Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06213363Phase 2Not yet recruiting
Phase 2, randomised, double-blind trial of TCR-1672 in refractory chronic cough (RCC) (3 cohorts), sponsored by Beijing Tide Pharmaceutical Co., Ltd. Primary endpoints: Efficacy Endpoint (24-hour Cough Frequency) at 1 week and Safety Endpoints at 4 weeks. Planned start Feb 2024; status: not yet recruiting.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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