Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04076293Phase 1Completed
Phase 1, randomised, double-blind trial in short bowel syndrome (SBS) comparing HM15912 with Placebo (2 arms). Primary endpoints: Number of Participants With Treatment-emergent Adverse Events of HM15912 at 44 days and Number of Participants With Significant Findings Observed for Hematology at 44 days. Started Oct 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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