Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02819271Phase 1Completed
Phase 1, randomised, double-blind trial in heart failure (HF) comparing BMS-986231 with Placebo (2 arms). Primary endpoints: Treatment Emergent Adverse Events at 31 days and Tolerability measured by percentage of Treatment Emergent Adverse Events at 31 days. Started Feb 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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