Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06741072Phase 1Recruiting
Phase 1, randomised, double-blind trial in Epstein-Barr virus infection comparing Group I (OSU-2131, QS-21) with Group II (placebo) (2 arms). Primary endpoints: Incidence of treatment-emergent adverse events at 28 weeks, Changes in laboratory parameters and vital signs at 56 weeks and 2 more. Started Jun 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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