RecruitingPhase 1NCT07422298
A Study to Evaluate the Effect of BMS-986278 on Cardiac Repolarization in Healthy Participants
A Phase 1, Randomized, Double-blind, Positive-controlled, Placebo-controlled, 4-Period Crossover, Thorough QT/QTc Study to Evaluate the Effect of Multiple Doses of BMS-986278 on Cardiac Repolarization in Healthy Participants
Sponsor
Bristol-Myers Squibb
Enrollment
32 participants
Start Date
Feb 19, 2026
Study Type
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to evaluate the effect of BMS-986278 on the cardiac repolarization in healthy participants.
Eligibility
Min Age: 18 YearsMax Age: 55 Years
Inclusion Criteria3
- Female individuals not of childbearing potential and males.
- Healthy as determined by medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory assessments.
- to 55 years of age, inclusive, at the time of signing the informed consent with a BMI 18.0 to 32.0 kg/m2, inclusive.
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Interventions
DRUGBMS-986278
Specified dose on specified days
DRUGPlacebo
Specified dose on specified days
DRUGMoxifloxacin
Specified dose on specified days
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07422298
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