Following non-submission
AWMSG advice |
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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. |
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Medicine details |
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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. |
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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 |