RecruitingNot applicableNCT06041620
Safety and Efficacy Evaluation of Autologous CRISPR-Cas12b Edited Hematopoietic Stem Cells
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
- Institute of Hematology & Blood Diseases Hospital, China
- Principal Investigator
- Jun Shi, PhDInstitute of Hematology & Blood Diseases Hospital, China
- Intervention
- VGB-Ex01(biological)
- Enrollment
- 2 enrolled
- Eligibility
- 3-35 years · All sexes
- Timeline
- 2023 – 2026
Study locations (1)
- Regenerative Medicine Center, Tianjin, Tianjin Municipality, China
Collaborators
Shanghai Vitalgen BioPharma Co., Ltd.
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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