Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2010-023453-11Phase 3Completed
Phase 3, randomised, double-blind trial in complicated urinary tract infection (cUTI) and pyelonephritis comparing CXA-201 intravenous arm with Levofloxacin intravenous arm (2 arms). Primary endpoint: Microbiological response rate in the microbiologically evaluable population at the test-of-cure visit. Started Apr 2011; 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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