RecruitingPhase 2NCT07084012
A Phase IIa Clinical Trial to Evaluate the Efficacy and Safety of Intravenous Infusion of hUC-MSCs in Patients With AIS
Studying Androgen insensitivity syndrome
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 Wingor Biotechnology Co., Ltd.
- Intervention
- hUC-MSCs treatment (high dose)(drug)
- Enrollment
- 60 target
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2025 – 2026
Study locations (1)
- Beijing Tiantan Hospital, Capital Medical University, Beijing, Beijing Municipality, China
Collaborators
Beijing Tiantan Hospital
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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