Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04972227Phase 1Completed
Phase 1, randomised, double-blind trial in schizophrenia comparing CY6463 with Placebo (2 arms). Primary endpoint: Number of participants with treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), and TEAEs leading to study drug discontinuation at 28 days. Started Sep 2021; 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.
See how Gosset can support your research on NCT04972227.