CompletedPhase 1NCT05238701

A Dose-escalation Study to Evaluate the Safety, Tolerability and Pharmacokinetic of LPM3770164 in Healthy Subjects

Studying Huntington disease

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Luye Pharma Group Ltd.
Principal Investigator
hufang Li, Doctor
Shanghai Mental Health Center
Intervention
LPM3770164 sustained release tablet(drug)
Enrollment
104 enrolled
Eligibility
18-45 years · All sexes
Timeline
20222023

Study locations (1)

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.

Open NCT05238701 on ClinicalTrials.gov

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