Skip to main content

ravulizumab (Ultomiris®)

 

Status: Excluded due to NICE appraisal

Product meets AWMSG exclusion criteria due to NICE appraisal TA698: Ravulizumab for treating paroxysmal nocturnal haemoglobinuria

Medicine details

Medicine name ravulizumab (Ultomiris®)
Formulation 300 mg concentrate for solution for infusion
Reference number 3495
Indication

Treatment of adult patients with paroxysmal nocturnal haemoglobinuria: in patients with haemolysis with clinical symptom(s) indicative of high disease activity; in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months

Company Alexion Pharma UK Ltd
BNF chapter Nutrition & blood
Assessment type N/A
Status Excluded due to NICE appraisal
Date of issue 02/07/2020
NICE guidance

TA698: Ravulizumab for treating paroxysmal nocturnal haemoglobinuria

Follow AWTTC: