Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07760467Phase 1Recruiting
Phase 1, randomised, double-blind trial in paroxysmal nocturnal hemoglobinuria (PNH) comparing TUL321 with Placebo (2 arms). Primary endpoints: Incidence of adverse events up to 17 days and Changes from baseline in physical examinations, vital signs, electrocardiograms (ECG), and laboratory tests up to 17 days. Started Aug 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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