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golimumab (Simponi®)

 

Status: Excluded due to NICE appraisal

Product meets AWMSG exclusion criteria due to NICE appraisal TA375: Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed

Medicine details

Medicine name golimumab (Simponi®)
Formulation 50 mg solution for injection
Reference number 44
Indication

In combination with methotrexate (MTX) for the treatment of moderate to severe active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drug therapy including MTX has been inadequate. Golimumab has also been shown to improve physical function in this patient population

Company Merck Sharp & Dohme Ltd
BNF chapter Musculoskeletal & joint diseases
Assessment type N/A
Status Excluded due to NICE appraisal
Date of issue 29/04/2010
NICE guidance

TA375: Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed

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