300 Participants Needed

Potential Treatment for Early Polymyalgia Rheumatica (PMR)

Recruiting at 15 trial locations

Trial Summary

What is the purpose of this trial?

This Phase 3 research study is evaluating an investigational study drug in adults with newly diagnosed or early relapsing polymyalgia rheumatica (PMR). The purpose of this study is to assess whether the investigational study drug affects PMR symptoms and steroid use in study participants. The investigational study drug is not approved by health authorities such as the US Food and Drug Administration (FDA) and is still under investigation for the treatment of PMR, so its effectiveness and safety have not been established. PMR is currently treated with corticosteroids like prednisone, which can cause side effects when used for long periods. This study is looking at whether an investigational study drug that targets inflammation associated with PMR may affect symptoms and steroid use. Intended for U.S. Audiences Only © 2026 Sanofi US Services, Inc. All Rights Reserved

Timeline

Screening

Participants are evaluated to confirm eligibility

Up to 6 weeks
1 Visit

Study Treatment Period

Participants receive the investigational study drug or placebo by injection every 2 weeks

52 weeks
12 Visits

Follow-up

Participants are monitored after completing study treatment

6 weeks
1 Visit

Find a Clinic Near You

Who Is Running the Clinical Trial?

Sanofi

Lead Sponsor