Study identifier:D7414C00001
ClinicalTrials.gov identifier:NCT05886244
EudraCT identifier:N/A
CTIS identifier:N/A
Open-Label, Multicenter Study to Assess the Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Eculizumab in Complement Inhibitor Treatment Naïve Adult Participants with Paroxysmal Nocturnal Hemoglobinuria (PNH) in China
paroxysmal nocturnal hemoglobinuria
Phase 3
No
Eculizumab
All
25
Interventional
18 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Aug 2024 by Alexion Pharmaceuticals, Inc.
Alexion Pharmaceuticals, Inc.
AstraZeneca
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Eculizumab Eculizumab will be administered by IV infusion. | - |