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Nov18
Genentech’s Herceptin® USFDA Approved for Adjuvant Treatment of HER2-Positive Node-Positive Breast Cancer
The USFDA has just approved Herceptin® of Genenetch, Inc. (NYSE:DNA) as part of a treatment regimen containing doxorubicin, cyclophosphamide and paclitaxel for the adjuvant treatment of HER2-positive node-positive breast cancer patients.
herceptin.gifAdjuvant therapy is given to women with early-stage (localized) breast cancer who have had initial treatment surgery with or without radiation therapy with the goal of reducing the risk of cancer recurrence and/or the occurrence of metastatic disease.

The said approval was based on an interim joint analysis of data from two Phase III clinical trials of more than 3, 500 patients.

Herceptin® is a targeted therapeutic antibody treatment for women who have tumors that overexpress the human epidermal growth factor receptor 2 (HER2) protein and is the only targeted biologic therapy approved for treatment of HER2-positive breast cancer in the adjuvant and metastatic settings.

Find more details from the Genentech press release.


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