Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03636204Phase 1Completed
Phase 1, randomised, double-blind trial in frontotemporal dementia (FTD) comparing AL001 with Placebo (2 arms). Primary endpoints: Number of subjects with adverse events at 85 days and Number of subjects with Dose Limiting Adverse Event (DLAEs) at 85 days. Started Sep 2018; 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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