Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07903831Phase 1Not yet recruiting
Phase 1, randomised, double-blind trial in hepatitis B (HBV) comparing SCTA02A with Placebo (2 arms). Primary endpoints: Treatment-Related Adverse Events at 16 weeks, Maximum Tolerated Dose at 16 weeks and 1 more. Planned start Oct 2026; status: not yet 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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