Rheumatoid Arthritis: JAK Inhibitor Dose Tapering Study

We are exploring whether reducing the dose of JAK inhibitors helps maintain low disease activity in rheumatoid arthritis patients. This study will also look at the impact on pain, function, and overall quality of life.

What diseases are being studied?

Health conditions and diseases that the clinical trial is designed to study and treat.

Who can participate in the clinical trial?

These questions help us understand your situation so we can let the trial team know whether you might be a potential match. This is not a medical evaluation and is not part of the official screening, the study doctor will make the final decision..

What active substances are being studied?

Active substances that are officially approved for use in the European Union and considered safe by EMA. These substances are already on the market and may be tested for new conditions or populations.

Baricitinib
Baricitinib is a substance that reduces immune-driven inflammation to treat rheumatoid arthritis.
Filgotinib
Filgotinib is a substance that reduces inflammation and helps treat rheumatoid arthritis and other inflammatory joint conditions.
Tofacitinib
Tofacitinib is a substance that reduces immune system activity to treat inflammatory autoimmune conditions like rheumatoid arthritis and ulcerative colitis.

Where is the clinical trial being conducted?

Locations and medical facilities where this clinical trial is currently recruiting or conducting research. Select the locations where you would like to participate.

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Assistance Publique Hopitaux De Paris
Rheumatology
Angers, France
University Hospital Of Clermont-Ferrand
Rheumatology
Beaumont, France
Centre Hospitalier Universitaire De Bordeaux
Rheumatology
Bordeaux, France

Sponsor: Centre Hospitalier Universitaire De Toulouse
Last updated: Nov 26, 2025

Disclaimer: Parts of this content have been automatically extracted from the EU Clinical Trials registry. While we strive for accuracy, please always contact the trial site or sponsor directly for correct and official information before making any decisions about participation. View on EU Clinical Trials.