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
|
ATE461173T1
(en)
*
|
2002-12-12 |
2010-04-15 |
Novartis Pharma Gmbh |
PROCESS FOR THE PRODUCTION OF PEPTIDES CONTAINING A 4-HYDORXY-PROLINE SUBSTRUCTURE
|
GB0300095D0
(en)
*
|
2003-01-03 |
2003-02-05 |
Novartis Ag |
Organic compounds
|
AR044852A1
(en)
*
|
2003-06-24 |
2005-10-05 |
Novartis Ag |
A PHARMACEUTICAL COMPOSITION FOR PARENTERAL ADMINISTRATION THAT INCLUDES A SOMATOSTATINE ANALOG
|
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
(en)
|
2003-10-10 |
2005-04-13 |
Institut National De La Sante Et De La Recherche Medicale (Inserm) |
Use of somatostatin or analogs thereof for the preparation of a medicament for the regulation of ovarian follicles reserve by non menopausaled women
|
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
|
RU2008151727A
(en)
*
|
2006-06-08 |
2010-07-20 |
Новартис АГ (CH) |
COMBINATION OF SOMATOSTATIN ANALOGUES WITH DOPAMINE RECEPTOR OR GROWTH HORMONE RECEPTOR ANTAGONIST
|
US7697338B2
(en)
*
|
2006-11-16 |
2010-04-13 |
Sandisk Corporation |
Systems for controlled boosting in non-volatile memory soft programming
|
CN101553728B
(en)
*
|
2006-11-28 |
2013-02-06 |
香港大学 |
Use of granulin-epithelin precursor (GEP) antibodies for detection and inhibition of hepatocellular carcinoma (HCC)
|
EP1941902A1
(en)
*
|
2007-01-02 |
2008-07-09 |
Novartis AG |
Use of Somatostatin analogs in cluster headache
|
JP5649825B2
(en)
|
2007-01-31 |
2015-01-07 |
デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド |
Stabilized p53 peptides and methods of use thereof
|
KR20160061439A
(en)
|
2007-03-28 |
2016-05-31 |
프레지던트 앤드 펠로우즈 오브 하바드 칼리지 |
Stitched polypeptides
|
PE20090387A1
(en)
|
2007-05-24 |
2009-04-28 |
Novartis Ag |
PASSIREOTY FORMULATION
|
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
|
RU2523416C2
(en)
*
|
2007-11-28 |
2014-07-20 |
Новартис Аг |
Using somatostatin analogues in meningioma
|
EP2067786A1
(en)
|
2007-12-07 |
2009-06-10 |
ITALFARMACO S.p.A. |
Novel non selective analogs of somatostatin
|
SI2225271T1
(en)
|
2007-12-03 |
2013-10-30 |
Italfarmaco S.P.A. |
New non-selective somatostatin analogues
|
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
|
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
|
HUE033611T2
(en)
|
2008-09-17 |
2017-12-28 |
Chiasma Inc |
Pharmaceutical compositions and related methods of delivery
|
UY33236A
(en)
|
2010-02-25 |
2011-09-30 |
Novartis Ag |
DIMERIC INHIBITORS OF THE IAP
|
ES2711526T3
(en)
|
2010-08-13 |
2019-05-06 |
Aileron Therapeutics Inc |
Peptidomimetic macrocycles
|
US8629103B2
(en)
|
2010-12-02 |
2014-01-14 |
New York University |
Treatment of non-proliferative cystic disease of the breast
|
UY33794A
(en)
|
2010-12-13 |
2012-07-31 |
Novartis Ag |
DIMERIC INHIBITORS OF THE IAP
|
EP2651917A1
(en)
|
2010-12-13 |
2013-10-23 |
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
|
WO2013019923A2
(en)
|
2011-08-02 |
2013-02-07 |
New York University |
Methods for detecting progenitor cells and uses thereof
|
SG11201400989TA
(en)
|
2011-09-27 |
2014-04-28 |
Novartis Ag |
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
|
JP6342808B2
(en)
|
2011-10-18 |
2018-06-13 |
エイルロン セラピューティクス,インコーポレイテッド |
Peptidomimetic macrocycle
|
US20140329858A1
(en)
|
2011-12-05 |
2014-11-06 |
Novartis Ag |
Cyclic Urea Derivatives As Androgen Receptor Antagonists
|
PE20141297A1
(en)
|
2011-12-05 |
2014-10-09 |
Camurus Ab |
ROBUST PEPTIDIC FORMULATIONS OF CONTROLLED RELEASE
|
CN104302768A
(en)
|
2012-01-09 |
2015-01-21 |
诺华股份有限公司 |
Organic composition for treating 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
|
RU2017145921A
(en)
|
2012-02-15 |
2019-02-21 |
Эйлерон Терапьютикс, Инк. |
PEPTIDOMIMETIC MACROCYCLES
|
CN104144695A
(en)
|
2012-02-15 |
2014-11-12 |
爱勒让治疗公司 |
Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles
|
PE20150195A1
(en)
*
|
2012-05-25 |
2015-02-27 |
Camarus Ab |
SOMATOSTATIN RECEPTOR AGONIST FORMULATIONS
|
TWI633887B
(en)
|
2012-05-31 |
2018-09-01 |
大塚製藥股份有限公司 |
Drug for preventing and/or treating polycystic kidney disease
|
AU2013337388B2
(en)
|
2012-11-01 |
2018-08-02 |
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
|
MX2015012822A
(en)
|
2013-03-14 |
2016-05-31 |
Novartis Ag |
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh.
|
CN105263929B
(en)
|
2013-03-14 |
2018-08-28 |
诺华股份有限公司 |
3-Pyrimidin-4-yl-oxazolidin-2-one compounds as mutant IDH inhibitors
|
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
(en)
*
|
2013-08-22 |
2016-03-02 |
深圳翰宇药业股份有限公司 |
A kind of preparation method of Pa Xirui peptide
|
CN103641894B
(en)
*
|
2013-12-06 |
2015-10-28 |
深圳翰宇药业股份有限公司 |
A kind of preparation method treating the polypeptide drugs of hypercortisolism
|
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
|
AU2014369213B2
(en)
|
2013-12-19 |
2017-10-19 |
Novartis Ag |
Drug delivery systems
|
JP6523303B2
(en)
|
2014-01-17 |
2019-05-29 |
ノバルティス アーゲー |
1-Pyridazin / triazin-3-yl-piperazine / piperidine / pyrrolidine derivatives for inhibiting the activity of SHP2 and compositions thereof
|
JO3517B1
(en)
|
2014-01-17 |
2020-07-05 |
Novartis Ag |
N-azaspirocycloalkane substituted n-heteroaryl compounds and compositions for inhibiting the activity of shp2
|
WO2015107494A1
(en)
|
2014-01-17 |
2015-07-23 |
Novartis Ag |
1 -(triazin-3-yi_/pyridazin-3-yl)-piper(-azine)idine derivatives and compositions thereof for inhibiting the activity of shp2
|
JOP20200094A1
(en)
|
2014-01-24 |
2017-06-16 |
Dana Farber Cancer Inst Inc |
Antibody Molecules of PD-1 and Their Uses
|
JOP20200096A1
(en)
|
2014-01-31 |
2017-06-16 |
Children’S Medical Center Corp |
Antibody molecules to tim-3 and uses thereof
|
LT3116909T
(en)
|
2014-03-14 |
2020-02-10 |
Novartis Ag |
Antibody molecules to lag-3 and uses thereof
|
JP2017516779A
(en)
|
2014-05-28 |
2017-06-22 |
アイデニクス・ファーマシューティカルズ・エルエルシー |
Nucleoside derivatives for cancer treatment
|
CA2961258A1
(en)
|
2014-09-24 |
2016-03-31 |
Aileron Therapeutics, Inc. |
Peptidomimetic macrocycles and uses thereof
|
MA41044A
(en)
|
2014-10-08 |
2017-08-15 |
Novartis Ag |
COMPOSITIONS AND METHODS OF USE FOR INCREASED IMMUNE RESPONSE AND CANCER TREATMENT
|
PE20171067A1
(en)
|
2014-10-14 |
2017-07-24 |
Novartis Ag |
ANTIBODY MOLECULES BINDING AND USES OF PD-L1
|
WO2016089797A1
(en)
|
2014-12-05 |
2016-06-09 |
Merck Sharp & Dohme Corp. |
Novel tricyclic compounds as inhibitors of mutant idh enzymes
|
EP3226690B1
(en)
|
2014-12-05 |
2020-05-20 |
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
|
EP3229824A4
(en)
|
2014-12-10 |
2018-07-11 |
Chiasma Inc. |
Oral octreotide administered in combination with other therapeutic agents
|
EP3233918A1
(en)
|
2014-12-19 |
2017-10-25 |
Novartis AG |
Combination therapies
|
EP3233899B1
(en)
|
2014-12-19 |
2020-06-24 |
Auro Peptides LTD |
A process for the preparation of pasireotide
|
HK1247818A1
(en)
|
2015-02-03 |
2018-10-05 |
Amryt Endo, Inc. |
Method of treating diseases
|
TN2017000375A1
(en)
|
2015-03-10 |
2019-01-16 |
Aduro Biotech Inc |
Compositions and methods for activating "stimulator of interferon gene" -dependent signalling
|
CN107614003A
(en)
|
2015-03-20 |
2018-01-19 |
艾瑞朗医疗公司 |
Peptidomimetic macrocycles and uses thereof
|
US10730911B2
(en)
|
2015-04-08 |
2020-08-04 |
Universitat Zurich |
Backbone-cyclized peptidomimetics with GLP-1R modulating activity
|
EP3303361A1
(en)
|
2015-05-27 |
2018-04-11 |
Idenix Pharmaceuticals LLC |
Nucleotides for the treatment of cancer
|
ES2741746T3
(en)
|
2015-06-19 |
2020-02-12 |
Novartis Ag |
Compounds and compositions to inhibit SHP2 activity
|
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
|
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
|
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
|
DK3317301T3
(en)
|
2015-07-29 |
2021-06-28 |
Immutep Sas |
COMBINATION THERAPIES INCLUDING ANTIBODY MOLECULES AGAINST LAYER-3
|
US11453697B1
(en)
|
2015-08-13 |
2022-09-27 |
Merck Sharp & Dohme Llc |
Cyclic di-nucleotide compounds as sting agonists
|
GEP20207182B
(en)
|
2015-08-13 |
2020-11-25 |
Merck Sharp & Dohme |
Cyclic di-nucleotide compounds as sting agonists
|
CN114478790A
(en)
|
2015-11-03 |
2022-05-13 |
詹森生物科技公司 |
Antibodies that specifically bind to PD-1 and TIM-3 and uses thereof
|
WO2017106062A1
(en)
|
2015-12-15 |
2017-06-22 |
Merck Sharp & Dohme Corp. |
Novel compounds as indoleamine 2,3-dioxygenase inhibitors
|
KR102833068B1
(en)
|
2015-12-17 |
2025-07-14 |
노파르티스 아게 |
Antibody molecules against PD-1 and their uses
|
SI3452465T1
(en)
|
2016-05-04 |
2021-04-30 |
Genoscience Pharma |
Substituted 2, 4-diamino-quinoline derivatives for use in the treatment of proliferative diseases
|
MX383856B
(en)
|
2016-06-14 |
2025-03-14 |
Novartis Ag |
COMPOUNDS AND COMPOSITIONS FOR INHIBITING SHP2 ACTIVITY.
|
US11098077B2
(en)
|
2016-07-05 |
2021-08-24 |
Chinook Therapeutics, Inc. |
Locked nucleic acid cyclic dinucleotide compounds and uses thereof
|
JP6636673B2
(en)
|
2016-10-04 |
2020-01-29 |
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. |
Benzo [b] thiophene compounds as STING agonists
|
EP3541825A1
(en)
|
2016-11-21 |
2019-09-25 |
Idenix Pharmaceuticals LLC. |
Cyclic phosphate substituted nucleoside derivatives for the treatment of liver diseases
|
JP7275031B2
(en)
|
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 |
Cyclic dinucleotides as STING agonists
|
EP3573717B1
(en)
|
2017-01-27 |
2021-07-28 |
Janssen Biotech, Inc. |
Cyclic dinucleotides as sting agonists
|
UY37695A
(en)
|
2017-04-28 |
2018-11-30 |
Novartis Ag |
BIS 2’-5’-RR- (3’F-A) (3’F-A) CYCLE DINUCLEOTIDE COMPOUND AND USES OF THE SAME
|
US11466047B2
(en)
|
2017-05-12 |
2022-10-11 |
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
|
EP3661499A4
(en)
|
2017-08-04 |
2021-04-21 |
Merck Sharp & Dohme Corp. |
COMBINATIONS OF PD-1 ANTAGONISTS AND BENZO [B]
|
EP3661498A4
(en)
|
2017-08-04 |
2021-04-21 |
Merck Sharp & Dohme Corp. |
BENZO [B] THIOPHEN STING ANTAGONISTS FOR CANCER TREATMENT
|
TW202517628A
(en)
|
2017-09-11 |
2025-05-01 |
美商克魯松藥物公司 |
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 with a combination of programmed death receptor (pd-1) antibodies and a cxcr2 antagonist
|
US11180497B2
(en)
*
|
2017-10-18 |
2021-11-23 |
Angex Pharmaceutical, Inc. |
Cyclic compounds as immunomodulating agents
|
US12275729B2
(en)
|
2017-11-01 |
2025-04-15 |
Merck Sharp & Dohme Llc |
Substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
|
US11498904B2
(en)
|
2017-11-14 |
2022-11-15 |
Merck Sharp & Dohme Llc |
Substituted biaryl 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
|
MX2020006290A
(en)
|
2017-12-15 |
2020-12-03 |
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
|
EP3765006A4
(en)
|
2018-03-13 |
2022-02-23 |
Merck Sharp & Dohme Corp. |
Arginase inhibitors and methods of use
|
US11702430B2
(en)
|
2018-04-03 |
2023-07-18 |
Merck Sharp & Dohme Llc |
Aza-benzothiophene compounds as STING agonists
|
JP7326319B2
(en)
|
2018-04-03 |
2023-08-15 |
メルク・シャープ・アンド・ドーム・エルエルシー |
Benzothiophenes and Related Compounds as STING Agonists
|
TWI869346B
(en)
|
2018-05-30 |
2025-01-11 |
瑞士商諾華公司 |
Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies
|
WO2019231870A1
(en)
|
2018-05-31 |
2019-12-05 |
Merck Sharp & Dohme Corp. |
Novel substituted [1.1.1] bicyclo compounds as indoleamine 2,3-dioxygenase inhibitors
|
EP3810615A4
(en)
|
2018-06-20 |
2022-03-30 |
Merck Sharp & Dohme Corp. |
ARGINASE INHIBITORS AND METHODS OF USE
|
TW202517302A
(en)
|
2018-07-25 |
2025-05-01 |
法商高級催化劑應用品有限公司 |
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
|
US10596276B2
(en)
|
2018-07-25 |
2020-03-24 |
Advanced Accelerator Applications (Italy) S.R.L. |
Stable, concentrated radionuclide complex solutions
|
CN112996795B
(en)
|
2018-09-18 |
2024-11-12 |
尼坎治疗公司 |
Fused tricyclic derivatives as SRC homolog-2 phosphatase inhibitors
|
AU2019346550A1
(en)
|
2018-09-25 |
2021-04-22 |
Black Diamond Therapeutics, Inc. |
Quinazoline derivatives as tyrosine kinase inhibitor, compositions, methods of making them and their use
|
CN113164776A
(en)
|
2018-09-25 |
2021-07-23 |
黑钻治疗公司 |
Tyrosine kinase inhibitor compositions, methods of making and methods of using the same
|
WO2020065453A1
(en)
|
2018-09-29 |
2020-04-02 |
Novartis Ag |
Process of manufacture of a compound for inhibiting the activity of shp2
|
WO2020092183A1
(en)
|
2018-11-01 |
2020-05-07 |
Merck Sharp & Dohme Corp. |
Novel substituted pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors
|
US12065438B2
(en)
|
2018-11-06 |
2024-08-20 |
Merck Sharp & Dohme Llc |
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
|
WO2020205688A1
(en)
|
2019-04-04 |
2020-10-08 |
Merck Sharp & Dohme Corp. |
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
|
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(en)
|
2019-08-15 |
2025-02-07 |
黑钻治疗公司 |
Alkynylquinazoline compounds
|
US20220348651A1
(en)
|
2019-09-18 |
2022-11-03 |
Novartis Ag |
Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies
|
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
|
WO2021141751A1
(en)
|
2020-01-07 |
2021-07-15 |
Merck Sharp & Dohme Corp. |
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|
WO2021195206A1
(en)
|
2020-03-24 |
2021-09-30 |
Black Diamond Therapeutics, Inc. |
Polymorphic forms and related uses
|
KR20230004896A
(en)
|
2020-04-02 |
2023-01-06 |
메르사나 테라퓨틱스, 인코포레이티드 |
Antibody drug conjugates comprising sting agonists
|
IL297781A
(en)
|
2020-05-06 |
2022-12-01 |
Merck Sharp & Dohme Llc |
il4i1 inhibitors and methods of use
|
US20250018049A1
(en)
|
2020-12-22 |
2025-01-16 |
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
|
WO2022219407A1
(en)
|
2021-04-14 |
2022-10-20 |
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
|
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(en)
|
2021-04-30 |
2022-11-03 |
Merck Sharp & Dohme Corp. |
Il4i1 inhibitors and methods of use
|
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(en)
|
2021-07-14 |
2024-05-03 |
尼坎治疗公司 |
Alkylene derivatives as KRAS inhibitors
|
JP2025509886A
(en)
|
2022-03-28 |
2025-04-11 |
ニカング セラピューティクス, インコーポレイテッド |
Sulfonamide derivatives as cyclin-dependent kinase 2 inhibitors
|
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(en)
|
2022-06-08 |
2025-04-16 |
Nikang Therapeutics, Inc. |
Sulfamide derivatives as cyclin-dependent kinase 2 inhibitors
|
WO2024047112A1
(en)
*
|
2022-08-30 |
2024-03-07 |
Somtheranostics Sarl |
Halogenated somatostatin analogs with multiple somatostatin receptor subtype selectivity
|
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(en)
|
2022-11-11 |
2024-09-01 |
美商尼坎醫療公司 |
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|
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(en)
|
2023-03-29 |
2025-01-16 |
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|
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(en)
|
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|
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(en)
|
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|
WO2025117981A1
(en)
|
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Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway
|