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Clinical Trial Summary

A Phase 1, Single-Center, Randomized, Double-Blind, Placebo-Controlled, Single And Multiple Ascending Dose, First-Time-In-Human Study to Assess The Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ECC0509 in Healthy Volunteers.


Clinical Trial Description

This study will be conducted in up to seven cohorts of Single Ascending Dose (SAD) & 3 cohorts of Multiple Ascending Dose (MAD). SAD will consist of a staggered dosing approach with a dose range from 1mg to 80mg. Staggered dosing approach will not be deployed for MAD cohorts with a dose range of 8mg to 40mg. In the MAD cohort, the effect of food will also be assessed by comparing the PK profile of Day 10 fed conditions against Day 14 fasted conditions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05012423
Study type Interventional
Source Eccogene (Shanghai) Co. Ltd
Contact Participant Engagement Manager
Phone 1800150433
Email cmax@cmax.com.au
Status Recruiting
Phase Phase 1
Start date July 7, 2021
Completion date February 20, 2022

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