Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03830463Phase 1Completed
Phase 1, randomised, double-blind trial in schizophrenia comparing CTP-692 with Placebo (2 arms). Primary endpoints: Number of Participants with Adverse Events as a Measure of Safety at 48 hours, Measurement of CTP-692 exposure in plasma under fasted conditions at 48 hours and 1 more. Started Jan 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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