drugset / Trial / NCT06290128

A Study to Test the Effects and Safety of Riliprubart in People With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) for Which the Usual Treatments do Not Work

NCT06290128

Phase 3 Recruiting 140 enrolled Sanofi
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate efficacy of riliprubart compared to placebo in adult participants with CIDP whose disease is refractory to standard of care. The study duration will be for a maximum of 111 weeks including screening, treatment phases, and follow-up.

Timeline

Start
2024-07-12
Primary completion
2027-05-17
Completion
2028-11-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Riliprubart Monoclonal antibody Intravenous