RecruitingPhase 2NCT05198323
A Study to Evaluate the Safety and Efficacy of LT3001 Drug Product in Subjects AIS Undergoing EVT
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
- Lumosa Therapeutics Co., Ltd.
- Intervention
- LT3001 Drug Product(drug)
- Enrollment
- 66 target
- Eligibility
- 18-90 years · All sexes
- Timeline
- 2022 – 2026
Study locations (2)
- CHI Memorial Hospital, Chattanooga, Tennessee, United States
- Taichung Medical University, Taichung, Taiwan
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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