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Completed Phase 1 Interventional

A Study of Revumenib in Combination With Chemotherapy in Participants With R/R Acute Leukemia

ClinicalTrials.gov ID: NCT05326516

Public ClinicalTrials.gov record NCT05326516. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 4:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

AUGMENT-102: A Phase 1, Open-label, Dose-escalation Study to Evaluate Safety, Tolerability and Preliminary Anti-Leukemic Activity of SNDX-5613 in Combination With Chemotherapy in Patients With Relapsed/Refractory Leukemias Harboring Alterations in KMT2A/MLL, Nucleophosmin 1 (NPM1), and Nucleoporin 98 (NUP98) Genes

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the safety and tolerability of revumenib when given in combination with 2 different chemotherapy regimens in participants with relapsed/refractory acute leukemias harboring KMT2A rearrangement, KMT2A amplification, NPM1c, or NUP98r.

Study identification

NCT ID
NCT05326516
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Syndax Pharmaceuticals
Industry
Enrollment
30 participants

Conditions and interventions

Eligibility (public fields only)

Age range
30 Days and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 9, 2022 (Actual)
Primary completion
Jul 29, 2024 (Actual)
Completion
Jul 29, 2024 (Actual)
Last update posted
Aug 13, 2024

2022 – 2024

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
University of California, San Francisco (UCSF) Benioff Children's Hospital San Francisco California 94158 —
Dana-Farber Cancer Institute Boston Massachusetts 02115 —
Children's Mercy Hospital Kansas City Missouri 64108 —
Washington University School of Medicine St Louis Missouri 63110 —
David H Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center New York New York 10021 —
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229 —
The Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 —
St. Jude Children's Research Hospital, Inc Memphis Tennessee 38105 —
MD Anderson Cancer Center Houston Texas 77030 —
Texas Children's Cancer and Hematology Center Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05326516, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 13, 2024 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05326516 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →