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Clinical Trial Summary

A single ascending oral dose(s) study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of YCT-529 in healthy male subjects.


Clinical Trial Description

This is a Phase 1a, double-blind, placebo controlled, first in human study to evaluate the safety, tolerability, PK, and PD of YCT-529 in 2 cohorts of 8 subjects. Cohorts 1 and 2 will be dosed in the fasted state in Periods 1 and 2. Each cohort will receive two doses of study drug separated by a washout period. One cohort will then return for a third dose of study drug under fed conditions in Period 3 to study the effect of food on YCT-529. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06094283
Study type Interventional
Source YourChoice Therapeutics, Inc.
Contact Nadja Mannowetz, PhD
Phone 415 233-6970
Email ClinicalTrial@ychoicetx.com
Status Recruiting
Phase Phase 1
Start date December 20, 2023
Completion date June 2024

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