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EMA looks to follow the FDA in limiting use of certain immune-regulating drugs

EMA follows FDA in scrutinizing safety of certain immune drugs

SMC OKs three new meds in latest decisions

NICE publishes final guidance backing Jyseleca for rheumatoid arthritis

NICE publishes final guidance backing Jyseleca for rheumatoid arthritis 21st January 2021 The National Institute for Health and Care Excellence (NICE) has published its final appraisal determination (FAD) recommending the use of Gilead Sciences and Galapagos’ Jyseleca (filgotinib) for the treatment of rheumatoid arthritis (RA). The FAD means that the daily oral pill will now be available on the NHS in England for the treatment of eligible adults patients with moderate-to-severe active RA. To be eligible, patients with moderate-to-severe RA will have had an inadequate response to intensive therapy with two or more disease-modifying anti-rheumatic drugs (DMARDs). Over 400,000 people in the UK live with RA – a degenerative auto-immune disease that can potentially cause life-threatening complications.

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