drugset / Trial / NCT04958265

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

NCT04958265

Phase 3 Active not recruiting 41 enrolled Hoffmann-La Roche Chugai Pharmaceutical · collab
NaSingle-groupOpen-labelTreatment

Summary

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

Timeline

Start
2021-11-17
Primary completion
2025-07-04
Completion
2029-05-19

Drugs

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