CompletedPhase 1NCT06216054
Safety, Tolerability and Pharmacokinetic of Multiple-ascending Doses of LPM3770164 in Healthy Subjects
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
- Luye Pharma Group Ltd.
- Principal Investigator
- Huafang Li, DoctorShanghai Mental Health Center
- Intervention
- LPM3770164 sustained release tablet(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2023 – 2024
Study locations (1)
- Shanghai Mental Health Center, Shanghai, Shanghai Municipality, 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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