Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05829629Phase 1Recruiting
Phase 1, randomised, double-blind trial in human papillomavirus infection, cervical intraepithelial neoplasia (CIN) and Squamous Intraepithelial Lesion (SIL) comparing FluBHPVE6E7 with Placebo (2 arms). Primary endpoint: Frequency and severity of adverse events at 7 days. Started Sep 2023; status: recruiting.
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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