Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06543459Phase 1Not yet recruiting
Phase 1, randomised, double-blind trial of MY-008 in paroxysmal nocturnal hemoglobinuria (PNH), sponsored by Wuhan Createrna Science and Technology Co., Ltd. Primary endpoint: Change from baseline in QTcF corrected for placebo up to 2 weeks. Planned start Aug 2024; 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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