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golimumab (Simponi®)

 

Status: Superseded

AWMSG ADVICE SUPERSEDED BY NICE GUIDANCE ISSUED FEBRUARY 2015. Refer to TA329: Infliximab, adalimumab and golimumab for treating moderately to severely active ulcerative colitis after the failure of conventional therapy for full guidance on NICE recommendations, including any specific restrictions on the use of the technology. AWMSG documentation provided for reference only.

 Statement of Advice (SOA): golimumab (Simponi) 1323 (PDF, 157Kb)

Medicine details

Medicine name golimumab (Simponi®)
Formulation 50 mg solution for injection, 100 mg solution for injection
Reference number 1323
Indication

Treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies

Company Merck Sharp & Dohme Ltd
BNF chapter Gastro-intestinal system
Submission type Non-submission
Status Superseded
Ratification by Welsh Government 26/02/2014
Date of issue 27/02/2014
NICE guidance

TA329: Infliximab, adalimumab and golimumab for treating moderately to severely active ulcerative colitis after the failure of conventional therapy

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