drugset / Trial / NCT04861259

A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Adult and Adolescent Participants With Atypical Hemolytic Uremic Syndrome (aHUS)

NCT04861259

Phase 3 Active not recruiting 83 enrolled Hoffmann-La Roche Chugai Pharmaceutical · collab
NaSingle-groupOpen-labelTreatment

Summary

This study aims to evaluate the efficacy and safety of crovalimab in adult and adolescent participants with aHUS.

Timeline

Start
2021-10-22
Primary completion
2025-10-09
Completion
2029-08-20

Drugs

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