RecruitingEarly Phase 1NCT05864170
the Safety and Efficacy Evaluation of HGI-001 Injection in Patients With Transfusion-Dependent β-Thalassemia
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(biological)
- Enrollment
- 3 target
- Eligibility
- 18-35 years · All sexes
- Timeline
- 2022 – 2025
Study locations (1)
- Shenzhen University General Hospital, Shenzhen, Guangdong, 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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