CI

At a glance

ClinicalIndex Comparison Record
Phase 3Unknown· 100 target
Drug / intervention
HMA+DLI +1 morecombination
Likely dose
HMA+DLI 20mg/m2from 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/NCT03662087
NCT03662087Phase 3Unknown

Hypomethylating Agents + Donor Lymphocyte Infusion vs Donor Lymphocyte Infusion Preemptive Therapy Based on Minimal Residual Disease for Acute Leukemia Undergoing Allogenetic Hematopoietic Stem Cell Transplantation

Nanfang Hospital, Southern Medical University·interventional·Posted Sep 7, 2018·Updated Sep 7, 2018

In Brief

A Phase 3 clinical trial evaluating HMA+DLI and DLI for Minimal Residual Disease,Acute Leukemia, Hypomethylating Agents, Donor Lymphocyte Infusion, Allogeneic Hematopoietic Cell Transplantation. Targeting 100 participants across 1 site.

Detailed Summary

Allogeneic hematopoietic cell transplantation (Allo-HSCT) is an effective therapy for acute leukemia, but relapse is the most common problem affecting long-term survivors of allo-HSCT. Therapy options for relapse include stopping immune suppression, re-induction of chemotherapy, donor lymphocyte infusion (DLI) or combination therapy. In this prospective randomized controlled study, the safety and efficacy of hypomethylating agents (HMA) + DLI and DLI preemptive therapy based on minimal residual disease in acute leukemia undergoing allo-HSCT are evaluated.

Study Details

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

Timeline

Phase 3UnknownOverdue
20192020202120222023202420252026
First PostedSep 7, 2018
Enrollment StartOct 1, 2018
Primary CompletionOct 1, 2021
Study CompletionOct 1, 2022
TodayJul 1, 2026
Enrollment to primary: 3 yearsPosted 7.8 years ago

Interventions

HMA+DLIcombination

HMA: Decitabine was administered at 20mg/m2/day for five consecutive days or Ara-C was administered at 75mg/m2/day for seven consecutive days. DLI was administered at a median dose of 1.0 (range 0.7-1.4) ×10\*8 mononuclear cells/kg.

DLIbiological

DLI was administered at a median dose of 1.0 (range 0.7-1.4) ×10\*8 mononuclear cells/kg.