Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02753855Phase 1Completed
Phase 1, open-label, single-arm trial of telavancin in bacterial infection, sponsored by University of Illinois Chicago. Primary endpoints: Number (%) of adverse events of any severity regardless of relationship to study drug at 48 hours, Area-under-the-plasma concentration-time curve (AUC0-infinity) at 48 hours and 1 more. Started Apr 2016; 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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