Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03884491Phase 1Completed
Phase 1, open-label, single-arm trial of vortioxetine in major depressive disorder (MDD), sponsored by Lundbeck. Primary endpoints: Absolute Bioavailability (F) at 72 hours and Time to Maximum Plasma Concentration (tmax) at 72 hours. Started Mar 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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