drugset / Trial / NCT03282591

Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Refractory Chronic Cough

NCT03282591 ↗

Phase 2 Completed 185 enrolled Vyne Therapeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Study of the efficacy, safety, and tolerability of serlopitant for the treatment of refractory chronic cough

Timeline

Start
2017-10-03
Primary completion
2018-08-15
Completion
2018-09-06

Outcome

Missed primary endpoint

registry analysis (superiority test); Serlopitant 5 mg vs Placebo; p = 0.9942; Mean Difference (Final Values) 31.4; Mixed Models Analysis NCT03282591 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Serlopitant Small molecule 5 mg —