolutamide in combination with braf and mek inhibitors for melanoma treatment
|
|
CN120441478A
(zh)
*
|
2024-02-07 |
2025-08-08 |
成都赜灵生物医药科技有限公司 |
一种六元内酰胺类化合物及其应用
|
|
WO2025215536A1
(en)
|
2024-04-10 |
2025-10-16 |
Novartis Ag |
Macrocyclic panras inhibitors for the treatment of cancer
|
|
CN118121604B
(zh)
*
|
2024-05-07 |
2024-06-25 |
四川成都中农大现代农业产业研究院 |
表没食子儿茶素没食子酸酯的组合物及其作为铜离子载体抗肝癌增敏剂的用途
|