CI

At a glance

ClinicalIndex Comparison Record
N/AActive· 3 enrolled
Drug / intervention
CliniMACSdevice
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/NCT05236764
NCT05236764N/AActive

T-Cell Receptor Alpha Beta+/CD19+ Depletion in Haploidentical Allogeneic Hematopoietic Cell Transplantation (Allo-HCT) for Adult and Pediatric Patients With Hematological Malignancies and Non-malignant Disorders

Baylor College of Medicine·interventional·Posted Feb 11, 2022·Updated Oct 30, 2025

In Brief

A clinical study evaluating CliniMACS for Acute Lymphoblastic Leukemia in Remission and 10 related conditions. Active but no longer recruiting, targeting 3 participants across 2 sites.

Detailed Summary

Patients with medical conditions requiring allogeneic hematopoietic cell transplantation (allo-HCT) are at risk of developing a condition called graft versus host disease (GvHD) which carries a high morbidity and mortality. This is a phase I/II study that will test the safety and efficacy of hematopoietic cell transplantation (HCT) with ex-vivo T cell receptor Alpha/Beta+ and CD19 depletion to treat patients' underlying condition. This process is expected to substantially decrease the risk of GvHD thus allowing for the elimination of immunosuppressive therapy post-transplant. The study will use blood stem/progenitor cells collected from the peripheral blood of parent or other half-matched (haploidentical) family member donor. The procedure will be performed using CliniMACS® TCRα/β-Biotin System which is considered investigational.

Study Details

Timeline

N/AActiveOverdue
20222023202420252026
First PostedFeb 11, 2022
Enrollment StartDec 6, 2023
Primary CompletionAug 29, 2024
Study CompletionMay 23, 2026
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 4.4 years ago

Interventions

CliniMACSdevice

Peripheral blood stem cells from closely matched unrelated donors will be processed using the CliniMACS device to remove TCRalpha/beta (alpha beta+) T cells and B cells, in accordance with the Investigator Brochure and Technical Manual following the laboratory standard operating procedures (SOPs) and using aseptic technique