Last reviewed · How we verify

NCT06578949

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

Completed Phase 3 Last updated 21 January 2026
What this trial tests

Phase 3 trial testing Ravulizumab in Paroxysmal Nocturnal Hemoglobinuria in 18 participants. Completed in 22 December 2025.

Timeline
10 October 2024
Primary endpoint
15 May 2025
22 December 2025

Quick facts

Lead sponsorAlexion Pharmaceuticals, Inc.
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment18
Start date10 October 2024
Primary completion15 May 2025
Estimated completion22 December 2025
Sites8 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Alexion Pharmaceuticals, Inc. — full company profile →

Who can join

18 and older, any sex, with Paroxysmal Nocturnal Hemoglobinuria or PNH. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to evaluate the efficacy of ravulizumab in adult participants with PNH.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Ravulizumab

Trials testing the same drug.

Other recruiting trials for Paroxysmal Nocturnal Hemoglobinuria

Currently open trials in the same condition.

Other Alexion Pharmaceuticals, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06578949.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing