Clinical Trial

Study of Safety and Efficacy of MY008211A in Paroxysmal Nocturnal Hemoglobinuria (PNH) Patients Who Are Naive to Complement Inhibitor Therapy

Recruiting Phase 3
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Record status
This record was last updated May 9, 2025 (before its estimated December 30, 2025 completion). Its status may not reflect the trial's current state.
Summary
The main purpose of this study is to evaluate the efficacy of MY008211A compared to eculizumab in PNH patients.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-04-16.
Trial Details
NCT Number NCT06932744
Lead Sponsor Wuhan Createrna Science and Technology Co., Ltd
Conditions Paroxysmal Nocturnal Haemoglobinuria (PNH)
Enrollment 66 participants
Start Date 2024-08-30
Primary Completion 2025-12-30 (estimated)
Study Completion 2025-12-30 (estimated)
Updated on ClinicalTrials.gov 2025-05-09