RIMRA is a prospective, longitudinal, observational study including patients with de novo symptoms of rheumatic disease or a flare of established rheumatic disease after treatment with an immune check point inhibitor. The aim of the study is to describe the clinical presentation, disease course and outcome of rheumatic irAEs in patients treated with immune check point inhibitors.
Study Type
OBSERVATIONAL
Enrollment
69
Antiinflammatory/DMARDs
Ålesund Hospital
Ålesund, Norway
Hospital of Southern Norway Trust
Kristiansand, Norway
Levanger Hospital
Levanger, Norway
Diakonhjemmet Hospital
Oslo, Norway
University Hospital of North Norway
Swollen joint count
Numbers (0-66)
Time frame: 1 year follow-up
C reactive protein
mg/L
Time frame: 1 year
Proportion of pateints with arthritis after one year
Time frame: 1 year
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Tromsø, Norway