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U.S. Food and Drug Administration (FDA) Accepts Bristol-Myers Squibb’s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) in Intermediate- and Poor-Risk Patients with Advanced Renal Cell Carcinoma and Grants Priority Review

17:28 EST 13 Dec 2017 | Businesswire

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The Opdivo plus Yervoy combination previously received FDA Breakthrough Therapy Designation Application based on results from phase 3 CheckMate -214 study Bristol-Myers Squibb Company (NYSE: BMY) announced to...

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Bristol-Myers Squibb
Media:
Audrey Abernathy, cell: 919-605-4521
audrey.abernathy@bms.com
or
Investors:
Tim Power, 609-252-7509
timothy.power@bms.com
or
Bill Szablewski, 609-252-5894
william.szablewski@bms.com

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