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A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Pharmacodynamic Profiles and Food Effect of CS32582 Capsules

Healthy Clinical Trial

Official title:
A Phase 1, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Pharmacodynamic Profiles Following Single and Multiple Doses and Food Effect of CS32582 Capsules in Healthy Adult Subjects

Clinical Trial Summary

The study is to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic profiles of CS32582 after single or multiple oral administration, as well as the food effect on the pharmacokinetics in healthy subjects.

Clinical Trial Description

This study consists of 3 parts: single ascending dose (SAD), food effect (FE) and multiple ascending dose (MAD). Both SAD and MAD study are randomized, double-blind, placebo-controlled design. The FE study is a randomized, open-label, two-period, two-crossover design. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06224595
Study type Interventional
Source Chipscreen Biosciences, Ltd.
Contact Hongrong Xu, Ph.D
Phone 86-21-31587858
Email xu.hongrong@zs-hospital.sh.cn
Status Not yet recruiting
Phase Phase 1
Start date March 16, 2024
Completion date June 22, 2025
View Details
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