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A Study of Participants with Β-Thalassemia Treated with Betibeglogene Autotemcel
Sponsor: Genetix Biotherapeutics Inc.
Summary
The main aim of this study is to collect real-world longitudinal data on participants with β-thalassemia treated with betibeglogene autotemcel (beti-cel) in the post marketing setting. To assess the long-term safety, including the risk of newly diagnosed malignancies, after treatment with beti-cel and evaluate the long-term effectiveness of treatment with beti-cel.
Official title: A Safety and Effectiveness Registry Study of Patients with Β-Thalassemia Treated with Betibeglogene Autotemcel (the Glostar Registry)
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
150
Start Date
2024-01-23
Completion Date
2043-12
Last Updated
2025-02-11
Healthy Volunteers
No
Conditions
Interventions
No Intervention
This is non-interventional study.
Locations (6)
UCSF Benioff Children's Hospitals
Oakland, California, United States
Stanford University
Palo Alto, California, United States
University of Minnesota
Minneapolis, Minnesota, United States
Cohen Children's Medical Center
New Hyde Park, New York, United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Texas Children's Hospital
Houston, Texas, United States