Skip to main content

ravulizumab (Ultomiris®)

 

Status: Excluded due to NICE appraisal

Product meets AWMSG exclusion criteria due to NICE appraisal TA941: Ravulizumab for treating AQP4 antibody-positive neuromyelitis optica spectrum disorder (terminated appraisal)

Medicine details

Medicine name ravulizumab (Ultomiris®)
Formulation 300 mg/3 ml and 1,100 mg/11 ml concentrate for solution for infusion
Reference number 5138
Indication

Treatent of neuromyelitis optica spectrum disorder (NMOSD) in adults who are anti-aquaporin-4-seropositive

Company Alexion Pharma UK Ltd
BNF chapter Malignant disease & immunosuppression
Assessment type N/A
Status Excluded due to NICE appraisal
Date of issue 19/12/2023
NICE guidance

TA941: Ravulizumab for treating AQP4 antibody-positive neuromyelitis optica spectrum disorder (terminated appraisal)

Follow AWTTC: