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Active, not recruiting Phase 2 Interventional

Venetoclax in Combination With ASTX727 for the Treatment of Chronic Myelomonocytic Leukemia and Other Myelodysplastic Syndrome/Myeloproliferative Neoplasm

ClinicalTrials.gov ID: NCT05600894

Public ClinicalTrials.gov record NCT05600894. 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 1, 2026, 2:17 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

Venetoclax In Combination With ASTX727, an All-ORal TherapY for Chronic Myelomonocytic Leukemia and Other MDS/MPN With Excess Blasts (VICTORY-MDS/MPN): a Randomized, Phase 2 Trial

Brief summary

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

This phase II trial tests whether decitabine and cedazuridine (ASTX727) in combination with venetoclax work better than ASTX727 alone at decreasing symptoms of bone marrow cancer in patients with chronic myelomonocytic leukemia (CMML), myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) with excess blasts. Blasts are immature blood cells. Decitabine is in a class of medications called hypomethylation agents. It works by helping the bone marrow produce normal blood cells and by killing abnormal cells in the bone marrow. Cedazuridine is in a class of medications called cytidine deaminase inhibitors. It prevents the breakdown of decitabine, making it more available in the body so that decitabine will have a greater effect. 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. The combination of ASTX727 and venetoclax may be more effective in reducing the cancer signs and symptoms in patients with CMML, or MDS/MPN with excess blasts.

Study identification

NCT ID
NCT05600894
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
132 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years 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
Jun 26, 2023
Primary completion
Aug 30, 2027
Completion
Aug 30, 2027
Last update posted
Aug 18, 2026

2023 – 2027

United States locations

U.S. sites
33
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
Mayo Clinic Hospital in Arizona Phoenix Arizona 85054
UC Irvine Health Cancer Center-Newport Costa Mesa California 92627
UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care Irvine California 92612
UCI Health Laguna Hills Laguna Hills California 92653
Los Angeles General Medical Center Los Angeles California 90033
USC / Norris Comprehensive Cancer Center Los Angeles California 90033
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California 92868
University of California Davis Comprehensive Cancer Center Sacramento California 95817
Yale University New Haven Connecticut 06520
Mayo Clinic in Florida Jacksonville Florida 32224-9980
Northwestern University Chicago Illinois 60611
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
UC Comprehensive Cancer Center at Silver Cross New Lenox Illinois 60451
University of Chicago Medicine-Orland Park Orland Park Illinois 60462
University of Kansas Cancer Center Kansas City Kansas 66160
University of Kansas Hospital-Westwood Cancer Center Westwood Kansas 66205
University of Maryland/Greenebaum Cancer Center Baltimore Maryland 21201
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
NYP/Weill Cornell Medical Center New York New York 10065
Montefiore Medical Center-Einstein Campus The Bronx New York 10461
Montefiore Medical Center-Weiler Hospital The Bronx New York 10461
Montefiore Medical Center - Moses Campus The Bronx New York 10467
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
University of Cincinnati Cancer Center-UC Medical Center Cincinnati Ohio 45219
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210
University of Cincinnati Cancer Center-West Chester West Chester Ohio 45069
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232
Huntsman Cancer Institute/University of Utah Salt Lake City Utah 84112
University of Virginia Cancer Center Charlottesville Virginia 22908
VCU Massey Comprehensive Cancer Center Richmond Virginia 23298

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 NCT05600894, 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 18, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05600894 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →