Sandra Horning, MD
The FDA has granted a priority review to a supplemental biologics license application (sBLA) for pertuzumab (Perjeta) for use in combination with trastuzumab (Herceptin) and chemotherapy for the adjuvant treatment of patients with HER2-positive early breast cancer.
“We are pleased to receive priority review for the Perjeta-based regimen for the adjuvant treatment of HER2-positive early breast cancer,” Sandra Horning, MD, chief medical officer and head of Global Product Development, Genentech, said in a statement. “The goal of treating breast cancer early is to provide people with the best chance for a cure. Despite advances in the treatment of this disease, many people treated with the current standard of care still see their cancer return.”
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