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  • NCT07412704

Not Yet Recruiting

A Study of BMS-986528 in Participants With Refractory Rheumatoid Arthritis - IM062-0001

Updated: 20 February, 2026   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
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Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.
Print this page IM062-0001
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Trial Details

  • Phase 1/Phase 2

    Phase

  • Gender(s)

  • 18-65

    Age Range

  • 17

    Location(s)

  • Not Yet Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Cohort A1
Drug: BMS-986528
Experimental: Cohort A2
Drug: BMS-986528
Experimental: Cohort A3
Drug: BMS-986528
Experimental: Cohort A4
Drug: BMS-986528
Experimental: Cohort A5
Drug: BMS-986528
Experimental: Cohort A6
Drug: BMS-986528
Experimental: Cohort A7
Drug: BMS-986528
Experimental: Cohort A8
Drug: BMS-986528
Experimental: Cohort B1
Drug: BMS-986528
Experimental: Cohort B2
Drug: BMS-986528

Key Eligibility Criteria

Inclusion Criteria - Adult participants with rheumatoid arthritis (RA) who meet definition of difficult-to-treat. Exclusion Criteria - Juvenile arthritis or onset of inflammatory arthritis before age 18. - Seronegative RA participants in whom polymyalgia rheumatica has not been ruled out. - Active fibromyalgia with pain symptoms or signs that would interfere with joint assessment. - Other protocol-defined Inclusion/Exclusion criteria apply.

If you want to report a side effect, you can report directly to the Danish Medicines Agency via the website www.meldenbivirkning.dk
We recommend that you also contact BMS to report side effects.
Side effects and other reportable events are defined here
Report side effects or product quality complaints: Medical Information

466-DK-2200001