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Rheumatic IMmune-Related Adverse Events in Patients Treated With Immune Check Point Inhibitors — RIMRA  

Immune-related Adverse Event Clinical Trial

Official title:
Rheumatic IMmune-Related Adverse Events in Patients Treated With Immune Check Point Inhibitors - a Prospective Observational Study

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05544292
Study type Observational
Source Diakonhjemmet Hospital
Contact Marte S Heiberg, MD, PhD
Phone 004722454086
Email marte.schrumpf@diakonsyk.no
Status Recruiting
Phase
Start date March 5, 2018
Completion date December 31, 2025
View Details
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