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ibritumomab tiuxetan (Zevalin®)

 

Following non-submission

AWMSG advice

Status: Not endorsed (Statement of Advice)

Ibritumomab tiuxetan (Zevalin®) has not been endorsed for use within NHS Wales as consolidation therapy after remission induction in previously untreated patients with follicular lymphoma. The holder of the marketing authorisation is not in a position to progress a submission to AWMSG for the appraisal of ibritumomab tiuxetan (Zevalin®) for the above indication. As a result, AWMSG cannot provide advice to the Minister for Health and Social Services.

 Statement of Advice (SOA): ibritumomab tiuxetan (Zevalin) 159 (PDF, 46Kb)

Medicine details

Medicine name ibritumomab tiuxetan (Zevalin®)
Formulation 1.6 mg/ml radiopharmaceutical preparations for infusion
Reference number 159
Indication

Consolidation therapy after remission induction in previously untreated patients with follicular lymphoma. 

Company Bayer Healthcare Pharmaceuticals
BNF chapter Malignant disease & immunosuppression
Assessment type Non-submission
Status Not endorsed (Statement of Advice)
Date of issue 18/05/2009
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