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COMPLETED
NCT06578949
PHASE3

Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Ravulizumab in Chinese Adults Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH)

Sponsor: Alexion Pharmaceuticals, Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

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