Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06595706Phase 1Completed
Phase 1, randomised, double-blind trial in multiple sclerosis (MS) comparing Lucid-21-302 with Placebo (2 arms). Primary endpoints: Incidence, severity and relationship of Adverse Events (AEs) up to 15 days, Incidence of Serious AEs (SAEs) and suspected unexpected SAEs up to 15 days and 16 more. Started Sep 2024; 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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