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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

Active, not recruiting · Phase 3 · NCT06290128

Conditions: Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Polyneuropathy, Inflammatory Demyelinating, Chronic

At a glance

Research payments reported, 2025
$678,914
U.S. investigators named
19
Sites paid
20
Planned or actual enrollment
109

About the trial

Sponsor
Sanofi
Tested
Riliprubart (drug), Placebo (drug), Riliprubart (drug), Placebo (drug)
Dates
Started 2024-07-12; completion 2027-10-31
Results posted
Not yet

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.

From ClinicalTrials.gov, last updated 2026-08-10. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $678,914 in research payments for this study in 2025 (42 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.