Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06688058Phase 1Active, not recruiting
Phase 1, randomised, double-blind trial of V540D in human papillomavirus infection (2 arms), sponsored by Merck & Co. Primary endpoints: Number of Participants Who Experience a Solicited Injection-Site Adverse Event (AE) at 26 weeks, Number of Participants Who Experience a Solicited Systemic AE at 26 weeks and 5 more. Started Dec 2024; status: active, not 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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