EC extends label for Bayer HealthCare
The European Commission has extended the marketing authorization for German drugmaker Bayer HealthCare's Zevalin ([90Y]-ibritumomab tiuxetan) to include its use as a first-line therapy after remission of induction in previously-untreated patients with follicular lymphoma. The EC's decision is based on strong data from the Phase III FIT study of the drug, which was first approved in 2004.
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