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RECRUITING
NCT03214354
PHASE2

Nonmyeloablative Stem Cell Transplant in Children with Sickle Cell Disease and a Major ABO-Incompatible Matched Sibling Donor

Sponsor: University of Calgary

View on ClinicalTrials.gov

Summary

The aim of this study to evaluate the safety and efficacy of a nonmyeloablative conditioning regimen for allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients with sickle cell disease (SCD) who have a matched related major ABO-incompatible donor. The nonmyeloablative regimen will use alemtuzumab, total body irradiation (TBI) and sirolimus for immune suppression. This study will expand the access of HSCT for patients with SCD who are currently not eligible because of donor restrictions.

Official title: A Phase II Pilot Study of Nonmyeloablative Conditioning Hematopoietic Stem Cell Transplantation in Children with Sickle Cell Disease Who Have a Matched Related Major ABO-Incompatible Donor (Sickle-AID)

Key Details

Gender

All

Age Range

1 Year - 19 Years

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2017-07-05

Completion Date

2028-07

Last Updated

2024-12-10

Healthy Volunteers

No

Interventions

DRUG

Alemtuzumab

Alemtuzumab, Day -7 to -3. Dose: 0.2mg/kg/dose SC once daily x 5 days

RADIATION

Total Body Irradiation

TBI 300 cGy on Day -2

DRUG

Sirolimus

Sirolimus is used for GVHD prophylaxis

Locations (1)

Alberta Children's Hospital

Calgary, Alberta, Canada