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NCT06917911 · ClinicalTrials.gov registry record · Phase 2

Testing the Addition of Venetoclax or Gemtuzumab Ozogamicin (GO) to Usual Treatment Regimen (Cytarabine and Daunorubicin, "7+3") for Core Binding Factor Acute Myeloid Leukemia (CBF-AML) to Improve Response (A MYELOMATCH Treatment Trial)

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Recruiting
Registry status
Phase 2
Development phase
162
Enrollment target

NCT06917911: Recruiting Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT06917911 is a Phase 2 study that is actively recruiting participants, run by National Cancer Institute (NCI). The registered enrollment target is 162 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (22% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT06917911, a Phase 2 study, is actively recruiting participants, sponsored by National Cancer Institute (NCI).

RECRUITING
Registry status
Phase 2
Development phase
162 participants
Enrollment target

Study Summary

This phase II MYELOMATCH treatment trial compares the effect of venetoclax to gemtuzumab ozogamicin, when given with cytarabine and daunorubicin ("7+3" regimen), for the treatment of patients with core binding factor acute myeloid leukemia (CBF-AML). 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. Gemtuzumab ozogamicin is a monoclonal antibody, called gemtuzumab, linked to an antitumor antibiotic drug, called ozogamicin. Gemtuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as CD33 receptors, and delivers ozogamicin to kill them. Chemotherapy drugs, such as cytarabine and daunorubicin work in different ways to stop the growth of cancer cells either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving venetoclax with cytarabine and daunorubicin may have fewer side effects and be as effective or better than the combination with gemtuzumab ozogamicin in treating patients with core binding factor AML.

Primary Outcome

MRD will be evaluated by Molecular Diagnostics Network flow cytometry and will be defined at a threshold of ≤ 10\^-3.

Interventions

  • PROCEDURE Biospecimen Collection
  • PROCEDURE Bone Marrow Aspiration
  • PROCEDURE Bone Marrow Biopsy
  • DRUG Cytarabine
  • DRUG Daunorubicin Hydrochloride

Trial Details

FieldValue
Enrollment Target 162 participants
Start Date 2027-02-02
Est. Completion 2027-11-25
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What NCT06917911 shows while recruiting

NCT06917911 is an interventional study that assigns participants to a tested intervention. The registered 162 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (22% higher).

The record links to 0 conditions, and to 5 interventions - of which Biospecimen Collection is the first listed.

NCT06917911 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06917911 about?

NCT06917911 is a clinical study titled "Testing the Addition of Venetoclax or Gemtuzumab Ozogamicin (GO) to Usual Treatment Regimen (Cytarabine and Daunorubicin, "7+3") for Core Binding Factor Acute Myeloid Leukemia (CBF-AML) to Improve Response (A MYELOMATCH Treatment Trial)". This phase II MYELOMATCH treatment trial compares the effect of venetoclax to gemtuzumab ozogamicin, when given with cytarabine and daunorubicin ("7+3" regimen), for the treatment of patients with core binding factor acute myeloid leukemia (CBF-AML). Venetoclax is in a class of medications called B-...

What is the current status of trial NCT06917911?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 162 participants. The study started on 2027-02-02. Estimated completion is 2027-11-25.

What interventions are being tested in trial NCT06917911?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Bone Marrow Aspiration (PROCEDURE), Bone Marrow Biopsy (PROCEDURE), Cytarabine (DRUG), Daunorubicin Hydrochloride (DRUG).

Who is sponsoring clinical trial NCT06917911?

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

How this trial's enrollment target compares

Where NCT06917911's enrollment target sits among peer trials

162 418th of 2000 higher than 1,579 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT06917911, the US trial registry maintained by the National Library of Medicine. NCT06917911 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.