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Trials / Enrolling By Invitation

Enrolling By InvitationNCT07098091

Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics of YD0293 in Healthy Subjects

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Food Effect of Single and Multiple Doses of YD0293 Tablets in Healthy Subjects

Status
Enrolling By Invitation
Phase
Phase 1
Study type
Interventional
Enrollment
78 (estimated)
Sponsor
Shanghai Yidian Pharmaceutical Technology Development Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study is a single-center, single- and multiple-dose escalating study with a food-effect component, designed to evaluate the safety, tolerability, and pharmacokinetic (PK) characteristics of YD0293 tablets following a single oral dose in healthy subjects, as well as the effect of food on PK parameters and the potential effect on the QT interval. The study also aims to assess the safety, tolerability, and PK profile of YD0293 tablets following multiple oral doses in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGYD0293YD0293 tablet for oral administration
DRUGYD0293 placeboYD0293 placebo tablet for oral administration

Timeline

Start date
2025-02-26
Primary completion
2025-12-31
Completion
2025-12-31
First posted
2025-08-01
Last updated
2025-08-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07098091. Inclusion in this directory is not an endorsement.