The FDA Has Accepted Bristol Myers Squibb's Supplemental Biologics License Application For Opdivo (Nivolumab) Plus Yervoy (Ipilimumab) As Potential First-line Treatment For Adult Patients With Unresectable Hepatocellular Carcinoma, With Prescription Drug User Fee Act Goal Date Of April 21, 2025
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The FDA has accepted Bristol Myers Squibb's application for Opdivo and Yervoy as a potential first-line treatment for unresectable hepatocellular carcinoma, with a decision expected by April 21, 2025.
August 21, 2024 | 11:04 am
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Bristol Myers Squibb's application for Opdivo and Yervoy as a first-line treatment for liver cancer has been accepted by the FDA, with a decision due by April 2025.
The acceptance of the application by the FDA is a positive regulatory step for Bristol Myers Squibb, indicating potential future revenue from these drugs if approved. This news is likely to have a positive short-term impact on BMY's stock price as it reflects progress in their drug development pipeline.
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