Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07347678Phase 1Recruiting
Phase 1, randomised trial in hypercholesterolemia comparing RN5681 with Placebo (2 arms). Primary endpoints: Safety and tolerability of subcutaneously administered RN5681 at Day 180 and Metabolic markers of efficacy at Day 180. Started Mar 2026; status: 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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