Menin Inhibition With Revumenib for KMT2A -Rearranged Relapsed or Refractory Acute Leukemia (AUGMENT-101)
The University of Texas MD Anderson Cancer Center · City Of Hope National Medical Center · +25 more institutions
Abstract
PURPOSE Revumenib, an oral, small molecule inhibitor of the menin-lysine methyltransferase 2A (KMT2A) interaction, showed promising efficacy and safety in a phase I study of heavily pretreated patients with KMT2A -rearranged ( KMT2Ar ) acute leukemia. Here, we evaluated the activity of revumenib in individuals with relapsed/refractory (R/R) KMT2Ar acute leukemia. METHODS AUGMENT-101 is a phase I/II, open-label, dose-escalation and expansion study of revumenib conducted across 22 clinical sites in five countries (ClinicalTrials.gov identifier: NCT04065399 ). We report results from the phase II, registration-enabling portion. Individuals age ≥30 days with R/R KMT2Ar acute leukemia or with AML and nucleophosmin 1…
Citation impact
- FWCI
- 69.39
- Percentile
- 100%
- References
- 23
Authors
62Topics & keywords
- Augment
- Medicine
- Refractory (planetary science)
- Leukemia
- Cancer research
- Oncology
- Internal medicine
- Biology
- Good health and well-being
Funding
- AAmgen
- BSBristol-Myers Squibb
- ELEli Lilly and Company
- AAstraZeneca
- YUYale University
- GSGilead Sciences
- CCelgene
- CMCarnegie Mellon University
- FTFoghorn Therapeutics
- APAgios Pharmaceuticals
- CBCTI Biopharma
- IIncyte
- CBCalithera Biosciences
- SPSyndax Pharmaceuticals
- EEisai
- APAstellas Pharma
- GPGenesis Pharma
- SServier
- OPOno Pharmaceutical
- GGenentech
- DSDaiichi Sankyo Europe