drugset / Trial / NCT05935215

Efficacy and Safety of Switching From Anti-C5 Antibody Treatment to Iptacopan Treatment in Study Participants With Atypical Hemolytic Uremic Syndrome (aHUS)

NCT05935215

Phase 3 Recruiting 50 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this Phase 3 study is to evaluate the efficacy and safety of iptacopan upon switching from anti-C5 antibody to iptacopan treatment in study participants with aHUS.

Timeline

Start
2024-02-28
Primary completion
2028-07-21
Completion
2029-07-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Iptacopan Small molecule 200 mg