drugset / Trial / NCT04193202

Efficacy and Safety of Gefapixant (MK-7264) in Adult Participants With Recent Onset Chronic Cough (MK-7264-043)

NCT04193202

Phase 3 Completed 419 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of gefapixant in participants with recent onset chronic cough (duration \>8 weeks after onset of cough symptoms) for \<12 months and a diagnosis of refractory or unexplained chronic cough. The primary hypothesis is that gefapixant is superior to placebo in improving cough-related quality of life measured as change from baseline in the Leicester Cough Questionnaire (LCQ) total score at Week 12.

Timeline

Start
2020-05-21
Primary completion
2021-10-19
Completion
2021-11-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Gefapixant Small molecule 45 mg Oral

Indications

No indication recorded.