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EULAR: Systemic JIA, adult-onset Still s disease are the same disease

EULAR: Systemic JIA, adult-onset Still s disease are the same disease
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Galapagos to showcase commitment to rheumatoid arthritis care at the upcoming European League Against Rheumatism congress

Investegate |Galapagos NV Announcements | Galapagos NV: Galapagos to showcase commitment to rheumatoid arthritis care at the upcoming European League Against Rheumatism congress

Investegate announcements from Galapagos NV, Galapagos to showcase commitment to rheumatoid arthritis care at the upcoming European League Against Rheumatism congress

Galapagos NV: Galapagos to showcase commitment to rheumatoid arthritis care at the upcoming European League Against Rheumatism congress

Celebrating EULAR's 75th anniversary with focus on a new era of rheumatoid arthritis care Mechelen, Belgium; 25 May 2022, 22.01 CET; Galapagos NV (Euronext & Nasdaq: GLPG) will

Investegate |Galapagos NV Announcements | Galapagos NV: Galapagos to present data on rheumatoid arthritis at the upcoming European League Against Rheumatism (EULAR) congress

ilgotinib Filgotinib is approved and marketed as Jyseleca (200mg and 100mg tablets) in the European Union, Great Britain, and Japan for the treatment of adults with moderate to severe active rheumatoid arthritis (RA) who have responded inadequately or are intolerant to one or more disease modifying anti-rheumatic drugs (DMARDs). Filgotinib may be used as monotherapy or in combination with methotrexate (MTX). The European Summary of Product Characteristics for filgotinib, which includes contraindications and special warnings and precautions, is available at www.ema.europa.eu. The interview form from the Japanese Ministry of Health, Labour and Welfare is available at www.info.pmda.go.jp. The Great Britain Summary of Product Characteristics is available at www.medicines.org.uk/emc. Applications have been submitted to the European Medicines Agency (EMA), the UK’s Medicines and Healthcare products Regulatory Agency (MHRA), and Japan’s Pharmaceuticals and Medical Devices Agency (PMDA

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