GB0018891D0
(en)
*
|
2000-08-01 |
2000-09-20 |
Novartis Ag |
Organic compounds
|
WO2003057214A1
(en)
|
2001-12-28 |
2003-07-17 |
Somatocor Pharmaceuticals, Inc. |
Imidazolidin-2,4-dione derivatives as non-peptide somatostatin receptor ligands
|
DE60331770D1
(de)
*
|
2002-12-12 |
2010-04-29 |
Novartis Ag |
Prozess für die herstellung von peptiden, die eine 4-hydorxy-prolin substruktur enthalten
|
GB0229020D0
(en)
*
|
2002-12-12 |
2003-01-15 |
Novartis Ag |
Organic compounds
|
GB0300095D0
(en)
*
|
2003-01-03 |
2003-02-05 |
Novartis Ag |
Organic compounds
|
PE20050285A1
(es)
*
|
2003-06-24 |
2005-06-09 |
Novartis Ag |
Composicion farmaceutica que comprende analogos ciclicos de somatostatina
|
GB0314695D0
(en)
*
|
2003-06-24 |
2003-07-30 |
Novartis Ag |
Organic compounds
|
GB0318682D0
(en)
*
|
2003-08-08 |
2003-09-10 |
Novartis Ag |
Organic compounds
|
EP1522311A1
(fr)
|
2003-10-10 |
2005-04-13 |
Institut National De La Sante Et De La Recherche Medicale (Inserm) |
Utilisation de la somatostine ou d'un de ses analogues pour préparer un médicament destiné à réguler la réserve folliculaire ovarienne chez la femme non ménopausée
|
MY158342A
(en)
*
|
2003-11-14 |
2016-09-30 |
Novartis Ag |
Pharmaceutical composition
|
GB0412866D0
(en)
*
|
2004-06-09 |
2004-07-14 |
Novartis Ag |
Organic compounds
|
GB0428151D0
(en)
|
2004-12-22 |
2005-01-26 |
Novartis Ag |
Organic compounds
|
GB0602639D0
(en)
|
2006-02-09 |
2006-03-22 |
Novartis Ag |
Organic compounds
|
CN101460170A
(zh)
*
|
2006-06-08 |
2009-06-17 |
诺瓦提斯公司 |
促生长素抑制素类似物同多巴胺或同促生长素受体拮抗物的组合
|
US7697338B2
(en)
*
|
2006-11-16 |
2010-04-13 |
Sandisk Corporation |
Systems for controlled boosting in non-volatile memory soft programming
|
CN101553728B
(zh)
*
|
2006-11-28 |
2013-02-06 |
香港大学 |
颗粒体蛋白-上皮素前体(gep)抗体用于检测和抑制肝细胞癌(hcc)的用途
|
EP1941902A1
(en)
*
|
2007-01-02 |
2008-07-09 |
Novartis AG |
Use of Somatostatin analogs in cluster headache
|
CA2939778C
(en)
|
2007-01-31 |
2019-01-29 |
Dana-Farber Cancer Institute, Inc. |
Stabilized p53 peptides and uses thereof
|
CN101730708B
(zh)
|
2007-03-28 |
2013-09-18 |
哈佛大学校长及研究员协会 |
缝合多肽
|
AR066677A1
(es)
|
2007-05-24 |
2009-09-02 |
Novartis Ag |
Formulacion de pasireotida. composicion farmaceutica para liberacion prolongada. microparticulas.
|
WO2009009035A1
(en)
*
|
2007-07-06 |
2009-01-15 |
Ipsen Pharma S.A.S. |
Somatostatin analog and uses thereof
|
GB0719818D0
(en)
*
|
2007-10-11 |
2007-11-21 |
Asterion Ltd |
Growth hormone fusion polypeptides
|
PT2224947E
(pt)
*
|
2007-11-28 |
2015-06-24 |
Novartis Ag |
Utilização de análogos de somatostatina em meningioma
|
DK2225271T3
(da)
*
|
2007-12-03 |
2013-10-07 |
Italfarmaco Spa |
Nye ikke-selektive somatostatin-analoger
|
EP2067786A1
(en)
|
2007-12-07 |
2009-06-10 |
ITALFARMACO S.p.A. |
Novel non selective analogs of somatostatin
|
US20090325863A1
(en)
*
|
2008-06-13 |
2009-12-31 |
Kleinberg David L |
Somatostatin analogs and IGF-I inhibition for breast cancer prevention
|
EP2310042B1
(en)
|
2008-07-08 |
2012-12-05 |
Novartis AG |
Use of pasireotide for the treatment of endogenous hyperinsulinemic hypoglycemia
|
EP2172189A1
(en)
|
2008-10-01 |
2010-04-07 |
Novartis AG |
Pharmaceutical Compositions
|
EP2213307A1
(en)
|
2009-02-03 |
2010-08-04 |
Novartis AG |
Injectable depot formulations
|
AU2009294320B2
(en)
|
2008-09-17 |
2015-04-16 |
Amryt Endo, Inc. |
Pharmaceutical compositions and related methods of delivery
|
UY33236A
(es)
|
2010-02-25 |
2011-09-30 |
Novartis Ag |
Inhibidores dimericos de las iap
|
CA2807685C
(en)
|
2010-08-13 |
2020-10-06 |
Aileron Therapeutics, Inc. |
P53 derived peptidomimetic macrocycle
|
WO2012074559A2
(en)
|
2010-12-02 |
2012-06-07 |
New York University |
Treatment of non-proliferative cystic disease
|
UY33794A
(es)
|
2010-12-13 |
2012-07-31 |
Novartis Ag |
Inhibidores diméricos de las iap
|
JP2014501235A
(ja)
|
2010-12-13 |
2014-01-20 |
ノバルティス アーゲー |
二量体iap阻害剤
|
US20130035054A1
(en)
*
|
2011-07-14 |
2013-02-07 |
Faceon Mobile |
Phone with multi-portal access for display during incoming and outgoing call
|
US8835123B2
(en)
|
2011-08-02 |
2014-09-16 |
New York University |
Methods for detecting progenitor cells and uses thereof
|
EA025183B1
(ru)
|
2011-09-27 |
2016-11-30 |
Новартис Аг |
3-пиримидин-4-ил-оксазолидин-2-оны в качестве ингибиторов мутантной idh
|
TWI643868B
(zh)
|
2011-10-18 |
2018-12-11 |
艾利倫治療公司 |
擬肽巨環化合物
|
ES2629188T3
(es)
|
2011-12-05 |
2017-08-07 |
Camurus Ab |
Formulaciones peptídicas robustas de liberación controlada
|
WO2013084138A1
(en)
|
2011-12-05 |
2013-06-13 |
Novartis Ag |
Cyclic urea derivatives as androgen receptor antagonists
|
AU2013208720A1
(en)
|
2012-01-09 |
2014-07-24 |
Arrowhead Research Corporation |
RNAi agents to treat Beta-Catenin related diseases
|
US8815926B2
(en)
|
2012-01-26 |
2014-08-26 |
Novartis Ag |
Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases
|
CA2864120A1
(en)
|
2012-02-15 |
2013-08-22 |
Aileron Therapeutics, Inc. |
Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles
|
CA2862038C
(en)
|
2012-02-15 |
2021-05-25 |
Aileron Therapeutics, Inc. |
Peptidomimetic macrocycles
|
IN2014DN09831A
(enrdf_load_stackoverflow)
*
|
2012-05-25 |
2015-08-07 |
Camurus Ab |
|
TWI633887B
(zh)
|
2012-05-31 |
2018-09-01 |
大塚製藥股份有限公司 |
用於預防及/或治療多囊性腎臟病之藥物
|
CA2887285A1
(en)
|
2012-11-01 |
2014-05-08 |
Aileron Therapeutics, Inc. |
Disubstituted amino acids and methods of preparation and use thereof
|
US9480759B2
(en)
|
2012-11-21 |
2016-11-01 |
Serene, Llc |
Tin-117m somatostatin receptor binding compounds and methods
|
DK2958907T3
(en)
|
2013-02-19 |
2018-06-06 |
Novartis Ag |
Thus, benzothiophene derivatives and compositions as selective estrogen receptor degraders
|
CN105263929B
(zh)
|
2013-03-14 |
2018-08-28 |
诺华股份有限公司 |
作为突变idh抑制剂的3-嘧啶-4-基-噁唑烷-2-酮化合物
|
CA2903176A1
(en)
|
2013-03-14 |
2014-09-18 |
Novartis Ag |
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
|
WO2014147586A1
(en)
|
2013-03-22 |
2014-09-25 |
Novartis Ag |
1-(2-(ethylamino)pyrimidin-4-yl)pyrrolidin-2-ones as inhibitors of mutant idh
|
CN103467575B
(zh)
*
|
2013-08-22 |
2016-03-02 |
深圳翰宇药业股份有限公司 |
一种帕西瑞肽的制备方法
|
CN103641894B
(zh)
*
|
2013-12-06 |
2015-10-28 |
深圳翰宇药业股份有限公司 |
一种治疗库欣病的多肽药物的制备方法
|
WO2015092634A1
(en)
|
2013-12-16 |
2015-06-25 |
Novartis Ag |
1,2,3,4-tetrahydroisoquinoline compounds and compositions as selective estrogen receptor antagonists and degraders
|
KR20160098258A
(ko)
|
2013-12-19 |
2016-08-18 |
노파르티스 아게 |
약물 전달 시스템
|
JO3517B1
(ar)
|
2014-01-17 |
2020-07-05 |
Novartis Ag |
ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
|
ES2699354T3
(es)
|
2014-01-17 |
2019-02-08 |
Novartis Ag |
Derivados de 1-(triazin-3-il/piridazin-3-il)-piper(-azin)idina y composiciones de las mismas para inhibir la actividad de SHP2
|
EP3094627B1
(en)
|
2014-01-17 |
2018-08-22 |
Novartis AG |
1-pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and and compositions thereof for inhibiting the activity of shp2
|
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
|
WO2015138920A1
(en)
|
2014-03-14 |
2015-09-17 |
Novartis Ag |
Antibody molecules to lag-3 and uses thereof
|
AU2015265607A1
(en)
|
2014-05-28 |
2016-11-17 |
Idenix Pharmaceuticals Llc |
Nucleoside derivatives for the treatment of cancer
|
CN112245565A
(zh)
|
2014-09-24 |
2021-01-22 |
艾瑞朗医疗公司 |
拟肽大环化合物及其用途
|
MA41044A
(fr)
|
2014-10-08 |
2017-08-15 |
Novartis Ag |
Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer
|
AU2015333687B2
(en)
|
2014-10-14 |
2021-03-18 |
Dana-Farber Cancer Institute, Inc. |
Antibody molecules to PD-L1 and uses thereof
|
EP3226688B1
(en)
|
2014-12-05 |
2020-07-01 |
Merck Sharp & Dohme Corp. |
Tricyclic compounds as inhibitors of mutant idh enzymes
|
WO2016089830A1
(en)
|
2014-12-05 |
2016-06-09 |
Merck Sharp & Dohme Corp. |
Novel tricyclic compounds as inhibitors of mutant idh enzymes
|
US10086000B2
(en)
|
2014-12-05 |
2018-10-02 |
Merck Sharp & Dohme Corp. |
Tricyclic compounds as inhibitors of mutant IDH enzymes
|
EP3229824A4
(en)
|
2014-12-10 |
2018-07-11 |
Chiasma Inc. |
Oral octreotide administered in combination with other therapeutic agents
|
US20210317161A1
(en)
*
|
2014-12-19 |
2021-10-14 |
Auro Peptides Ltd |
A process for the preparation of pasireotide
|
WO2016100882A1
(en)
|
2014-12-19 |
2016-06-23 |
Novartis Ag |
Combination therapies
|
PT3253401T
(pt)
|
2015-02-03 |
2025-06-04 |
Amryt Endo Inc |
Tratamento da acromegalia com octreotida oral
|
MY190404A
(en)
|
2015-03-10 |
2022-04-21 |
Aduro Biotech Inc |
Compositions and methods for activating "stimulator of interferon gene"-dependent signalling
|
CA2979847A1
(en)
|
2015-03-20 |
2016-09-29 |
Aileron Therapeutics, Inc. |
Peptidomimetic macrocycles and uses thereof
|
EP3280723B1
(en)
*
|
2015-04-08 |
2021-01-06 |
Polyphor AG |
Backbone-cyclized peptidomimetics
|
WO2016189055A1
(en)
|
2015-05-27 |
2016-12-01 |
Idenix Pharmaceuticals Llc |
Nucleotides for the treatment of cancer
|
WO2016203404A1
(en)
|
2015-06-19 |
2016-12-22 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of shp2
|
ES2805232T3
(es)
|
2015-06-19 |
2021-02-11 |
Novartis Ag |
Compuestos y composiciones para inhibir la actividad de SHP2
|
JP6878316B2
(ja)
|
2015-06-19 |
2021-05-26 |
ノバルティス アーゲー |
Shp2の活性を阻害するための化合物および組成物
|
WO2016207912A1
(en)
*
|
2015-06-22 |
2016-12-29 |
Biophore India Pharmaceuticals Pvt. Ltd. |
Novel process for the preparation of pasireotide
|
GB201511790D0
(en)
|
2015-07-06 |
2015-08-19 |
Iomet Pharma Ltd |
Pharmaceutical compound
|
PT3317301T
(pt)
|
2015-07-29 |
2021-07-09 |
Novartis Ag |
Terapias de associação compreendendo moléculas de anticorpo contra lag-3
|
EP3878465A1
(en)
|
2015-07-29 |
2021-09-15 |
Novartis AG |
Combination therapies comprising antibody molecules to tim-3
|
EP3328418A1
(en)
|
2015-07-29 |
2018-06-06 |
Novartis AG |
Combination therapies comprising antibody molecules to pd-1
|
JP6596146B2
(ja)
|
2015-08-13 |
2019-10-23 |
メルク・シャープ・アンド・ドーム・コーポレーション |
Stingアゴニストとしての環状ジヌクレオチド化合物
|
US11453697B1
(en)
|
2015-08-13 |
2022-09-27 |
Merck Sharp & Dohme Llc |
Cyclic di-nucleotide compounds as sting agonists
|
JP2019500892A
(ja)
|
2015-11-03 |
2019-01-17 |
ヤンセン バイオテツク,インコーポレーテツド |
Tim−3に特異的に結合する抗体及びその使用
|
EP3389783B1
(en)
|
2015-12-15 |
2024-07-03 |
Merck Sharp & Dohme LLC |
Novel compounds as indoleamine 2,3-dioxygenase inhibitors
|
JP2019503349A
(ja)
|
2015-12-17 |
2019-02-07 |
ノバルティス アーゲー |
Pd−1に対する抗体分子およびその使用
|
US10577362B2
(en)
|
2016-05-04 |
2020-03-03 |
Genoscience Pharma |
Substituted 2, 4-diamino-quinoline derivatives for use in the treatment of proliferative diseases
|
EP3468972B1
(en)
|
2016-06-14 |
2020-05-20 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of shp2
|
US11098077B2
(en)
|
2016-07-05 |
2021-08-24 |
Chinook Therapeutics, Inc. |
Locked nucleic acid cyclic dinucleotide compounds and uses thereof
|
HUE056502T2
(hu)
|
2016-10-04 |
2022-02-28 |
Merck Sharp & Dohme |
Benzo[b]tiofén vegyületek mint STING agonisták
|
EP3541825A1
(en)
|
2016-11-21 |
2019-09-25 |
Idenix Pharmaceuticals LLC. |
Cyclic phosphate substituted nucleoside derivatives for the treatment of liver diseases
|
EP3573718B1
(en)
|
2017-01-27 |
2022-06-01 |
Janssen Biotech, Inc. |
Cyclic dinucleotides as sting agonists
|
AU2018212787B2
(en)
|
2017-01-27 |
2023-10-26 |
Janssen Biotech, Inc. |
Cyclic dinucleotides as sting agonists
|
UY37695A
(es)
|
2017-04-28 |
2018-11-30 |
Novartis Ag |
Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo
|
US11466047B2
(en)
|
2017-05-12 |
2022-10-11 |
Merck Sharp & Dohme Llc |
Cyclic di-nucleotide compounds as sting agonists
|
EP3642240A1
(en)
|
2017-06-22 |
2020-04-29 |
Novartis AG |
Antibody molecules to cd73 and uses thereof
|
RU2020109328A
(ru)
|
2017-08-04 |
2021-09-06 |
Мерк Шарп И Доум Корп. |
Комбинации антагонистов pd-1 и бензо[b]тиофеновых агонистов sting для лечения рака
|
JP2020530838A
(ja)
|
2017-08-04 |
2020-10-29 |
メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. |
がん治療のためのベンゾ[b]チオフェンSTINGアゴニスト
|
CA3074304A1
(en)
|
2017-09-11 |
2019-03-14 |
Krouzon Pharmaceuticals, Inc. |
Octahydrocyclopenta[c]pyrrole allosteric inhibitors of shp2
|
WO2019067332A1
(en)
|
2017-09-27 |
2019-04-04 |
Merck Sharp & Dohme Corp. |
COMPOSITIONS AND METHODS FOR TREATING CANCER THROUGH A COMBINATION OF PROGRAMMED DEATH ANTIBODY ANTIBODIES (PD-1) AND A CXCR2 ANTAGONIST
|
WO2019078968A2
(en)
*
|
2017-10-18 |
2019-04-25 |
Angex Pharmaceutical, Inc. |
CYCLIC COMPOUNDS AS IMMUNOMODULATORS
|
US12275729B2
(en)
|
2017-11-01 |
2025-04-15 |
Merck Sharp & Dohme Llc |
Substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
|
CA3082108A1
(en)
|
2017-11-14 |
2019-05-23 |
Merck Sharp & Dohme Corp. |
Novel substituted biaryl compounds as indoleamine 2,3-dioxygenase (ido) inhibitors
|
WO2019099294A1
(en)
|
2017-11-14 |
2019-05-23 |
Merck Sharp & Dohme Corp. |
Novel substituted biaryl compounds as indoleamine 2,3-dioxygenase (ido) inhibitors
|
WO2019118839A1
(en)
|
2017-12-15 |
2019-06-20 |
Janssen Biotech, Inc. |
Cyclic dinucleotides as sting agonists
|
EP3727401A4
(en)
|
2017-12-20 |
2022-04-06 |
Merck Sharp & Dohme Corp. |
CYCLIC DI-NUCLEOTIDE COMPOUNDS AS STING AGONISTS
|
US12398209B2
(en)
|
2018-01-22 |
2025-08-26 |
Janssen Biotech, Inc. |
Methods of treating cancers with antagonistic anti-PD-1 antibodies
|
US12215116B2
(en)
|
2018-03-13 |
2025-02-04 |
Merck Sharp & Dohme Llc |
Arginase inhibitors and methods of use
|
US11702430B2
(en)
|
2018-04-03 |
2023-07-18 |
Merck Sharp & Dohme Llc |
Aza-benzothiophene compounds as STING agonists
|
MA52189A
(fr)
|
2018-04-03 |
2021-02-17 |
Merck Sharp & Dohme |
Benzothiophènes et composés associés utilisés en tant qu'agonistes de sting
|
UY38247A
(es)
|
2018-05-30 |
2019-12-31 |
Novartis Ag |
Anticuerpos frente a entpd2, terapias de combinación y métodos de uso de los anticuerpos y las terapias de combinación
|
US11352320B2
(en)
|
2018-05-31 |
2022-06-07 |
Merck Sharp & Dohme Corp. |
Substituted [1.1.1] bicyclo compounds as indoleamine 2,3-dioxygenase inhibitors
|
US11274111B2
(en)
|
2018-06-20 |
2022-03-15 |
Merck Sharp & Dohme Corp. |
Arginase inhibitors and methods of use
|
US10596278B2
(en)
|
2018-07-25 |
2020-03-24 |
Advanced Accelerator Applications (Italy) S.R.L. |
Stable, concentrated radionuclide complex solutions
|
US10596276B2
(en)
|
2018-07-25 |
2020-03-24 |
Advanced Accelerator Applications (Italy) S.R.L. |
Stable, concentrated radionuclide complex solutions
|
TW202517302A
(zh)
|
2018-07-25 |
2025-05-01 |
法商高級催化劑應用品有限公司 |
穩定的、濃縮的放射性核種錯合物溶液
|
MX2021003158A
(es)
|
2018-09-18 |
2021-07-16 |
Nikang Therapeutics Inc |
Derivados de anillo tricíclico condensado como inhibidores de la fosfatasa de homología a src 2.
|
CN113382986A
(zh)
|
2018-09-25 |
2021-09-10 |
黑钻治疗公司 |
酪氨酸激酶抑制剂组合物、其制备方法和使用方法
|
US20220041613A1
(en)
|
2018-09-25 |
2022-02-10 |
Black Diamond Therapeutics, Inc. |
Tyrosine kinase inhibitor compositions, methods of making and methods of use
|
JP2022502385A
(ja)
|
2018-09-29 |
2022-01-11 |
ノバルティス アーゲー |
Shp2の活性を阻害するための化合物の製造方法
|
US12091405B2
(en)
|
2018-11-01 |
2024-09-17 |
Merck Sharp & Dohme Llc |
Substituted pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors
|
WO2020096871A1
(en)
|
2018-11-06 |
2020-05-14 |
Merck Sharp & Dohme Corp. |
Novel substituted tricyclic compounds as indoleamine 2,3-dioxygenase inhibitors
|
US12264134B2
(en)
|
2018-11-28 |
2025-04-01 |
Merck Sharp & Dohme Llc |
Substituted piperazine amide compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
|
WO2020131598A1
(en)
|
2018-12-18 |
2020-06-25 |
Merck Sharp & Dohme Corp. |
Arginase inhibitors and methods of use
|
EP3946324B1
(en)
|
2019-04-04 |
2025-07-30 |
Merck Sharp & Dohme LLC |
Inhibitors of histone deacetylase-3 useful for the treatment of cancer, inflammation, neurodegeneration diseases and diabetes
|
WO2020260547A1
(en)
|
2019-06-27 |
2020-12-30 |
Rigontec Gmbh |
Design method for optimized rig-i ligands
|
EP4007758A1
(en)
|
2019-08-02 |
2022-06-08 |
Mersana Therapeutics, Inc. |
Bis-[n-((5-carbamoyl)-1h-benzo[d]imidazol-2-yl)-pyrazol-5-carboxamide] derivatives and related compounds as sting (stimulator of interferon genes) agonists for the treatment of cancer
|
KR20220047810A
(ko)
|
2019-08-15 |
2022-04-19 |
블랙 다이아몬드 테라퓨틱스, 인코포레이티드 |
알키닐 퀴나졸린 화합물
|
CN114502590A
(zh)
|
2019-09-18 |
2022-05-13 |
诺华股份有限公司 |
Entpd2抗体、组合疗法、以及使用这些抗体和组合疗法的方法
|
PH12022551030A1
(en)
|
2019-10-28 |
2023-04-24 |
Shanghai Inst Materia Medica Cas |
Five-membered heterocyclic oxocarboxylic acid compound and medical use thereof
|
EP4069683A1
(en)
|
2019-12-06 |
2022-10-12 |
Mersana Therapeutics, Inc. |
Dimeric compounds as sting agonists
|
WO2021126725A1
(en)
|
2019-12-17 |
2021-06-24 |
Merck Sharp & Dohme Corp. |
Novel substituted 1,3,8-triazaspiro[4,5]decane-2,4-dione compounds as indoleamine 2,3-dioxygenase (ido) and/or tryptophan 2,3-dioxygenase (tdo) inhibitors
|
EP4087583A4
(en)
|
2020-01-07 |
2024-01-24 |
Merck Sharp & Dohme LLC |
ARGINASE INHIBITORS AND METHODS OF USE
|
WO2021195206A1
(en)
|
2020-03-24 |
2021-09-30 |
Black Diamond Therapeutics, Inc. |
Polymorphic forms and related uses
|
IL297859A
(en)
|
2020-04-02 |
2023-01-01 |
Mersana Therapeutics Inc |
Antibody drug conjugates comprising sting agonists
|
WO2021226003A1
(en)
|
2020-05-06 |
2021-11-11 |
Merck Sharp & Dohme Corp. |
Il4i1 inhibitors and methods of use
|
WO2022140472A1
(en)
|
2020-12-22 |
2022-06-30 |
Nikang Therapeutics, Inc. |
Compounds for degrading cyclin-dependent kinase 2 via ubiquitin proteosome pathway
|
US11141457B1
(en)
|
2020-12-28 |
2021-10-12 |
Amryt Endo, Inc. |
Oral octreotide therapy and contraceptive methods
|
AU2022207648A1
(en)
|
2021-01-13 |
2023-07-27 |
Monte Rosa Therapeutics Ag |
Isoindolinone compounds
|
WO2022170052A1
(en)
|
2021-02-05 |
2022-08-11 |
Black Diamond Therapeutics, Inc. |
Quinazoline derivatives, pyridopyrimidine derivatives, pyrimidopyrimidine derivatives, and uses thereof
|
EP4323350A1
(en)
|
2021-04-14 |
2024-02-21 |
Monte Rosa Therapeutics AG |
Isoindolinone compounds
|
WO2022219412A1
(en)
|
2021-04-14 |
2022-10-20 |
Monte Rosa Therapeutics Ag |
Isoindolinone amide compounds useful to treat diseases associated with gspt1
|
WO2022227015A1
(en)
|
2021-04-30 |
2022-11-03 |
Merck Sharp & Dohme Corp. |
Il4i1 inhibitors and methods of use
|
CN117980310A
(zh)
|
2021-07-14 |
2024-05-03 |
尼坎治疗公司 |
作为kras抑制剂的亚烷基衍生物
|
CN119053595A
(zh)
|
2022-03-28 |
2024-11-29 |
尼坎治疗公司 |
作为细胞周期蛋白依赖性激酶2抑制剂的磺酰氨基衍生物
|
EP4536363A1
(en)
|
2022-06-08 |
2025-04-16 |
Nikang Therapeutics, Inc. |
Sulfamide derivatives as cyclin-dependent kinase 2 inhibitors
|
EP4580686A1
(en)
*
|
2022-08-30 |
2025-07-09 |
Grafton Therapeutics Sàrl |
Halogenated somatostatin analogs with multiple somatostatin receptor subtype selectivity
|
CN120152967A
(zh)
|
2022-11-11 |
2025-06-13 |
霖康疗法公司 |
用于经由泛素蛋白酶体途径降解细胞周期蛋白依赖性激酶2的含有2,5-取代的嘧啶衍生物的双功能化合物
|
US20240336608A1
(en)
|
2023-03-29 |
2024-10-10 |
Merck Sharp & Dohme Llc |
Il4i1 inhibitors and methods of use
|
WO2025072462A1
(en)
|
2023-09-27 |
2025-04-03 |
Nikang Therapeutics, Inc. |
Sulfonamide derivatives as cyclin-dependent kinase 2 inhibitors
|
WO2025117616A1
(en)
|
2023-11-27 |
2025-06-05 |
Nikang Therapeutics, Inc. |
Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and cyclin-dependent kinase 4 via ubiquitin proteasome pathway
|
WO2025117981A1
(en)
|
2023-12-02 |
2025-06-05 |
Nikang Therapeutics, Inc. |
Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway
|