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Roche’s Perjeta is one of the first drugs to take advantage of a new regulatory pathway in the US that is designed to get new drugs for early-stage breast cancer to market quicker.
Perjeta (pertuzumab) has been granted priority review by the FDA for use before surgery (neoadjuvant treatment) in women with HER2-positive breast cancer, setting it up for approval in the new indication by the end of October 2013.
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