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

  • STATUS
    Recruiting
  • participants needed
    300
  • sponsor
    Bellus Health Inc
Updated on 16 September 2021
Investigator
Kristin Bartholomew
Primary Contact
Clinical Research of Rock Hill (3.3 mi away) Contact
+134 other location

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).

Description

The primary objective of this study is to determine the therapeutic dose of BLU-5937 in patients with refractory chronic cough by assessing the change from baseline to week 4 in the 24-hour cough frequency with BLU-5937 relative to placebo.

Details
Condition Refractory Chronic Cough
Treatment Placebo, BLU-5937
Clinical Study IdentifierNCT04678206
SponsorBellus Health Inc
Last Modified on16 September 2021

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