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Trials / Completed

CompletedNCT04965337

Study to Evaluate Safety, Tolerability and Pharmacokinetics of ASC42 in Chinese Healthy Subjects

A Phase I Randomized, Double-Blind, Placebo-Controlled, Dose Escalation, Single Center Bridging Study to Evaluate Safety, Tolerability and Pharmacokinetics of ASC42 in Chinese Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Ascletis Pharmaceuticals Co., Ltd. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a Phase I Randomized, Double-Blind, Placebo-Controlled, Dose Escalation, Single Center Bridging Study to Evaluate Safety, Tolerability and Pharmacokinetics of ASC42 in Chinese Healthy Subjects.

Conditions

Interventions

TypeNameDescription
DRUGASC42ASC42 tablet administered orally
DRUGPlaceboMatching placebo administered orally

Timeline

Start date
2021-07-11
Primary completion
2021-08-01
Completion
2021-08-01
First posted
2021-07-16
Last updated
2022-06-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04965337. Inclusion in this directory is not an endorsement.

Study to Evaluate Safety, Tolerability and Pharmacokinetics of ASC42 in Chinese Healthy Subjects (NCT04965337) · Clinical Trials Directory