About this trial
Observe long-term safety risk and long-term efficacy after intravenous infusion of BRL-101 in TDT subjects.
Eligibility criteria
Qualifiers
Provision of written informed consent for this study by subjects, or as applicable, subject's parent(s)/legal guardian(s)
Treated with BRL-101 for therapy of transfusion-dependent β-thalassemia.
Disqualifiers
None
Trial design
Treatments tested in this trial
- Assessments
Treatment groups
Sponsors and collaborators
Bioray Laboratories
Lead sponsor
First Affiliated Hospital of Guangxi Medical University
Collaborator
Xiangya Hospital of Central South University
Collaborator
Chinese Academy of Medical Sciences
Collaborator
Nanfang Hospital, Southern Medical University
Collaborator
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Collaborator
The 923rd Hospital of Joint Logistics Support Force of People's Liberation Army
Collaborator
Shenzhen Children 's Hospital
Collaborator