Skip to main content

bendamustine (Levact®)

 

Following non-submission

AWMSG advice

Status: Not endorsed (Statement of Advice)

In the absence of a submission from the holder of the marketing authorisation, bendamustine (Levact®) cannot be endorsed for use within NHS Wales for the front line treatment of multiple myeloma (Durie-Salmon stage II with progress or stage III) in combination with prednisone for patients older than 65 years who are not eligible for autologous stem cell transplantation and who have clinical neuropathy at time of diagnosis precluding the use of thalidomide or bortezomib containing treatment.

 Statement of Advice (SOA) bedamustine (Levact) 598 (PDF, 45Kb)

Medicine details

Medicine name bendamustine (Levact®)
Formulation 2.5 mg/ml powder for concentrate for solution for infusion
Reference number 598
Indication

For the front line treatment of multiple myeloma (Durie-Salmon stage II with progress or stage III) in combination with prednisone for patients older than 65 years who are not eligible for autologous stem cell transplantation and who have clinical neuropathy at time of diagnosis precluding the use of thalidomide or bortezomib containing treatment.

Company Napp Pharmaceuticals Ltd
BNF chapter Malignant disease & immunosuppression
Submission type Non-submission
Status Not endorsed (Statement of Advice)
Date of issue 05/11/2010
Follow AWTTC: