Active, not recruitingEarly Phase 1NCT07344519
The Safety and Tolerability Study With ER2001 Intravenous Injection Repetitive Treatment in Adults With Early Manifest Huntington's Disease.
Studying Huntington disease
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
- ExoRNA Bioscience
- Principal Investigator
- pingyi xu, Ph.DFirst Affiliated Hospital of Guangzhou Medical University
- Intervention
- ER2001 injection(drug)
- Enrollment
- 9 enrolled
- Eligibility
- 25 years · All sexes
- Timeline
- 2024 – 2026
Study locations (1)
- First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 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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