drugset / Trial / NCT04065399

A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 Mutation

NCT04065399 ↗

Phase 1/2 Recruiting 447 enrolled Syndax Pharmaceuticals
NaSequentialOpen-labelTreatment

Summary

Phase 1 dose escalation will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of revumenib in participants with acute leukemia. In Phase 2, participants will be enrolled in 4 indication-specific expansion cohorts to determine the efficacy, short- and long-term safety, and tolerability of revumenib.

Timeline

Start
2019-11-05
Primary completion
2027-12-15
Completion
2027-12-15

Outcome

Met primary endpoint

paper In the efficacy-evaluable patients (n = 57), the CR + CRh rate was 22.8% (95% CI, 12.7 to 35.8), exceeding the null hypothesis of 10% (P = .0036). PMID 39121437 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Revumenib Small molecule 95 mg/m2 Oral
Subject Revumenib Small molecule 163 mg Oral
Background Cobicistat Small molecule 150 mg —