Working with the pharmaceutical industry
Find out how we work with the pharmaceutical industry
Read moreNASS works closely with the National Institute for Health and Care Excellence and Scottish Medicines Consortium, contributing to the development of the Guideline and Quality Standard for Spondyloarthritis, and offering patient perspective on drug appraisals
The Spondyloarthritis Guideline was published in February 2017 and covers both axial SpA (AS) and peripheral spondyloarthritis.
The guideline includes recommendations on:
In June 2018, following on from the publication of the NICE Spondyloarthritis Guideline, NICE published a Quality Standard for Spondyloarthritis.
A Quality Standard sets out the priority areas for quality improvement in health and social care. They cover areas where there is variation in care. Each standard gives:
The NICE Quality Standard for Spondyloarthritis covers four areas:
NASS works closely with NICE to ensure the best possible range of medications are available in England, Wales and Northern Ireland.
Under the current NICE anti TNF guidance:
Treatment with another anti TNF is recommended for people who cannot tolerate, or whose disease has not responded to, treatment with the first TNF-alpha inhibitor, or whose disease has stopped responding after an initial response.
Read the full guidance
IL17a inhibitors
NICE published Guidance in 2016 recommending secukinumab (Cosentyx) as an option for treating active ankylosing spondylitis in adults whose disease has responded inadequately to conventional therapy (non-steroidal anti-inflammatory drugs) or TNF-alpha inhibitors. In 2021 it was also approved for non-radiographic axial SpA.
A further IL17a inhibitor, ixekizumab (Taltz) was also approved in 2021 for both non-radiographic axial SpA and ankylosing spondylitis.
These drugs work by limiting the action of Janus kinase enzymes, which are involved in the inflammation that causes the symptoms of axial spondyloarthritis.
England, Wales and Northern Ireland
The National Institute for Health and Care Excellence (NICE) approved the use of the JAK inhibitor upadacitinib, also known by the brand name, Rinvoq, on 30 September 2022 for treating active ankylosing spondylitis that is not controlled well enough with conventional therapy in adults.
NICE then approved upadacitinib (Rinvoq) or treating active non-radiographic axial spondyloarthritis in adults on 01 February 2023.
NICE guidance covers England, Wales and Northern Ireland.
Scotland
Upadacitinib (Rinvoq) has been approved by the Scottish Medicines Consortium for treating active non radiographic axial spondyloarthritis and active ankylosing spondylitis in adults who have responded inadequately to conventional therapy.
Another JAK inhibitor called tofacitinib (Xeljanz) has also been accepted for use within NHS Scotland for treating active ankylosing spondylitis in adults who have responded inadequately to conventional therapy.
Find out how we work with the pharmaceutical industry
Read moreTwo types of biologic therapy have been licensed to treat axial SpA (AS) by NICE. Both work by reducing inflammation produced by the body
Read moreBiosimilar medicines are developed to be highly similar to a biologic medicine
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