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NOT YET RECRUITING
NCT07867626
PHASE2

Phase II De-Escalation Study of Metronomic Decitabine/Cedazuridine Plus Venetoclax in AML

Sponsor: Rutgers, The State University of New Jersey

View on ClinicalTrials.gov

Summary

To evaluate the 12-month relapse free survival with weekly Decitabine/cedazuridine plus Venetoclax in AML maintenance after achieving composite CR (CR, CRi, CRh)

Official title: A Phase II De-Escalation Study of Metronomic Decitabine/Cedazuridine Plus Venetoclax in Acute Myeloid Leukemia Maintenance.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

41

Start Date

2026-09-30

Completion Date

2029-12

Last Updated

2026-10-09

Healthy Volunteers

No

Interventions

DRUG

Venetoclax, Decitabine/Cedaruridine

Patients who consent to the study will receive weekly Decitabine/Cedaruridine plus Venetoclax until intolerance or disease progression. Both Decitabine/Cedaruridine and Venetoclax are administered orally once on D1, 8, 15, 22 each

DRUG

decitabine/cedazuridine

Patients who consent to the study will receive weekly decitabine/cedazuridine plus Venetoclax until intolerance or disease progression. Venetoclax is administered orally once on D1, 8, 15, 22 each 28-day cycle with food and water. Decitabine/Cedazuridine is administered orally once on D1, D8, D15 D22 with empty stomach.

Locations (1)

Rutgers Cancer Institute

New Brunswick, New Jersey, United States