Jeonbuk National University Hospital | Clinical Pharmacology Center
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This is a randomized, double-blind, placebo-controlled, parallel-arm, Phase 3 study of BLU-5937 in participants with Refractory Chronic Cough (RCC).
Full description
The primary efficacy objective is to assess the effect of BLU-5937 on 24-hour cough frequency in adults with refractory chronic cough (including unexplained chronic cough) at 24 weeks.
Enrollment
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Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
825 participants in 3 patient groups, including a placebo group
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Central trial contact
EU GSK Clinical Trials Call Center; US GSK Clinical Trials call Center
Data sourced from clinicaltrials.gov
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