Overview

A Study to Test the Efficacy and Safety of Riliprubart Against the Usual Treatment of Intravenous Immunoglobulin (IVIg) in People With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Status:
RECRUITING
Trial end date:
2027-11-19
Target enrollment:
Participant gender:
Summary
The purpose of the study is to evaluate efficacy of riliprubart compared to IVIg in adult participants with CIDP who are receiving maintenance treatment with IVIg. The study duration will be for a maximum of 109 weeks including screening, treatment phases, and follow-up.
Phase:
PHASE3
Details
Lead Sponsor:
Sanofi
Treatments:
Immunoglobulins, Intravenous