New indication for Roferon-A approved in EU
The European Commission has approved Hoffmann-La Roche's Roferon-A(interferon alfa-2a) for the adjuvant treatment of malignant melanoma patients at risk of relapse following resection of the primary tumor. In Phase III studies, Roferon-A treatment was associated with a 25% reduction in the risk of relapse. The drug is currently approved in Europe for a number of indications including chronic myelogenous leukemia, cutaneous T cell lymphoma and renal cell carcinoma. Roche is also developing a pegylated version of interferon alfa-2a, called Pegasys, which is in late-stage hepatitis C trials.
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