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Rheumatic IMmune-Related Adverse Events in Patients Treated With Immune Check Point Inhibitors - a Prospective Observational Study
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Ålesund Hospital
Ålesund, Norway
Hospital of Southern Norway Trust
Kristiansand, Norway
Levanger Hospital
Levanger, Norway
Diakonhjemmet Hospital
Oslo, Norway
University Hospital of North Norway
Tromsø, Norway
Start Date
March 5, 2018
Primary Completion Date
December 31, 2024
Completion Date
December 31, 2024
Last Updated
August 24, 2025
69
ACTUAL participants
Antiinflammatory/DMARDs
OTHER
Lead Sponsor
Diakonhjemmet Hospital
Collaborators
NCT07453342
NCT05813418
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05832606