CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 250 target
Drug / intervention
Cytarabine +1 moredrug
Likely dose
Cytarabine 3gfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03031262
NCT03031262Phase 2ActiveUpdate OverdueUpdated 13mo ago · Completion was 14mo ago
Enrollment Stalled

Efficacy and Safety of Chidamide in CBF Leukemia

Institute of Hematology & Blood Diseases Hospital, China·interventional·Posted Jan 25, 2017·Updated May 30, 2025

In Brief

A Phase 2 clinical trial evaluating Cytarabine and Chidamide for AML. Active but no longer recruiting, targeting 250 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

In this open-label, randomized, prospective clinical trial, CBF acute myeloid leukemia (AML) patients who have reached CR are randomised into two groups and receive high-dose cytarabine (HDAC) or high-dose cytarabine plus chidamide.The safety and efficacy of chidamide is evaluated.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAML
CountriesChina
Collaborators--

Timeline

Phase 2Active
201720182019202020212022202320242025202620272028
First PostedJan 25, 2017
Enrollment StartFeb 8, 2017
Primary CompletionApr 10, 2025
Study CompletionDec 30, 2027
TodayJul 1, 2026
Enrollment to primary: 8.2 yearsPosted 9.4 years ago

Interventions

Cytarabinedrug

Cytarabine at a dose of 3g/㎡/d on the first, third and fifth day.

Chidamidedrug

Chidamide at a dose of 20mg/d twice a week for 3 months.