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Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Ravulizumab in Chinese Adults Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Sponsor: Alexion Pharmaceuticals, Inc.
Summary
The primary objective of this study is to evaluate the efficacy of ravulizumab in adult participants with PNH.
Official title: A Phase 3, Single-arm, Open-label, Multicenter Study to Assess the Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Ravulizumab in Complement Inhibitor Treatment Naïve Adult Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) in China
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
18
Start Date
2024-10-10
Completion Date
2025-12-22
Last Updated
2026-06-05
Healthy Volunteers
No
Conditions
Interventions
Ravulizumab
Ravulizumab will be administered by intravenous (IV) infusion.
Locations (8)
Research Site
Beijing, China
Research Site
Guangzhou, China
Research Site
Hangzhou, China
Research Site
Nantong, China
Research Site
Shanghai, China
Research Site
Tianjin, China
Research Site
Tianjin, China
Research Site
Wuhan, China