Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05828472Phase 1Completed
Phase 1, randomised, double-blind trial of MY-008 in paroxysmal nocturnal hemoglobinuria (PNH) (4 arms), sponsored by Wuhan Createrna Science and Technology Co., Ltd. Primary endpoint: Incidence and severity of adverse events up to 31 days. Started Jan 2023; status: completed.
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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