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BMS's Sprycel gets FDA priority review for newly diagnosed CML

This article was originally published in Scrip

Executive Summary

The supplemental NDA for Bristol-Myers Squibb/Otsuka Pharmaceutical's second generation BCR-ABL inhibitor Sprycel (dasatinib) for the treatment of newly diagnosed, chronic-phase chronic myeloid leukaemia (CML) has been accepted for filing by the US FDA and been granted a priority review designation.

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