drugset / Trial / NCT04654468

A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) Not Previously Treated With Complement Inhibition

NCT04654468

Phase 3 Active not recruiting 51 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

This study will enroll participants aged 12 years or older with a body weight ≥ 40 kilograms (kg) diagnosed with PNH who have not been previously treated with complement inhibitor therapy. Approximately 50 participants will be treated with Crovalimab for at least 24 weeks.

Timeline

Start
2021-03-17
Primary completion
2022-02-10
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Crovalimab Monoclonal antibody 680 mg Intravenous
Subject Crovalimab Monoclonal antibody 1020 mg Intravenous