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  • US FDA accepts Roche’s supplemental biologics licence application pharmaceutical-technology
    January 13, 2017
    The US Food and Drug Administration (FDA) has accepted Roche’s supplemental Biologics Licence Application (sBLA) and granted priority review for Tecentriq (atezolizumab) to treat people with locally advanced or metastatic urothelial carcinoma (mUC).

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