drugset / Trial / NCT04678206
Evaluation of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Camlipixant | Small molecule | 12.5 mg | Oral |
| Subject | Camlipixant | Small molecule | 50 mg | Oral |
| Subject | Camlipixant | Small molecule | 200 mg | Oral |