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infliximab (Remicade®)

 

Status: Superseded

AWMSG ADVICE SUPERSEDED BY NICE GUIDANCE ISSUED FEBRUARY 2015.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): infliximab (Remicade) 931 (PDF, 158Kb)

Medicine details

Medicine name infliximab (Remicade®)
Formulation 100 mg powder for concentrate for solution for infusion
Reference number 931
Indication

Treatment of severely active ulcerative colitis, in children and adolescents aged 6 to 17 years, 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
Assessment type Non-submission
Status Superseded
Ratification by Welsh Government 23/07/2012
Date of issue 27/07/2012
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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