drugset / Trial / NCT02612610

A 12-Week Study in Participants With Refractory Chronic Cough (MK-7264-012)

NCT02612610

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is designed to evaluate the efficacy of three dose regimens of gefapixant (\[MK-7264\] 7.5 mg, 20 mg, and 50 mg) relative to placebo in reducing awake objective cough frequency. The primary hypothesis for this trial is that at least one dose regimen of gefapixant is superior to placebo with respect to the mean change from baseline in awake cough frequency (on the log scale).

Timeline

Start
2015-12-15
Primary completion
2016-10-31
Completion
2016-11-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Gefapixant Small molecule 7.5 mg Oral
Subject Gefapixant Small molecule 20 mg Oral
Subject Gefapixant Small molecule 50 mg Oral