Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02157506Phase 2Completed
Phase 2, randomised, double-blind trial of cimlanod, sponsored by Bristol Myers Squibb. Primary endpoints: Number of Participants With Treatment-Emergent Adverse Events at 30 days, Mean Time Averaged Change From Baseline in Adjudicated Pulmonary Capillary Wedge Pressure at 6 hours and 2 more. Started Jun 2014; status: completed.
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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