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Tazemetostat

Known as: N-((4,6-Dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-5-(ethyl(oxan-4-yl)amino)-4-methyl-4'-((morpholin-4-yl)methyl)(1,1'-biphenyl)-3-carboxamide 
An orally available, small molecule selective and S-adenosyl methionine (SAM) competitive inhibitor of histone methyl transferase EZH2, with… 
National Institutes of Health

Papers overview

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Review
2020
Review
2020
The submission was primarily based on updated phase II efficacy and safety data for tazemetostat for patients with relapsed or… 
2020
2020
The FDA granted accelerated approval of tazemetostat (Tazverik) based on data reported in a phase II clinical trial of the… 
2018
2018
Tazemetostat (EPZ-6438) is a potent, selective, orally bioavailable small molecule inhibitor of EZH2, the enzymatic subunit of… 
2018
2018
Tazemetostat has antitumor activity in B-cell non-Hodgkin lymphoma and advanced solid tumors. 
2017
2017
The EZH2 inhibitor tazemetostat (EPZ-6438) is currently being evaluated in phase 2 clinical trials for the treatment of non… 
2017
2017
The EZH2 inhibitor tazemetostat has shown good activity and is very well tolerated in an analysis of three trials of patients… 
2017
2017
Children with relapsed or refractory INI1-deficient malignant rhabdoid tumors, epithelioid sarcomas, or poorly differentiated… 
2016
2016
Tazemetostat is a selective oral small molecule inhibitor of enhancer of zeste homolog 2 (EZH2). In preclinical evaluations of… 
2016
2016
Tazemetostat is a small molecule inhibitor of the histone methyltransferase EZH2 and is currently in phase 2 clinical trials… 
2016
2016
Background: Tazemetostat is a selective oral small molecule inhibitor of enhancer of zeste homolog 2 (EZH2). Results from in…