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Trials / Completed

CompletedNCT06476821

A Study to Evaluate the Safety, Tolerability, Drug Levels, and Drug Effects of Single Doses of BMS-986435 (MYK-224) in Healthy Chinese Participants

A Phase 1 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Doses of BMS-986435 (MYK-224) in Healthy Chinese Participants

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Bristol-Myers Squibb · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics following a single oral dose of BMS-986435 in healthy adult Chinese participants.

Conditions

Interventions

TypeNameDescription
DRUGBMS-986435Specified dose on specified days

Timeline

Start date
2024-06-27
Primary completion
2024-10-11
Completion
2024-10-11
First posted
2024-06-26
Last updated
2024-11-19

Locations

1 site across 1 country: China

Regulatory

Source: ClinicalTrials.gov record NCT06476821. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Safety, Tolerability, Drug Levels, and Drug Effects of Single Doses of BMS-986435 (MYK-224) in H (NCT06476821) · Clinical Trials Directory