Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05965414Phase 1Completed
Phase 1, randomised, double-blind trial in Alzheimer's disease (AD) comparing CS6253 with Placebo (2 arms). Primary endpoints: Safety and tolerability of CS6253 at Day 13, Plasma Area Under the Curve from time zero to last quantifiable concentration at 72 hours and 8 more. Started Oct 2023; 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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