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Study of Safety and Efficacy of MY008211A in Patients With Residual Anemia Despite Anti-C5 Antibody Treatment
Sponsor: Wuhan Createrna Science and Technology Co., Ltd
Summary
The main purpose of this study is to evaluate the efficacy of MY008211A in PNH patients with residual anemia despite treatment with anti-C5 antibody.
Official title: A Multicenter, Single-arm, Open-label Phase III Study to Evaluate Efficacy and Safety of MY008211A Tablets in Patients With PNH and Residual Anemia, Despite Treatment With Anti-C5 Antibody.
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2024-08-30
Completion Date
2025-12-30
Last Updated
2025-05-09
Healthy Volunteers
No
Conditions
Interventions
MY008211A tablets
MY008211A tablets Participants will receive MY008211A at a dose of 400 mg orally b.i.d
Locations (1)
Peking Union Medical College Hospital (PUMCH).
Beijing, Beijing Municipality, China