Gene Correction in Autologous CD34+ Hematopoietic Stem Cells (HbS to HbA) to Treat Severe Sickle Cell Disease
Start Date
11/15/2021
Completion Date
12/31/2028
Summary
This study is a first-in-human, single-arm, open-label Phase I/II study of nula-cel in approximately 15 participants, diagnosed with severe Sickle Cell Disease. The primary objective is to evaluate safety of the treatment in this patient population, as well as preliminary efficacy and pharmacodynamic data.
Detailed Description
Participants diagnosed with severe SCD will receive nula-cel via IV infusion following myeloablative conditioning in an autologous HSCT setting.
Eligibility Criteria
Age Range: 12 years to 50 years
Interventions
nula-cel Drug Product
Conditions
Locations
Children's Hospital Los Angeles
Los Angeles, California 90027
United States
Lucile Packard Children's Hospital
Palo Alto, California 94304
United States
Washington University
St Louis, Missouri 63110
United States
Columbia University Irving Medical Center
New York, New York 10032
United States
Memorial Sloan Kettering
New York, New York 10065
United States
Nationwide Children's Hospital
Columbus, Ohio 43205
United States