Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04961658Phase 1Terminated
Phase 1, open-label trial of GEM 00220 in septic shock (5 arms), sponsored by Northern Therapeutics. Primary endpoints: Incidence of Adverse Events at 28 days and Maximum Feasible Tolerated Dose at 28 days. Started Aug 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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