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
A Phase 3, Double-blind, Placebo-controlled Study Evaluating Efficacy and Safety of Riliprubart in Participants With Refractory Chronic Inflammatory Demyelinating Polyneuropathy
Sanofi
140 participants
Jul 12, 2024
INTERVENTIONAL
Conditions
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.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Pharmaceutical form: Solution Route of administration: IV Infusion
Pharmaceutical form: Solution Route of administration: IV Infusion
Pharmaceutical form: Solution Route of administration: SC Injection
Pharmaceutical form: Solution Route of administration: SC Injection
Locations(131)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06290128