Clinical Trials Directory

Trials / Completed

CompletedNCT05195203

A Study of HS-10353 in Chinese Participants.

A Phase I Randomized, Double-blinded, Placebo-controlled Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetic of HS-10353 in Chinese Adult Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
96 (actual)
Sponsor
Jiangsu Hansoh Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The primary objective of this study is to assess the safety and tolerability of single and multiple oral administered doses of HS-10353 separately in Chinese healthy and major depressive disorder subjects.

Detailed description

This is a phase I, randomized, double-blinded, placebo-controlled, both single ascending doses (SAD) study and multiple ascending dose (MAD) clinical trial to assess the safety, tolerability, and pharmacokinetics of HS-10353 tablet(s) separately in Chinese healthy and major depressive disorder (MDD) subjects. Approximately six sequential dose cohorts will be evaluated in SAD study. Sentinel dosing will be employed for the first SAD cohort to protect the subjects' safety. Escalation to the next dose cohort will be undertaken only after safety and PK data are reviewed by the Safety Review Committee (SRC) and agreement reach that it is safe to increase the dose. Each SAD cohort is dosed at approximately weekly intervals to allow adequate time for collection and review of safety and PK data. Approximately three sequential dose cohorts will be evaluated in MAD study. The total daily dose for each MAD cohort will be based on information obtained from the SAD study. Each subject will receive only one dose regimen in this study. Safety data up to Day14 (±1) in SAD and up to Day20 (±1) in MAD will be reviewed prior to the next dose level. The number of Cohorts in SAD and MAD would be adjusted based on the assessment of SRC.

Conditions

Interventions

TypeNameDescription
DRUGHS-10353Single or multiple dose(s) of HS-10353
DRUGPlaceboSingle or multiple dose(s) of placebo

Timeline

Start date
2021-01-27
Primary completion
2023-03-11
Completion
2023-03-31
First posted
2022-01-18
Last updated
2023-08-03

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05195203. Inclusion in this directory is not an endorsement.