CompletedEarly Phase 1NCT06024265
The Safety and Tolerability Study With ER2001 Intravenous Injection 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
- Xia Meng, Ph.DExoRNA Bioscience
- Intervention
- ER2001 injection(drug)
- Enrollment
- 10 enrolled
- Eligibility
- 25-55 years · All sexes
- Timeline
- 2023 – 2025
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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