Bristol Myers Squibb announced the first presentation of results from the Phase 3 CheckMate -9DW trial evaluating the dual immunotherapy combination of Opdivo or nivolumab plus Yervoyor ipilimumab, compared to investigator’s choice of lenvatinib or sorafenib as a first-line treatment for patients with unresectable hepatocellular carcinoma HCC . Results from the study will be featured in a late-breaking oral presentation at the 2024 ASCO Annual Meeting today, June 4. “Despite recent advances in the treatment of HCC, prognosis remains poor for patients with advanced HCC, and therapies that improve survival and help delay disease progression are needed,” said Peter R. Galle, M.D., of the University Medical Center, Mainz. “These data from CheckMate -9DW confirm the efficacy of the combination of nivolumab and ipilimumab and ability to extend survival, which is very encouraging.” “The combination of Opdivo plus Yervoy has been an established second-line treatment for patients with advanced HCC and, with these results, we can demonstrate that Opdivo plus Yervoy significantly increases survival and other key efficacy measures in the first-line setting for patients with advanced disease,” said Dana Walker, M.D., M.S.C.E., vice president, global program lead, gastrointestinal and genitourinary cancers, Bristol Myers Squibb. “We look forward to discussing these data with health authorities and potentially bringing the dual immunotherapy combination of Opdivo plus Yervoy to more patients.”
Meet Your ETF AI Analyst
- Discover how TipRanks' ETF AI Analyst can help you make smarter investment decisions
- Explore ETFs TipRanks' users love and see what insights the ETF AI Analyst reveals about the ones you follow.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on BMY:
- UroGen Pharma announces David Lin as chief commercial officer
- Bristol Myers announces results from Phase 3 KRYSTAL-12 study
- Bristol Myers’ Breyanzi approved by FDA as new CAR T cell therapy in MCL
- Bristol Myers announces EC approves Opdivo combination
- Prothena announces Bristol Myers Squibb obtained exclusive PRX019 license
