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A Study to Evaluate the Safety, Tolerability, PK and PD of AP303 in Healthy Chinese Participants

Healthy Subjects Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled Multiple-ascending Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AP303 Following 2-week Oral Administration in Healthy Chinese Participants.

Clinical Trial Summary

The study will be a single center, double-blind, randomized, placebo-controlled, multiple-ascending-dose study to evaluate the safety, tolerability, PK and PD of AP303 following 2-week oral administration to healthy Chinese participants.

Clinical Trial Description

Eligible study participants will be enrolled and randomized into one of the two dose cohorts, each cohort will include 9 participants randomized to AP303 and placebo at 2:1 ratio (6 on AP303 and 3 on placebo). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06308523
Study type Interventional
Source Alebund Pharmaceuticals
Contact
Status Completed
Phase Phase 1
Start date March 18, 2024
Completion date May 13, 2024
View Details
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