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FDA grants accelerated approval of Perjeta for people with HER2-positive early stage
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10-02-2013, 05:00 AM
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FDA grants accelerated approval of Perjeta for people with HER2-positive early stage
The U.S. Food and Drug Administration granted accelerated approval of a Perjeta- (pertuzumab) regimen for neoadjuvant treatment (use before surgery) in people with high-risk, HER2-positive early stage breast cancer.
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