|
GB0018891D0
(en)
*
|
2000-08-01 |
2000-09-20 |
Novartis Ag |
Organic compounds
|
|
US7189856B2
(en)
|
2001-12-28 |
2007-03-13 |
Gideon Shapiro |
Non-peptide somatostatin receptor ligands
|
|
GB0229020D0
(en)
*
|
2002-12-12 |
2003-01-15 |
Novartis Ag |
Organic compounds
|
|
JP4796303B2
(ja)
*
|
2002-12-12 |
2011-10-19 |
ノバルティス アーゲー |
4−ヒドロキシ−プロリン部分構造を含むペプチドの合成方法
|
|
GB0300095D0
(en)
*
|
2003-01-03 |
2003-02-05 |
Novartis Ag |
Organic compounds
|
|
GB0314695D0
(en)
*
|
2003-06-24 |
2003-07-30 |
Novartis Ag |
Organic compounds
|
|
AR044852A1
(es)
*
|
2003-06-24 |
2005-10-05 |
Novartis Ag |
Una composicion farmaceutica para la administracion parenteral que comprende un analogo de somatostatina
|
|
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
|
|
JP2009539803A
(ja)
*
|
2006-06-08 |
2009-11-19 |
ノバルティス アクチエンゲゼルシャフト |
ソマトスタチン−アナログとドーパミン−または成長ホルモン受容体アンタゴニストの組合せ剤
|
|
US7697338B2
(en)
*
|
2006-11-16 |
2010-04-13 |
Sandisk Corporation |
Systems for controlled boosting in non-volatile memory soft programming
|
|
WO2008064570A1
(en)
*
|
2006-11-28 |
2008-06-05 |
The University Of Hong Kong |
The use of granulin-epithelin precursor (gep) antibodies for detection and suppression of hepatocellular carcinoma (hcc)
|
|
EP1941902A1
(en)
*
|
2007-01-02 |
2008-07-09 |
Novartis AG |
Use of Somatostatin analogs in cluster headache
|
|
WO2008095063A1
(en)
|
2007-01-31 |
2008-08-07 |
Dana-Farber Cancer Institute, Inc. |
Stabilized p53 peptides and uses thereof
|
|
EP2508531B1
(en)
|
2007-03-28 |
2016-10-19 |
President and Fellows of Harvard College |
Stitched polypeptides
|
|
PE20090387A1
(es)
|
2007-05-24 |
2009-04-28 |
Novartis Ag |
Formulacion de pasireotida
|
|
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
|
|
PL2225271T3
(pl)
|
2007-12-03 |
2013-12-31 |
Italfarmaco Spa |
Nowe nieselektywne analogi somatostatyny
|
|
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
|
|
SI2310042T1
(sl)
*
|
2008-07-08 |
2013-03-29 |
Novartis Ag |
Uporaba pasireotida za zdravljenje endogene hiperinzulinemične hipoglikemije
|
|
EP2213307A1
(en)
|
2009-02-03 |
2010-08-04 |
Novartis AG |
Injectable depot formulations
|
|
EP2172189A1
(en)
|
2008-10-01 |
2010-04-07 |
Novartis AG |
Pharmaceutical Compositions
|
|
BRPI0918652B1
(pt)
|
2008-09-17 |
2021-10-19 |
Chiasma, Inc. |
Composição farmacêutica compreendendo um meio hidrofóbico e uma forma sólida que compreende polipeptídeo e sal de ácido graxo de cadeia média, processo de produção da mesma e forma de dosagem oral
|
|
UY33236A
(es)
|
2010-02-25 |
2011-09-30 |
Novartis Ag |
Inhibidores dimericos de las iap
|
|
CN103282510A
(zh)
|
2010-08-13 |
2013-09-04 |
爱勒让治疗公司 |
拟肽大环化合物
|
|
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
|
|
US20130266590A1
(en)
|
2010-12-13 |
2013-10-10 |
Novartis Ag |
Dimeric iap inhibitors
|
|
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
|
|
JP6026544B2
(ja)
|
2011-09-27 |
2016-11-16 |
ノバルティス アーゲー |
変異体idhの阻害剤としての3−ピリミジン−4−イル−オキサゾリジン−2−オン類
|
|
KR20140100937A
(ko)
|
2011-10-18 |
2014-08-18 |
에일러론 테라퓨틱스 인코포레이티드 |
펩티도미메틱 거대고리
|
|
CN104105479B
(zh)
|
2011-12-05 |
2018-04-10 |
卡穆鲁斯公司 |
鲁棒性控释制剂
|
|
KR20140098242A
(ko)
|
2011-12-05 |
2014-08-07 |
노파르티스 아게 |
안드로겐 수용체 길항제로서의 시클릭 우레아 유도체
|
|
AU2013208720A1
(en)
|
2012-01-09 |
2014-07-24 |
Arrowhead Research Corporation |
RNAi agents to treat Beta-Catenin related diseases
|
|
UY34591A
(es)
|
2012-01-26 |
2013-09-02 |
Novartis Ag |
Compuestos de imidazopirrolidinona
|
|
WO2013123266A1
(en)
|
2012-02-15 |
2013-08-22 |
Aileron Therapeutics, Inc. |
Peptidomimetic macrocycles
|
|
JP6450192B2
(ja)
|
2012-02-15 |
2019-01-09 |
エイルロン セラピューティクス,インコーポレイテッド |
トリアゾール架橋した、およびチオエーテル架橋したペプチドミメティック大環状化合物
|
|
SG11201407678YA
(en)
*
|
2012-05-25 |
2014-12-30 |
Camurus Ab |
Somatostatin receptor agonist formulations
|
|
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
|
|
WO2014071241A1
(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
|
|
EP3360870A1
(en)
|
2013-02-19 |
2018-08-15 |
Novartis AG |
Benzothiophene derivatives and compositions thereof as selective estrogen receptor degraders
|
|
MX355945B
(es)
|
2013-03-14 |
2018-05-07 |
Novartis Ag |
3-pirimidin-4-il-oxazolidin-2-onas como inhibidoras de idh mutante.
|
|
BR112015022483A2
(pt)
|
2013-03-14 |
2017-07-18 |
Novartis Ag |
3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante
|
|
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
|
|
CN105828803B
(zh)
|
2013-12-19 |
2019-06-07 |
诺华股份有限公司 |
药物递送系统
|
|
CN105899493B
(zh)
|
2014-01-17 |
2019-03-29 |
诺华股份有限公司 |
用于抑制shp2活性的1-(三嗪-3-基/哒嗪-3-基)-哌(-嗪)啶衍生物及其组合物
|
|
JO3517B1
(ar)
|
2014-01-17 |
2020-07-05 |
Novartis Ag |
ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط 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
|
|
PH12016501545B1
(en)
|
2014-03-14 |
2023-12-06 |
Immutep Sas |
Antibody molecules to lag-3 and uses thereof
|
|
CA2947939A1
(en)
|
2014-05-28 |
2015-12-03 |
Idenix Pharmaceuticals Llc |
Nucleoside derivatives for the treatment of cancer
|
|
SG11201702223UA
(en)
|
2014-09-24 |
2017-04-27 |
Aileron Therapeutics Inc |
Peptidomimetic macrocycles and uses thereof
|
|
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
|
|
CA2964367C
(en)
|
2014-10-14 |
2024-01-30 |
Novartis Ag |
Antibody molecules to pd-l1 and uses thereof
|
|
WO2016089833A1
(en)
|
2014-12-05 |
2016-06-09 |
Merck Sharp & Dohme Corp. |
Novel 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
|
|
WO2016089797A1
(en)
|
2014-12-05 |
2016-06-09 |
Merck Sharp & Dohme Corp. |
Novel tricyclic compounds as inhibitors of mutant idh enzymes
|
|
EP4321213A3
(en)
|
2014-12-10 |
2024-05-15 |
Amryt Endo, Inc. |
Oral octreotide administered in combination with other therapeutic agents
|
|
WO2016100882A1
(en)
|
2014-12-19 |
2016-06-23 |
Novartis Ag |
Combination therapies
|
|
EP3233899B1
(en)
|
2014-12-19 |
2020-06-24 |
Auro Peptides LTD |
A process for the preparation of pasireotide
|
|
HUE071943T2
(hu)
|
2015-02-03 |
2025-10-28 |
Amryt Endo Inc |
Akromegália kezelése oktreotid orális alkalmazásával
|
|
HK1248603A1
(zh)
|
2015-03-10 |
2018-10-19 |
Aduro Biotech, Inc. |
用於活化"干扰素基因的刺激剂"依懒性信号传导的组合物和方法
|
|
US10253067B2
(en)
|
2015-03-20 |
2019-04-09 |
Aileron Therapeutics, Inc. |
Peptidomimetic macrocycles and uses thereof
|
|
WO2016162127A1
(en)
*
|
2015-04-08 |
2016-10-13 |
Polyphor Ag |
Backbone-cyclized peptidomimetics
|
|
WO2016189055A1
(en)
|
2015-05-27 |
2016-12-01 |
Idenix Pharmaceuticals Llc |
Nucleotides for the treatment of cancer
|
|
WO2016203405A1
(en)
|
2015-06-19 |
2016-12-22 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of shp2
|
|
US10287266B2
(en)
|
2015-06-19 |
2019-05-14 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of SHP2
|
|
WO2016203404A1
(en)
|
2015-06-19 |
2016-12-22 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of shp2
|
|
US10556924B2
(en)
|
2015-06-22 |
2020-02-11 |
Biophore India Pharmaceuticals Pvt. Ltd. |
Process for the preparation of pasireotide
|
|
GB201511790D0
(en)
|
2015-07-06 |
2015-08-19 |
Iomet Pharma Ltd |
Pharmaceutical compound
|
|
DK3317301T3
(da)
|
2015-07-29 |
2021-06-28 |
Immutep Sas |
Kombinationsterapier omfattende antistofmolekyler mod lag-3
|
|
WO2017019897A1
(en)
|
2015-07-29 |
2017-02-02 |
Novartis Ag |
Combination therapies comprising antibody molecules to tim-3
|
|
EP4378957A3
(en)
|
2015-07-29 |
2024-08-07 |
Novartis AG |
Combination therapies comprising antibody molecules to pd-1
|
|
US11453697B1
(en)
|
2015-08-13 |
2022-09-27 |
Merck Sharp & Dohme Llc |
Cyclic di-nucleotide compounds as sting agonists
|
|
SG10202010609QA
(en)
|
2015-08-13 |
2020-11-27 |
Merck Sharp & Dohme |
Cyclic di-nucleotide compounds as sting agonists
|
|
JP2019500893A
(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 |
Pd−1及びtim−3に特異的に結合する抗体及びそれらの使用
|
|
WO2017106062A1
(en)
|
2015-12-15 |
2017-06-22 |
Merck Sharp & Dohme Corp. |
Novel compounds as indoleamine 2,3-dioxygenase inhibitors
|
|
KR102833068B1
(ko)
|
2015-12-17 |
2025-07-14 |
노파르티스 아게 |
Pd-1에 대한 항체 분자 및 그의 용도
|
|
CN109415343A
(zh)
|
2016-05-04 |
2019-03-01 |
基因科学医药公司 |
用于治疗增殖性疾病的取代的2,4-二氨基-喹啉衍生物
|
|
KR102457146B1
(ko)
|
2016-06-14 |
2022-10-19 |
노파르티스 아게 |
Shp2의 활성을 억제하기 위한 화합물 및 조성물
|
|
EP3507367A4
(en)
|
2016-07-05 |
2020-03-25 |
Aduro BioTech, Inc. |
CYCLIC DINUCLEOTID COMPOUNDS WITH INCLUDED NUCLEIC ACIDS AND USES THEREOF
|
|
MA46452B1
(fr)
|
2016-10-04 |
2021-10-29 |
Merck Sharp & Dohme |
Composés de benzo[b]thiophéne en tant qu'agonistes de sting
|
|
EP3541825A1
(en)
|
2016-11-21 |
2019-09-25 |
Idenix Pharmaceuticals LLC. |
Cyclic phosphate substituted nucleoside derivatives for the treatment of liver diseases
|
|
JP7275031B2
(ja)
|
2017-01-27 |
2023-05-17 |
ヤンセン バイオテツク,インコーポレーテツド |
Stingアゴニストとしての環状ジヌクレオチド
|
|
CN110234404A
(zh)
|
2017-01-27 |
2019-09-13 |
詹森生物科技公司 |
作为sting激动剂的环状二核苷酸
|
|
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
|
|
EP3621624B1
(en)
|
2017-05-12 |
2023-08-30 |
Merck Sharp & Dohme LLC |
Cyclic di-nucleotide compounds as sting agonists
|
|
WO2018237173A1
(en)
|
2017-06-22 |
2018-12-27 |
Novartis Ag |
Antibody molecules to cd73 and uses thereof
|
|
AU2018311965A1
(en)
|
2017-08-04 |
2020-02-13 |
Merck Sharp & Dohme Llc |
Combinations of PD-1 antagonists and benzo[b]thiophene sting antagonists for cancer treatment
|
|
CA3071538A1
(en)
|
2017-08-04 |
2019-02-07 |
Merck Sharp & Dohme Corp. |
Benzo[b]thiophene sting agonists for cancer treatment
|
|
US10435389B2
(en)
|
2017-09-11 |
2019-10-08 |
Krouzon Pharmaccuticals, 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
|
|
ES2948307T3
(es)
|
2017-11-14 |
2023-09-08 |
Merck Sharp & Dohme Llc |
Nuevos compuestos de biarilo sustituidos como inhibidores de indolamina 2,3-dioxigenasa (IDO)
|
|
US11498904B2
(en)
|
2017-11-14 |
2022-11-15 |
Merck Sharp & Dohme Llc |
Substituted biaryl compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
|
|
MX2020006290A
(es)
|
2017-12-15 |
2020-12-03 |
Janssen Biotech Inc |
Dinucleotidos ciclicos como agonistas de sting.
|
|
US11685761B2
(en)
|
2017-12-20 |
2023-06-27 |
Merck Sharp & Dohme Llc |
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
|
|
WO2019195063A1
(en)
|
2018-04-03 |
2019-10-10 |
Merck Sharp & Dohme Corp. |
Aza-benzothiophene compounds as sting agonists
|
|
KR102755259B1
(ko)
|
2018-04-03 |
2025-01-15 |
머크 샤프 앤드 돔 엘엘씨 |
Sting 효능제로서의 벤조티오펜 및 관련 화합물
|
|
US11542505B1
(en)
|
2018-04-20 |
2023-01-03 |
Merck Sharp & Dohme Llc |
Substituted RIG-I agonists: compositions and methods thereof
|
|
AR126019A1
(es)
|
2018-05-30 |
2023-09-06 |
Novartis Ag |
Anticuerpos frente a entpd2, terapias de combinación y métodos de uso de los anticuerpos y las terapias de combinación
|
|
EP3810116B1
(en)
|
2018-05-31 |
2023-11-15 |
Merck Sharp & Dohme LLC |
Novel 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
|
|
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
|
|
US10596276B2
(en)
|
2018-07-25 |
2020-03-24 |
Advanced Accelerator Applications (Italy) S.R.L. |
Stable, concentrated radionuclide complex solutions
|
|
US10596278B2
(en)
|
2018-07-25 |
2020-03-24 |
Advanced Accelerator Applications (Italy) S.R.L. |
Stable, concentrated radionuclide complex solutions
|
|
TWI827677B
(zh)
|
2018-09-18 |
2024-01-01 |
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|
|
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(ko)
|
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2021-11-17 |
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|
|
US20220041613A1
(en)
|
2018-09-25 |
2022-02-10 |
Black Diamond Therapeutics, Inc. |
Tyrosine kinase inhibitor compositions, methods of making and methods of use
|
|
CA3113379A1
(en)
|
2018-09-29 |
2020-04-02 |
Novartis Ag |
Process of manufacture of a compound for inhibiting the activity of shp2
|
|
EP3873464B1
(en)
|
2018-11-01 |
2025-07-30 |
Merck Sharp & Dohme LLC |
Novel substituted pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors
|
|
EP3877366B1
(en)
|
2018-11-06 |
2026-01-28 |
Merck Sharp & Dohme LLC |
Novel substituted tricyclic compounds as indoleamine 2,3-dioxygenase inhibitors
|
|
EP3886845B1
(en)
|
2018-11-28 |
2024-09-04 |
Merck Sharp & Dohme LLC |
Novel 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
|
|
EP3990635A1
(en)
|
2019-06-27 |
2022-05-04 |
Rigontec GmbH |
Design method for optimized rig-i ligands
|
|
JP2022543086A
(ja)
|
2019-08-02 |
2022-10-07 |
メルサナ セラピューティクス インコーポレイテッド |
がんの処置用のSTING(インターフェロン遺伝子刺激因子)アゴニストとしてのビス-[N-((5-カルバモイル)-1H-ベンゾ[d]イミダゾール-2-イル)-ピラゾール-5-カルボキサミド]誘導体および関連化合物
|
|
KR102910319B1
(ko)
|
2019-08-15 |
2026-01-09 |
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
|
|
US20230074558A1
(en)
|
2019-12-06 |
2023-03-09 |
Mersana Therapeutics, Inc. |
Dimeric compounds as sting agonists
|
|
US20220396577A1
(en)
|
2019-12-17 |
2022-12-15 |
Merck Sharp & Dohme Llc |
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
|
|
WO2021141751A1
(en)
|
2020-01-07 |
2021-07-15 |
Merck Sharp & Dohme Corp. |
Arginase inhibitors and methods of use
|
|
WO2021195206A1
(en)
|
2020-03-24 |
2021-09-30 |
Black Diamond Therapeutics, Inc. |
Polymorphic forms and related uses
|
|
JP2023520513A
(ja)
|
2020-04-02 |
2023-05-17 |
メルサナ セラピューティクス インコーポレイテッド |
Stingアゴニストを含む抗体薬物コンジュゲート
|
|
IL297781A
(en)
|
2020-05-06 |
2022-12-01 |
Merck Sharp & Dohme Llc |
il4i1 inhibitors and methods of use
|
|
EP4267575A1
(en)
|
2020-12-22 |
2023-11-01 |
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
|
|
JP2024504932A
(ja)
|
2021-01-13 |
2024-02-02 |
モンテ ローザ セラピューティクス, インコーポレイテッド |
イソインドリノン化合物
|
|
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
|
|
TW202317589A
(zh)
|
2021-07-14 |
2023-05-01 |
美商尼坎醫療公司 |
作為kras抑制劑的伸烷基衍生物
|
|
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(ko)
|
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2024-11-28 |
니캉 테라퓨틱스 인코포레이티드 |
사이클린 의존적 키나제 2 억제제로서의 설폰아미도 유도체
|
|
WO2023240024A1
(en)
|
2022-06-08 |
2023-12-14 |
Nikang Therapeutics, Inc. |
Sulfamide derivatives as cyclin-dependent kinase 2 inhibitors
|
|
JP2025528439A
(ja)
*
|
2022-08-30 |
2025-08-28 |
グラフトン セラピューティクス エスアエールエル |
複数のソマトスタチン受容体サブタイプ選択性を有するハロゲン化ソマトスタチン類似体
|
|
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(ja)
|
2022-11-11 |
2025-11-14 |
ニカング セラピューティクス, インコーポレイテッド |
ユビキチンプロテアソーム経路を介してサイクリン依存性キナーゼ2を分解するための2,5-置換ピリミジン誘導体を含有する二官能性化合物
|
|
WO2024206357A1
(en)
|
2023-03-29 |
2024-10-03 |
Merck Sharp & Dohme Llc |
Il4i1 inhibitors and methods of use
|
|
TW202502382A
(zh)
|
2023-06-30 |
2025-01-16 |
美商默沙東有限責任公司 |
治療組合及其用途和治療方法
|
|
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
|
|
WO2025212828A1
(en)
|
2024-04-03 |
2025-10-09 |
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
|
|
WO2025240536A1
(en)
|
2024-05-15 |
2025-11-20 |
Nikang Therapeutics, Inc. |
Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and/or cyclin-dependent kinase 4 via ubiquitin proteasome pathway
|