Infliximab

BNF:
10.1.3
Status:
Red
Decision Date:
None
 

Comments

Hospital use only.

Remicade (reference infliximab product), Remsima and Inflectra (biosimilars) are available. 

  • NICE TA329: for treating moderately to severely active ulcerative colitis after the failure of conventional therapy. (Decision date - March 2015)
  • NICE TA373: for treating juvenile idiopathic arthritis (Decision date - March 2015)
  • NICE TA375: for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed. (Decision date - February 2016)
  • NICE TA383: for ankylosing spondylitis and non-radiographic axial spondyloarthritis.  (Decision date - March 2016)
  • NICE TA715Adalimumab, etanercept and infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed. (Decision date - August 2021)
  • SSC2596: for refractory sarcoidosis (excluding neurosarcoidosis). NHSE commissioned. (Decision date - April 2024)

Red Drug Classifications

  • 1: Requiring specialist assessment to enable patient selection, initiation and ongoing treating
  • 2: Requiring long term on-going monitoring of efficacy by a specialist and not suitable for shared care
  • 3: Requiring long term on-going monitoring of toxicity by a specialist (either because of difficulty in recognising side effects or high cost of investigations to identify toxicity)

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