Bristol Myers Squibb Receives European Commission Approval For Opdivo As Adjuvant Treatment For Patients With Completely Resected Stage IIB Or IIC Melanoma
Portfolio Pulse from Benzinga Newsdesk
Bristol Myers Squibb has received approval from the European Commission for Opdivo, a treatment for patients with completely resected stage IIB or IIC melanoma.
August 22, 2023 | 8:18 pm
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The approval of Opdivo by the European Commission could potentially increase Bristol Myers Squibb's market share and revenues in the European healthcare sector.
The approval of a new drug in a large market like Europe usually leads to increased sales and revenues for the manufacturing company. This could potentially increase Bristol Myers Squibb's stock price in the short term.
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