Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02071758Phase 1Completed
Phase 1, randomised, open-label trial of LEISH-F3 + GLA-SE in visceral leishmaniasis (VL) (4 arms), sponsored by Access to Advanced Health Institute. Primary endpoint: Number of Adverse Events at 421 days. Started Apr 2014; 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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