Expanded Access Program for Revumenib

NCT05918913 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2025-09-05

No results posted yet for this study

Summary

This expanded access program will provide an investigational treatment option in a controlled clinical setting for participants who are not otherwise eligible to participate in other Syndax-sponsored clinical studies and have no approved treatment options.

Conditions

  • Relapsed/Refractory Acute Leukemia

Interventions

DRUG

Revumenib

Revumenib administered orally every 12 hours.

Sponsors & Collaborators

Principal Investigators

  • Medical Director · Syndax Pharmaceuticals

Eligibility

Min Age
6 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05918913 on ClinicalTrials.gov