Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00121862Phase 2Completed
Phase 2, randomised, double-blind trial of Leish-111f + MPL-SE in cutaneous leishmaniasis (CL) (3 arms), sponsored by Access to Advanced Health Institute. Primary endpoints: Adverse events, Dose-limiting toxicities at Day 84 and 1 more. Started Aug 2005; 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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