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adalimumab (Humira®)

 

Following non-submission

AWMSG advice

Status: Not endorsed (Statement of Advice)

In the absence of a submission from the holder of the marketing authorisation, adalimumab (Humira®) cannot be endorsed for use within NHS Wales for the of treatment of moderately active Crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies.

 Statement of Advice (SOA): adalimumab (Humira) 1793 (PDF, 38Kb)

Medicine details

Medicine name adalimumab (Humira®)
Formulation 40 mg and 40 mg/8 ml solution for injection
Reference number 1793
Indication

Treatment of moderately active Crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies.

Company AbbVie Ltd
BNF chapter Musculoskeletal & joint diseases
Assessment type Non-submission
Status Not endorsed (Statement of Advice)
Date of issue 16/01/2013
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