Stopped: The data did not support study endpoints for acute cough, based on an interim efficacy analysis; not due to safety concerns.
The purpose of the study is to evaluate the efficacy, safety, and tolerability of gefapixant (MK-7264) in adult participants with induced viral upper respiratory tract infections (URTI).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Awake Coughs Per Hour on Day 3
Timeframe: Day 3