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Study identifier: NCT06037811 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Early Adalimumab Induction for Immune Checkpoint Inhibitor Associated Inflammatory Arthritis

Condition: Inflammatory Arthritis · Immune-related Adverse Event  ·  Sponsor: Tom Appleton

PhasePhase 2
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study will examine the effectiveness of administering adalimumab as a treatment for patients in the early stages of steroid-dependent immune checkpoint Inhibitor associated inflammatory arthritis (ir-IA). Adalimumab (ADA) is a TNF inhibitor (TNFi) that is well established as a standard of care treatment for numerous types of inflammatory arthritis. It is hoped that adalimumab at the early stages of the ir-IA will reduce the symptoms and therefore reduce the need for steroids. This study is a pragmatic randomized clinical trial. Patients will be randomized 1:1 to each treatment group. To evaluate the steroid sparing effect of early induction six doses of Adalimumab will be administered to patients in the study treatment arm as compared to the usual standard of care of a predefined corticosteroid regimen and taper at 12 weeks administered in the control group.

This description comes directly from the study's public registry record.

Talk to the study team

Tom Appleton, MD, PhD, FRCPC  ·  519-646-6100  ·  tom.appelton@sjhc.london.on.ca

Always discuss trial participation with your own doctor first.

Locations (1)

St. Joseph's Health CareLondon, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06037811