CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 314 enrolled
Drug / intervention
PBSCs +2 moreother
Likely dose
Not stated in 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/NCT05290545
NCT05290545Phase 3Completed

A Comparative Study of Haploidentical Transplantation Supported by Third-party Cord Blood and Haploidentical Transplantation in Hematological Malignancies

Nanfang Hospital, Southern Medical University·interventional·Posted Mar 22, 2022·Updated Aug 13, 2024

In Brief

A Phase 3 clinical trial evaluating PBSCs, Cord, and 1 other intervention for Hematological Malignancies and Hematopoietic Stem Cell Transplantation. Completed, enrolled 314 participants across 1 site.

Detailed Summary

The objective of this study was to explore whether the combination with umbilical cord blood (UCB) is associated with superior disease-free survival (DFS) in the setting of haploidentical donors (HID) transplantation.

Study Details

Timeline

Phase 3CompletedFinished
2023202420252026
First PostedMar 22, 2022
Enrollment StartFeb 15, 2022
Primary CompletionJan 2, 2023
Study CompletionMar 30, 2024
TodayJul 1, 2026
Enrollment to primary: 11 monthsPosted 4.3 years ago

Interventions

PBSCsother

PBSCs harvest is performed from day 5 of G-CSF to obtain at least 7.0×10\^8 total nucleated cells/kg recipient ideal body weight.

Cordother

The criteria for cord selection included the following: (1) ≥3 of 6 HLA loci , (2) blood type matches, (3) contained a minimum cell count of 0.3×10\^8 nucleated cells/kg and 0.15×10\^6 CD34-positive cells/kg before freezing. The third party UCB will be infused the day after infusion of PBSCs.

BMSCsother

BMSCs of donor will be collected and infused at least 0.5×10\^8 total nucleated cells/kg recipient ideal body weight the day after PBSCs infusion.