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NCT06317649 · ClinicalTrials.gov registry record · Phase 2

Venetoclax and HMA Treatment of Older and Unfit Adults With FLT3 Mutated Acute Myeloid Leukemia (AML) (A MyeloMATCH Treatment Trial)

A Phase 2 study of Acute Myeloid Leukemia, sponsored by National Cancer Institute (NCI).

Recruiting
Registry status
Phase 2
Development phase
147
Enrollment target
20
Study locations

NCT06317649: Recruiting Phase 2 study of Acute Myeloid Leukemia, sponsored by National Cancer Institute (NCI).

NCT06317649 is a Phase 2 study of Acute Myeloid Leukemia that is actively recruiting participants, run by National Cancer Institute (NCI). The registered enrollment target is 147 participants, above the 115-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (28% higher). The trial reports 20 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06317649, a Phase 2 study of Acute Myeloid Leukemia, is actively recruiting participants, sponsored by National Cancer Institute (NCI).

RECRUITING
Registry status
Phase 2
Development phase
147 participants
Enrollment target
20
Study locations

Study Summary

This phase II MyeloMATCH treatment trial compares the usual treatment of azacitidine and venetoclax to the combination treatment of azacitidine, venetoclax and gilteritinib in treating older and unfit patients with acute myeloid leukemia and FLT3 mutations. Azacitidine is a drug that is absorbed into DNA and leads to the activation of cancer suppressor genes, which are genes that help control cell growth. Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival. Gilteritinib is in a class of medications called kinase inhibitors. It works by blocking the action of a certain naturally occurring substance that may be needed to help cancer cells multiply. This study may help doctors find out if these different approaches are better than the usual approaches. To decide if they are better, the study doctors are looking to see if the study drugs lead to a higher percentage of patients achieving a deeper remission compared to the usual approach.

Primary Outcome

Will be assessed by multiparameter flow cytometry at a level of ≤ 1 residual blast / 1,000 leukocytes (≤ 10\^-3). Patients achieved MRD negative CR at any time up to 4 cycles will count as a responder. The MRD negative CR frequencies will be compared between each triplet regimen and the control regimen using Fisher's exact test with one-sided alpha of 0.05 for each comparison. Test results with one-sided p-value \< 0.05 will be considered statistically significant.

Conditions Studied

Interventions

  • PROCEDURE Biospecimen Collection
  • PROCEDURE Bone Marrow Aspiration
  • PROCEDURE Bone Marrow Biopsy
  • DRUG Azacitidine
  • DRUG Gilteritinib

Study Locations (20)

California

  • Alta Bates Summit Medical Center-Herrick Campus - Berkeley
  • Kaiser Permanente Dublin - Dublin
  • Kaiser Permanente-Fremont - Fremont
  • Kaiser Permanente Fresno Orchard Plaza - Fresno
  • Kaiser Permanente-Fresno - Fresno
  • Cedars Sinai Medical Center - Los Angeles
  • Kaiser Permanente- Modesto MOB II - Modesto
  • Kaiser Permanente-Modesto - Modesto
  • Kaiser Permanente-Oakland - Oakland
  • Kaiser Permanente-Roseville - Roseville
  • Kaiser Permanente Downtown Commons - Sacramento
  • University of California Davis Comprehensive Cancer Center - Sacramento
  • Kaiser Permanente-South Sacramento - Sacramento
  • Kaiser Permanente-San Francisco - San Francisco
  • UCSF Medical Center-Parnassus - San Francisco
  • Kaiser Permanente-Santa Teresa-San Jose - San Jose
  • Kaiser Permanente San Leandro - San Leandro

Arizona

  • Banner University Medical Center - Tucson - Tucson
  • University of Arizona Cancer Center-North Campus - Tucson

Arkansas

  • University of Arkansas for Medical Sciences - Little Rock

Trial Details

FieldValue
Enrollment Target 147 participants
Start Date 2024-09-27
Est. Completion 2029-05-15
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What NCT06317649 shows while recruiting

NCT06317649 is an interventional study that assigns participants to a tested intervention. The registered 147 participants enrollment target is mid-sized for trials with a published cap, above the 115-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (28% higher).

The record links to 1 condition, with Acute Myeloid Leukemia appearing as the primary indexed condition, and to 5 interventions - of which Biospecimen Collection is the first listed.

NCT06317649 names 20 study sites across 3 states, led by California, Arizona, Arkansas.

Frequently Asked Questions

What is clinical trial NCT06317649 about?

NCT06317649 is a clinical study titled "Venetoclax and HMA Treatment of Older and Unfit Adults With FLT3 Mutated Acute Myeloid Leukemia (AML) (A MyeloMATCH Treatment Trial)". This phase II MyeloMATCH treatment trial compares the usual treatment of azacitidine and venetoclax to the combination treatment of azacitidine, venetoclax and gilteritinib in treating older and unfit patients with acute myeloid leukemia and FLT3 mutations. Azacitidine is a drug that is absorbed int...

What is the current status of trial NCT06317649?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 147 participants. The study started on 2024-09-27. Estimated completion is 2029-05-15.

What conditions does trial NCT06317649 study?

This clinical trial studies the following conditions: Acute Myeloid Leukemia.

What interventions are being tested in trial NCT06317649?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Bone Marrow Aspiration (PROCEDURE), Bone Marrow Biopsy (PROCEDURE), Azacitidine (DRUG), Gilteritinib (DRUG).

Who is sponsoring clinical trial NCT06317649?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06317649 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Acute Myeloid Leukemia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06317649's enrollment target sits among peer trials

147 58th of 306 higher than 249 of 306 other Acute Myeloid Leukemia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Acute Myeloid Leukemia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06317649, the US trial registry maintained by the National Library of Medicine. NCT06317649 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.