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0 0 0.00292196631144726 0.00309384668270883 0.00223444482640087 -0.0161567548985905 -0.0227741491921622 -0.0267273977311791
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Bristol Myers Squibb Receives Positive CHMP Opinion for Opdivo® (nivolumab) plus Yervoy® (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability–High or...

Bristol-Myers Squibb Company (BMY) 
Last bristol-myers squibb company earnings: 2/6 07:05 am Check Earnings Report
US:NYSE Investor Relations: bms.com/investors.html
Company Research Source: Yahoo! Fin
statistically significant and clinically meaningful improvement in progression-free survival compared to investigator's choice of chemotherapy PRINCETON, N.J., November 15, 2024 BUSINESS WIRE Bristol Myers Squibb (NYSE: BMY) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended approval of Opdivo ® (nivolumab) plus Yervoy ® (ipilimumab) for the first-line treatment of adult patients with microsatellite instability–high (MSI-H) or mismatch repair deficient (dMMR) unresectable or metastatic colorectal cancer (mCRC). Of significance, the CheckMate -8HW trial results showed reduction in the risk of disease progression or death by 79% (HR: 0.21; 95% CI: 0.14-0.32; pEuropean Commission (EC), which has the authority to approve medicines for the European Union (EU), will now review the recommendation and make their decision. "Approximately 5-7% of metastatic colorectal cancer patients have dMMR or MSI-H tumors Show less Read more
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