Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04820049Phase 1Completed
Phase 1, randomised, double-blind trial in acute-on-chronic liver failure (ACLF) comparing F573 Group with Placebo Group (2 arms). Primary endpoints: Maximum Tolerated Dose up to 7 days, Maximum Plasma Concentration up to 7 days and 3 more. Started Feb 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.
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