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)
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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
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BMY
Earnings
- 10/31/24 - Beat
BMY
Sec Filings
- 11/5/24 - Form 4
- 11/5/24 - Form 4
- 11/5/24 - Form 4
- BMY's page on the SEC website