Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04766476Phase 1Terminated
Phase 1, randomised, double-blind trial of BMS-963272 in non-alcoholic fatty liver disease (NAFLD) (3 arms), sponsored by Bristol Myers Squibb. Primary endpoints: Incidence of adverse events up to 166 days, Incidence of serious adverse events up to 166 days and 4 more. Started Feb 2021; status: terminated.
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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