RecruitingPhase 1NCT06655662
Evaluating Safety and Efficacy of Lentiviral-transduced CD34+ HSCs in Β-thalassaemia Patients.
Studying Thalassemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Shenzhen Hemogen
- Principal Investigator
- Chao Liu, PHDShenzhen Hemogen
- Intervention
- β-globin restored autologous hematopoietic stem cells(other)
- Enrollment
- 8 target
- Eligibility
- 6-35 years · All sexes
- Timeline
- 2024 – 2026
Study locations (3)
- Guangxi Medical University First Affiliated Hospital, Guangxi, China
- Shenzhen Children's Hospital, Shenzhen, China
- Shenzhen University General Hospital, Shenzhen, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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