Genentech Inc./Roche has strengthened its foothold in early breast cancer with a new supplementary US FDA approval for the rising HER2 franchise star Perjeta covering use in the adjuvant (after surgery) setting and full approval in the neoadjuvant (before surgery) line of therapy.
Roche Digs In To Early Breast Cancer With New Perjeta Approvals
Better than expected FDA labeling for rising star Perjeta in neoadjuvant (before surgery) and adjuvant (after surgery) breast cancer could boost sales greatly beyond expectations, some analysts say.
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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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