drugset / Trial / NCT04678206

Evaluation of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough

NCT04678206 ↗

Phase 2 Completed 310 enrolled Bellus Health Inc. - a GSK company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, parallel-arm, Phase 2b adaptive dose-finding study of BLU-5937 in participants with Refractory Chronic Cough (RCC).

Timeline

Start
2020-12-07
Primary completion
2021-10-21
Completion
2021-11-02

Outcome

Met primary endpoint

paper A statistically significant reduction in placebo-adjusted 24-hour cough frequency was seen in the 50 mg (-34.4%; 95% confidence interval, -50.5 to -13.3; P = 0.0033) PMID 40043302 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Camlipixant Small molecule 12.5 mg Oral
Subject Camlipixant Small molecule 50 mg Oral
Subject Camlipixant Small molecule 200 mg Oral