EP1114053A1
(en)
|
1998-09-18 |
2001-07-11 |
Basf Aktiengesellschaft |
Pyrrolopyrimidines as protein kinase inhibitors
|
US6921763B2
(en)
|
1999-09-17 |
2005-07-26 |
Abbott Laboratories |
Pyrazolopyrimidines as therapeutic agents
|
DE60037455T2
(de)
|
1999-09-17 |
2008-11-27 |
Abbott Gmbh & Co. Kg |
Kinaseinhibitoren als arzneimittel
|
US6998391B2
(en)
|
2002-02-07 |
2006-02-14 |
Supergen.Inc. |
Method for treating diseases associated with abnormal kinase activity
|
US7405295B2
(en)
|
2003-06-04 |
2008-07-29 |
Cgi Pharmaceuticals, Inc. |
Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
|
US7393848B2
(en)
|
2003-06-30 |
2008-07-01 |
Cgi Pharmaceuticals, Inc. |
Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds
|
TWI372050B
(en)
|
2003-07-03 |
2012-09-11 |
Astex Therapeutics Ltd |
(morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles
|
CN1898240B
(zh)
|
2003-10-15 |
2011-08-03 |
Osi制药公司 |
咪唑并吡嗪类酪氨酸激酶抑制剂
|
CA2561950C
(en)
|
2004-04-02 |
2010-04-20 |
Osi Pharmaceuticals, Inc. |
6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors
|
EP1761540B1
(en)
|
2004-05-13 |
2016-09-28 |
Icos Corporation |
Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
|
WO2006055831A2
(en)
|
2004-11-17 |
2006-05-26 |
Miikana Therapeutics, Inc. |
Kinase inhibitors
|
NZ555158A
(en)
|
2004-11-18 |
2010-09-30 |
Synta Pharmaceuticals Corp |
Triazole compounds that modulate Hsp90 activity
|
CN101155800B
(zh)
|
2005-02-04 |
2012-05-23 |
阿斯利康(瑞典)有限公司 |
可用作激酶抑制剂的吡唑基氨基吡啶衍生物
|
CA2598383C
(en)
|
2005-02-18 |
2013-11-26 |
The Hong Kong Polytechnic University |
Method for asymmetric hydrosilylation of ketones
|
CA2622352C
(en)
|
2005-09-30 |
2014-05-27 |
Miikana Therapeutics, Inc. |
Substituted pyrazole compounds
|
CA2626375A1
(en)
|
2005-10-28 |
2007-05-03 |
Astrazeneca Ab |
4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer
|
US8153632B2
(en)
|
2005-11-16 |
2012-04-10 |
S*Bio Pte Ltd. |
Oxygen linked pyrimidine derivatives
|
ES2436877T3
(es)
|
2005-11-17 |
2014-01-07 |
OSI Pharmaceuticals, LLC |
Intermedios para la preparación de inhibidores de mTOR bicíclicos condensados
|
EP1954290B1
(en)
|
2005-11-22 |
2012-07-25 |
Merck Sharp & Dohme Corp. |
Tricyclic compounds useful as inhibitors of kinases
|
PE20070855A1
(es)
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
AR057960A1
(es)
|
2005-12-02 |
2007-12-26 |
Osi Pharm Inc |
Inhibidores de proteina quinasa biciclicos
|
CN103214484B
(zh)
|
2005-12-13 |
2016-07-06 |
因塞特控股公司 |
作为两面神激酶抑制剂的杂芳基取代的吡咯并[2,3-b]吡啶和吡咯并[2,3-b]嘧啶
|
JP5474354B2
(ja)
|
2005-12-30 |
2014-04-16 |
アステックス、セラピューティックス、リミテッド |
医薬化合物
|
WO2007106503A2
(en)
|
2006-03-13 |
2007-09-20 |
Osi Pharmaceuticals, Inc. |
Combined treatment with an egfr kinase inhibitor and an agent that sensitizes tumor cells to the effects of egfr kinase inhibitors
|
SI2526934T1
(sl)
|
2006-09-22 |
2016-04-29 |
Pharmacyclics Llc |
Inhibitorji Bruton tirozin kinaze
|
KR101566840B1
(ko)
|
2007-03-12 |
2015-11-06 |
와이엠 바이오사이언시즈 오스트레일리아 피티와이 엘티디 |
페닐 아미노 피리미딘 화합물 및 이의 용도
|
EA017389B1
(ru)
|
2007-03-23 |
2012-12-28 |
Амген Инк. |
Гетероциклические соединения и их применение
|
US8809273B2
(en)
|
2007-03-28 |
2014-08-19 |
Pharmacyclics, Inc. |
Inhibitors of Bruton's tyrosine kinase
|
EP2561875A3
(en)
|
2007-03-28 |
2013-06-12 |
Pharmacyclics, Inc. |
Inhibitors of bruton's tyrosine kinase
|
JP2010529193A
(ja)
|
2007-06-11 |
2010-08-26 |
ミイカナ セラピューティクス インコーポレイテッド |
置換ピラゾール化合物
|
EP2740731B1
(en)
|
2007-06-13 |
2016-03-23 |
Incyte Holdings Corporation |
Crystalline salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile
|
CL2008001709A1
(es)
|
2007-06-13 |
2008-11-03 |
Incyte Corp |
Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras.
|
RU2010128239A
(ru)
|
2007-12-13 |
2012-01-20 |
Новартис АГ (CH) |
Комбинации терапевтических средств, предназначенных для лечения рака
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
SI2288610T1
(sl)
|
2008-03-11 |
2016-11-30 |
Incyte Holdings Corporation |
Derivati azetidina in ciklobutana kot inhibitorji jak
|
TWI546290B
(zh)
|
2008-06-27 |
2016-08-21 |
賽基艾維洛米斯研究股份有限公司 |
雜芳基化合物及其用途
|
US9095592B2
(en)
|
2008-11-07 |
2015-08-04 |
The Research Foundation For The State University Of New York |
Bruton's tyrosine kinase as anti-cancer drug target
|
WO2010062848A1
(en)
|
2008-11-26 |
2010-06-03 |
Mikana Therapeutics, Inc. |
Substituted pyrazole compounds
|
US20100160322A1
(en)
|
2008-12-04 |
2010-06-24 |
Abbott Laboratories |
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
|
US8557983B2
(en)
|
2008-12-04 |
2013-10-15 |
Abbvie Inc. |
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
|
US8586754B2
(en)
|
2008-12-05 |
2013-11-19 |
Abbvie Inc. |
BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
|
US8563735B2
(en)
|
2008-12-05 |
2013-10-22 |
Abbvie Inc. |
Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
|
PA8851101A1
(es)
|
2008-12-16 |
2010-07-27 |
Lilly Co Eli |
Compuesto amino pirazol
|
JOP20190231A1
(ar)
|
2009-01-15 |
2017-06-16 |
Incyte Corp |
طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
|
RU2538965C2
(ru)
|
2009-01-19 |
2015-01-10 |
Эббви Инк. |
Вызывающие апоптоз средства для лечения рака и иммунных и аутоиммунных заболеваний
|
RU2535217C2
(ru)
|
2009-02-06 |
2014-12-10 |
Ниппон Синяку Ко., Лтд. |
Производные аминопиразина и лекарственные средства
|
PT2401267E
(pt)
|
2009-02-27 |
2014-04-10 |
Ambit Biosciences Corp |
Derivados de quinazolina moduladores de quinase jak e sua utilização em métodos
|
EP2424368B1
(en)
|
2009-04-29 |
2014-12-31 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
HUE046493T2
(hu)
|
2009-05-22 |
2020-03-30 |
Incyte Holdings Corp |
3-[4-(7H-Pirrolo[2,3-d]pirimidin-4-il)-lH-pirazol-l-il]oktán- vagy heptán-nitril JAK inhibitorokként
|
US8546399B2
(en)
|
2009-05-26 |
2013-10-01 |
Abbvie Inc. |
Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
|
SG10201704742YA
(en)
|
2009-05-26 |
2017-07-28 |
Abbvie Ireland Unlimited Co |
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
|
US9034875B2
(en)
|
2009-05-26 |
2015-05-19 |
Abbvie Inc. |
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
|
US20120157500A1
(en)
|
2009-08-24 |
2012-06-21 |
Weikang Tao |
Jak inhibition blocks rna interference associated toxicities
|
SI2473510T1
(sl)
|
2009-09-03 |
2014-10-30 |
Bristol-Myers Squibb Company |
Jak2 inhibitorji in njihova uporaba za zdravljenje mieloproliferativnih bolezni in raka
|
PL2486041T3
(pl)
|
2009-10-09 |
2014-01-31 |
Incyte Holdings Corp |
Pochodne hydroksylowe, keto i glukuronidowe 3-(4-(7H-pirolo[2,3-d]pirymidyn-4-ylo)-1H-pirazol-1-ilo)-3-cyklopentylopropanonitrylu
|
WO2011095556A1
(en)
|
2010-02-08 |
2011-08-11 |
N.V. Organon |
8-methyl-1-phenyl-imidazol[1,5-a]pyrazine compounds
|
UY33288A
(es)
|
2010-03-25 |
2011-10-31 |
Glaxosmithkline Llc |
Derivados de indolina inhibidores de la proteina quinasa r del reticulo endoplasmatico
|
CN103002738A
(zh)
|
2010-05-21 |
2013-03-27 |
英特利凯恩有限责任公司 |
用于激酶调节的化学化合物、组合物和方法
|
TWI535716B
(zh)
|
2010-05-31 |
2016-06-01 |
Ono Pharmaceutical Co |
Purine ketone derivatives
|
MX342405B
(es)
|
2010-06-03 |
2016-09-28 |
Pharmacyclics Inc |
El uso de inhibidores de la tirosina quinasa de bruton (btk).
|
US20120053189A1
(en)
|
2010-06-28 |
2012-03-01 |
Pharmacyclics, Inc. |
Btk inhibitors for the treatment of immune mediated conditions
|
BR112013003388A2
(pt)
|
2010-08-10 |
2016-07-12 |
Celgene Avilomics Res Inc |
sal de besilato de um inibidor de btk
|
WO2012020786A1
(ja)
|
2010-08-11 |
2012-02-16 |
日本新薬株式会社 |
医薬組成物
|
WO2012020787A1
(ja)
|
2010-08-11 |
2012-02-16 |
日本新薬株式会社 |
悪性リンパ腫治療剤
|
US20130296363A1
(en)
|
2010-09-01 |
2013-11-07 |
Ambit Biosciences Corporation |
Quinoline and isoquinoline derivatives for use as jak modulators
|
WO2012030917A1
(en)
|
2010-09-01 |
2012-03-08 |
Ambit Biosciences Corporation |
An optically active pyrazolylaminoquinazoline, and pharmaceutical compositions and methods of use thereof
|
US20130225614A1
(en)
|
2010-09-01 |
2013-08-29 |
Ambit Biosciences Corporation |
4-azolylaminoquinazoline derivatives and methods of use thereof
|
UA113500C2
(xx)
|
2010-10-29 |
2017-02-10 |
|
Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб
|
MX349533B
(es)
|
2010-10-29 |
2017-08-02 |
Abbvie Inc |
Dispersiones solidas que contienen un agente inductor de apoptosis.
|
EP2640384A1
(en)
|
2010-11-18 |
2013-09-25 |
Synta Pharmaceuticals Corp. |
Preselection of subjects for therapeutic treatment with oxygen sensitive agents based on hypoxic status
|
JP2014503499A
(ja)
|
2010-11-18 |
2014-02-13 |
シンタ ファーマスーティカルズ コーポレーション |
低酸素状態に基づく治療に適した被験体の事前選択
|
CN107266435A
(zh)
|
2010-11-23 |
2017-10-20 |
Abbvie 公司 |
细胞凋亡诱导剂的盐和晶形
|
JP5876067B2
(ja)
|
2010-11-23 |
2016-03-02 |
アッヴィ・バハマズ・リミテッド |
選択的bcl−2阻害薬を用いた処置方法
|
NZ611654A
(en)
|
2010-12-03 |
2015-08-28 |
Ym Biosciences Australia Pty |
Treatment of jak2-mediated conditions
|
PE20141303A1
(es)
|
2011-01-10 |
2014-10-01 |
Infinity Pharmaceuticals Inc |
Procedimiento para preparar isoquinolinonas y formas solidas de isoquinolinonas
|
CN103391779A
(zh)
|
2011-02-24 |
2013-11-13 |
辛塔医药品有限公司 |
使用hsp90抑制性化合物的***癌治疗
|
US20140045908A1
(en)
|
2011-02-25 |
2014-02-13 |
Synta Pharmaceuticals Corp. |
Hsp90 inhibitory compounds in treating jak/stat signaling-mediated cancers
|
AU2012239791B2
(en)
|
2011-04-04 |
2016-09-08 |
Gb005, Inc. |
Protein kinase inhibitors
|
CA2760174A1
(en)
|
2011-12-01 |
2013-06-01 |
Pharmascience Inc. |
Protein kinase inhibitors and uses thereof
|
WO2012155063A1
(en)
|
2011-05-11 |
2012-11-15 |
Synta Pharmaceuticals Corp. |
Treating cancer with an hsp90 inhibitory compound
|
US9580427B2
(en)
|
2011-05-17 |
2017-02-28 |
The Regents Of The University Of California |
Kinase inhibitors
|
EP2714039A1
(en)
|
2011-05-23 |
2014-04-09 |
Synta Pharmaceuticals Corp. |
Combination therapy of hsp90 inhibitory compounds with mek inhibitors
|
WO2012162372A1
(en)
|
2011-05-24 |
2012-11-29 |
Synta Pharmaceuticals Corp. |
Combination therapy of hsp90 inhibitory compounds with mtor/p13k inhibitors
|
EP2714033A1
(en)
|
2011-05-26 |
2014-04-09 |
Synta Pharmaceuticals Corp. |
Combination therapy of hsp90 inhibitory compounds with chk inhibitors
|
WO2013003629A2
(en)
|
2011-06-28 |
2013-01-03 |
Pharmacyclics, Inc. |
Methods and compositions for inhibition of bone resorption
|
JP2014520808A
(ja)
|
2011-07-07 |
2014-08-25 |
シンタ ファーマシューティカルズ コーポレーション |
Hsp90阻害化合物を用いた癌の治療
|
BR112014000653A2
(pt)
|
2011-07-13 |
2017-02-14 |
Pharmacyclics Inc |
inibidores de tirosina quinase de bruton
|
CA2842190A1
(en)
|
2011-07-19 |
2013-01-24 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
DK2734522T3
(en)
|
2011-07-19 |
2019-02-18 |
Merck Sharp & Dohme |
4-IMIDAZOPYRIDAZIN-1-YL-BENZAMIDES AND 4-IMIDAZOTRIAZIN-1-YL-BENZAMIDES AS BTK INHIBITORS
|
JP2014522860A
(ja)
|
2011-07-19 |
2014-09-08 |
メルク・シャープ・アンド・ドーム・ベー・フェー |
Btk阻害剤としての4−イミダゾピリダジン−1−イル−ベンズアミドおよび4−イミダゾトリアジン−1−イル−ベンズアミド
|
EP2548877A1
(en)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
|
JP6027610B2
(ja)
|
2011-07-19 |
2016-11-16 |
インフィニティー ファーマシューティカルズ, インコーポレイテッド |
複素環式化合物及びその使用
|
CA2844809A1
(en)
|
2011-08-19 |
2013-02-28 |
Synta Pharmaceuticals Corp. |
Combination cancer therapy of hsp90 inhibitor with antimetabolite
|
US8785470B2
(en)
|
2011-08-29 |
2014-07-22 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
JP6506555B2
(ja)
|
2011-10-19 |
2019-04-24 |
ファーマサイクリックス エルエルシー |
ブルトン型チロシンキナーゼ(Btk)阻害剤の使用
|
US8628752B2
(en)
|
2011-10-28 |
2014-01-14 |
Synta Pharmaceuticals Corp. |
Methods of identifying HSP90 inhibitors with less ocular toxicity
|
JP2014534228A
(ja)
|
2011-11-02 |
2014-12-18 |
シンタ ファーマシューティカルズ コーポレーション |
白金含有剤とhsp90阻害剤の組合せ療法
|
EP2773345A1
(en)
|
2011-11-02 |
2014-09-10 |
Synta Pharmaceuticals Corp. |
Cancer therapy using a combination of hsp90 inhibitors with topoisomerase i inhibitors
|
WO2013074594A1
(en)
|
2011-11-14 |
2013-05-23 |
Synta Pharmaceuticals Corp. |
Combination therapy of hsp90 inhibitors with braf inhibitors
|
KR20180034705A
(ko)
|
2011-11-29 |
2018-04-04 |
오노 야꾸힝 고교 가부시키가이샤 |
퓨리논 유도체 염산염
|
US20140212425A1
(en)
|
2011-12-05 |
2014-07-31 |
Immunomedics, Inc. |
Therapeutic use of anti-cd22 antibodies for inducing trogocytosis
|
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
|
US8940742B2
(en)
|
2012-04-10 |
2015-01-27 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
US20140079636A1
(en)
|
2012-04-16 |
2014-03-20 |
Dinesh U. Chimmanamada |
Targeted therapeutics
|
CA2871540A1
(en)
|
2012-05-10 |
2013-11-14 |
Synta Pharmaceuticals Corp. |
Treating cancer with hsp90 inhibitory compounds
|
WO2013170182A1
(en)
|
2012-05-11 |
2013-11-14 |
Synta Pharmaceuticals Corp. |
Treating cancer with an hsp90 inhibitory compound
|
AU2013262914A1
(en)
|
2012-05-16 |
2014-11-06 |
Synta Pharmaceuticals Corp. |
Pre-selection of subjects for therapeutic treatment with an Hsp90 inhibitor based on hypoxic status
|
LT3495367T
(lt)
|
2012-06-13 |
2021-02-25 |
Incyte Holdings Corporation |
Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai
|
US8828998B2
(en)
|
2012-06-25 |
2014-09-09 |
Infinity Pharmaceuticals, Inc. |
Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
|
AU2013302519B2
(en)
|
2012-08-17 |
2017-11-02 |
Concert Pharmaceuticals, Inc. |
Deuterated baricitinib
|
CN111437386A
(zh)
*
|
2012-09-07 |
2020-07-24 |
吉宁特有限公司 |
II型抗CD20抗体与选择性Bcl-2抑制剂的组合治疗
|
US9481682B2
(en)
|
2013-01-23 |
2016-11-01 |
Merck Sharp & Dohme Corp. |
Substituted benzamides and substituted pyridinecarboxamides as Btk inhibitors
|
CN105073115A
(zh)
|
2013-03-14 |
2015-11-18 |
药品循环有限责任公司 |
布鲁顿氏酪氨酸激酶抑制剂和cyp3a4抑制剂的组合
|
WO2014143807A2
(en)
|
2013-03-15 |
2014-09-18 |
Stromatt Scott |
Anti-cd37 antibody and bcr pathway antagonist combination therapy for treatment of b-cell malignancies and disorders
|
JP6575952B2
(ja)
*
|
2013-04-08 |
2019-09-18 |
ファーマサイクリックス エルエルシー |
イブルチニブ併用療法
|
DK2989106T3
(en)
|
2013-04-25 |
2017-03-20 |
Beigene Ltd |
CONDENSED HETEROCYCLIC COMPOUNDS AS PROTEINKINASE INHIBITORS
|
US20160113932A1
(en)
*
|
2013-05-30 |
2016-04-28 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using pi3 kinase isoform modulators
|
US20150005277A1
(en)
|
2013-06-28 |
2015-01-01 |
Beigene, Ltd. |
Protein Kinase Inhibitors and Uses Thereof
|
WO2015018522A1
(en)
|
2013-08-06 |
2015-02-12 |
Oncoethix Sa |
Bet-bromodomain inhibitor shows synergism with several anti-cancer agents in pre-clinical models of diffuse large b-cell lymphoma (dlbcl)
|
TWI660739B
(zh)
*
|
2013-10-25 |
2019-06-01 |
製藥公司 |
使用布魯頓氏酪胺酸激酶抑制劑之治療及免疫療法
|
US10328080B2
(en)
|
2013-12-05 |
2019-06-25 |
Acerta Pharma, B.V. |
Therapeutic combination of PI3K inhibitor and a BTK inhibitor
|
TW201613644A
(en)
|
2014-06-17 |
2016-04-16 |
Acerta Pharma Bv |
Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor, and/or a JAK-2 inhibitor
|
US9730938B2
(en)
|
2014-08-08 |
2017-08-15 |
Pharmacyclics Llc |
Bruton's tyrosine kinase inhibitor combinations and uses thereof
|
US20170224819A1
(en)
|
2014-08-11 |
2017-08-10 |
Acerta Pharma B.V. |
Therapeutic Combinations of a BTK Inhibitor, a PI3K Inhibitor, a JAK-2 Inhibitor, and/or a CDK 4/6 Inhibitor
|
HRP20211813T1
(hr)
*
|
2014-08-11 |
2022-03-04 |
Acerta Pharma B.V. |
Terapeutske kombinacije inhibitora btk i inhibitora bcl-2
|
TW201618774A
(zh)
*
|
2014-08-11 |
2016-06-01 |
艾森塔製藥公司 |
使用btk抑制劑透過調變腫瘤微環境來治療實體腫瘤及其他疾病之方法
|
LT3179992T
(lt)
*
|
2014-08-11 |
2022-06-27 |
Acerta Pharma B.V. |
Btk inhibitoriaus, pd-1 inhibitoriaus ir (arba) pd-l1 inhibitoriaus terapiniai deriniai
|
US9717745B2
(en)
*
|
2015-03-19 |
2017-08-01 |
Zhejiang DTRM Biopharma Co. Ltd. |
Pharmaceutical compositions and their use for treatment of cancer and autoimmune diseases
|
ES2895802T3
(es)
*
|
2015-07-02 |
2022-02-22 |
Acerta Pharma Bv |
Formas sólidas y formulaciones de (S)-4-(8-amino-3-(1-(but-2-inoil)pirrolidin-2-il)imidazo[1,5-a]pirazin-1-il)-N-(piridin-2-il)benzamida
|
US20170071962A1
(en)
*
|
2015-09-11 |
2017-03-16 |
Acerta Pharma B.V. |
Therapeutic Combinations of a Proteasome Inhibitor and a BTK Inhibitor
|
MA46285A
(fr)
*
|
2016-09-19 |
2019-07-31 |
Mei Pharma Inc |
Polythérapie
|
WO2018134786A1
(en)
*
|
2017-01-19 |
2018-07-26 |
Acerta Pharma B.V. |
Compositions and methods for the assessment of drug target occupancy for bruton's tyrosine kinase
|