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Post-Yervoy melanoma data at ESMO support BMS's Opdivo BLA

This article was originally published in Scrip

Executive Summary

Bristol-Myers Squibb revealed Phase III results in melanoma for the programmed cell death-1 (PD-1) inhibitor Opdivo (nivolumab) at the European Society for Medical Oncology (ESMO) meeting on 29 September that support the biologic license application (BLA) for which the US FDA recently granted priority review – data that may outshine Merck & Co's competing drug.



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