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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)

Recruiting · Phase 3 · NCT06290141

Conditions: Chronic Inflammatory Demyelinating Polyneuropathy

At a glance

Research payments reported, 2025
$703,523
U.S. investigators named
20
Sites paid
23
Planned or actual enrollment
160

About the trial

Sponsor
Sanofi
Tested
riliprubart (drug), Placebo (drug), riliprubart (drug), Placebo (drug), IVIg (drug), Placebo (drug)
Dates
Started 2024-08-21; completion 2029-01-12
Results posted
Not yet

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.

From ClinicalTrials.gov, last updated 2026-10-19. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $703,523 in research payments for this study in 2025 (57 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.