drugset / Trial / NCT03069352

A Study of Venetoclax in Combination With Low Dose Cytarabine Versus Low Dose Cytarabine Alone in Treatment Naive Patients With Acute Myeloid Leukemia Who Are Ineligible for Intensive Chemotherapy

NCT03069352 ↗

Phase 3 Completed 211 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate if venetoclax when co administered with low-dose cytarabine (LDAC) improves overall survival (OS) versus LDAC and placebo, in treatment-naïve patients with acute myeloid leukemia (AML).

Timeline

Start
2017-05-23
Primary completion
2019-02-15
Completion
2025-08-21

Outcome

Missed primary endpoint

registry Placebo + Low Dose Cytarabine (LDAC) vs Venetoclax + Low Dose Cytarabine (LDAC); p = 0.114 NCT03069352 ↗

paper At the primary analysis, the study did not meet its primary endpoint of a statistically significant improvement in overall survival (OS), however, PMID 34599139 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Venetoclax Small molecule 600 mg Oral
Background Cytarabine Small molecule 20 mg/m2 Subcutaneous