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Terminated Phase 2 Interventional Results available

A Study of MBG453 in Combination With Azacitidine and Venetoclax in AML Patients Unfit for Chemotherapy

ClinicalTrials.gov ID: NCT04150029

Public ClinicalTrials.gov record NCT04150029. 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 Sep 3, 2026, 1:16 PM EDT

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

Official title

A Phase II Multi-center, Single Arm, Safety and Efficacy Study of MBG453 in Combination With Azacitidine and Venetoclax for the Treatment of Acute Myeloid Leukemia (AML) in Adult Patients Unfit for Chemotherapy

Brief summary

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

This trial seeked to extend the preliminary findings of efficacy by evaluating MBG453 in combination with hypomethylating agents (HMA) and also Bcl-2 inhibitor venetoclax.

Study identification

NCT ID
NCT04150029
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
90 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 100 Years
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
Aug 31, 2020
Primary completion
Oct 24, 2024
Completion
Oct 24, 2024
Last update posted
Jan 12, 2026

2020 – 2024

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
25Uni of Alabama at Birmingham Birmingham Alabama 35294
Yale University School Of Medicine New Haven Connecticut 06520
Uni Of Iowa Hospitals And Clinics Iowa City Iowa 52242
Dana Farber Cancer Institute Boston Massachusetts 02215
Mayo Clinic Rochester Rochester Minnesota 55905
Memorial Sloan Kettering New York New York 10017
Weill Cornell Medicine NY-Presb New York New York 10021
Levine Cancer Insitute Carolinas Healthcare System Charlotte North Carolina 28204
Duke Univ Medical Center Durham North Carolina 27710
Chattanooga Onc And Hem Assoc PC Chattanooga Tennessee 37404
MD Anderson Cancer Center University of Texas Houston Texas 77030
Huntsman Cancer Institute Univ of Utah Salt Lake City Utah 84112 0550

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04150029, 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 Jan 12, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04150029 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →