Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07694557Phase 1Recruiting
Phase 1, randomised, double-blind trial in respiratory syncytial virus infection (RSV) comparing YKYY025 group with YKYY025 Placebo group (2 arms). Primary endpoints: Adverse Events at 30 days, Serious Adverse Events at 12 months and 4 more. Started Jul 2026; 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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