Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04008992Phase 1Completed
Phase 1, randomised, double-blind trial of FA relaxin in heart failure (HF) (13 cohorts), sponsored by Bristol Myers Squibb. Primary endpoints: Incidence of Adverse Events (AEs) up to 7 weeks, Incidence of Serious Adverse Events (SAEs) up to 7 weeks and 5 more. Started Jun 2019; 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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