Bristol-Myers Squibb Company Release: Phase 3 Study Evaluating Yervoy® (Ipilimumab) For Melanoma In An Adjuvant Setting Meets Primary Endpoint Of Recurrence-Free Survival

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PRINCETON, N.J.--(BUSINESS WIRE)--Bristol-Myers Squibb Company (NYSE:BMY) today announced results from a Phase 3 randomized, double blind study demonstrating that Yervoy (ipilimumab) 10 mg/kg (n=475) significantly improved recurrence-free survival (RFS, the length of time before recurrence or death) vs. placebo (n=476) for patients with stage 3 melanoma who are at high risk of recurrence following complete surgical resection, an adjuvant setting.

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