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ravulizumab (Ultomiris®)

 

Status: Excluded due to NICE appraisal

Product meets AWMSG exclusion criteria due to NICE appraisal TA940: Ravulizumab for treating generalised myasthenia gravis (terminated appraisal)

Medicine details

Medicine name ravulizumab (Ultomiris®)
Formulation intravenous infusion
Reference number 4940
Indication

Add-on to standard therapy for the treatment of adult patients with gMG who are anti-acetylcholine receptor (AChR) antibody-positive

Company Alexion Pharma UK Ltd
BNF chapter Immunological products & vaccines
Assessment type N/A
Status Excluded due to NICE appraisal
Date of issue 30/09/2022
NICE guidance

TA940: Ravulizumab for treating generalised myasthenia gravis (terminated appraisal)

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