Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2010-021424-94Phase 3Completed
Phase 3, randomised, double-blind trial in acute bacterial skin and skin structure infection (ABSSSI) and bacterial wound infection comparing Single-dose oritavancin with Vancomycin for 7 to 10 days (2 arms). Primary endpoint: Early clinical response at 48 to 72 hours. Started Dec 2010; 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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