Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05413668Phase 1Completed
Phase 1, randomised, double-blind trial comparing RVP-001 with Placebo (2 arms). Primary endpoints: Safety and tolerability of single ascending doses, Pharmacokinetic (PK) Parameter Cmax at 120 hours and 4 more. Started May 2022; 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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