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. 2007 Apr;83(978):251–260. doi: 10.1136/pgmj.2006.052688

Table 3 Biologics approved for IMIDs: FDA, EMEA and NICE.

Biologic agent Action FDA licence EMEA licence NICE approval
Infliximab Anti‐TNFα RA RA RA
AS AS PsA
PsA PsA CD
CD CD AS (appraisal)
UC UC UC (submitted)
Paediatric CD Psoriasis Psoriasis
Paediatric CD (appraisal)
Etanercept Anti‐TNFα RA RA RA
JIA JIA JIA
AS AS PsA
PsA PsA Psoriasis
Psoriasis Psoriasis AS (appraisal)
Adalimumab Anti‐TNFα RA RA RA (appraisal)
PsA PsA PsA
AS AS AS
Rituximab Anti‐CD20 RA RA RA (submitted)
Abatacept CTLA4Ig RA RA (submitted) RA (submitted)
Efalizumab Anti‐CD11a Psoriasis Psoriasis Psoriasis
Alefacept LFA‐3/IgG Fc construct Psoriasis None None
Anakinra Anti‐IL1 RA RA None

AS, ankylosing spondylitis; CD, Crohn's disease; CTLA4, cytotoxic T lymphocyte antigen‐4; EMEA, European Medicines Agency; FDA, US Food and Drug Administration; IL, interleukin; JIA, juvenile idiopathic arthritis; NICE, UK National Institute for Health and Clinical Excellence; PsA, psoriatic arthritis; RA, rheumatoid arthritis; TNFα, tumour necrosis factor‐α; UC, ulcerative colitis.