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Study of Safety and Efficacy of MY008211A in Paroxysmal Nocturnal Hemoglobinuria (PNH) Patients Who Are Naive to Complement Inhibitor Therapy
Sponsor: Wuhan Createrna Science and Technology Co., Ltd
Summary
The main purpose of this study is to evaluate the efficacy of MY008211A compared to eculizumab in PNH patients.
Official title: A Randomized, Multicenter, Active-comparator Controlled, Open-label Trial to Evaluate Efficacy and Safety of MY008211A Tablets in PNH Patients Who Are Naive to Complement Inhibitor Therapy
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
66
Start Date
2024-08-30
Completion Date
2025-12-30
Last Updated
2025-05-09
Healthy Volunteers
No
Interventions
MY008211A tablets
Participants will receive MY008211A at a dose of 400 mg orally b.i.d for 24 weeks
Eculizumab Injection
Eculizumab Injection for 24 weeks
Locations (2)
Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
Chinese Academy of Medical Sciences Hematology Hospital
Tianjin, Tianjin Municipality, China