drugset / Trial / NCT02946463

ALXN1210 (Ravulizumab) Versus Eculizumab in Complement Inhibitor Treatment-Naïve Adult Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH)

NCT02946463 ↗

Phase 3 Completed 272 enrolled Alexion Pharmaceuticals, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary purpose of this study was to assess the noninferiority of ravulizumab compared to eculizumab in adult participants with PNH who had never been treated with a complement inhibitor (treatment-naïve).

Timeline

Start
2016-12-12
Primary completion
2023-02-28
Completion
2023-02-28

Outcome

Met primary endpoint

paper Ravulizumab demonstrated noninferior efficacy and comparable safety to eculizumab in two open-label, phase 3 studies in patients with paroxysmal nocturnal hemoglobinuria (PNH) who complement inhibitor-naive (Study 301) or were previously treated with eculizumab (Study 302). PMID 32869125 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Eculizumab Monoclonal antibody 900 mg Intravenous
Subject Ravulizumab Monoclonal antibody 3000 mg Intravenous
Subject Ravulizumab Monoclonal antibody 3300 mg Intravenous
Subject Ravulizumab Monoclonal antibody 3600 mg Intravenous