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U.S. Food and Drug Administration Approves Opdivo® (nivolumab) plus Yervoy® (ipilimumab) as a First-Line Treatment for Unresectable or Metastatic Hepatocellular Carcinoma

1. FDA approves Opdivo plus Yervoy for metastatic liver cancer treatment. 2. This could significantly expand BMY's market potential in oncology.

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Why Very Bullish?

The FDA approval for Opdivo plus Yervoy strengthens BMY's oncology portfolio. Historical data shows that previous approvals for similar treatments often led to stock price increases.

How important is it?

The approval is a significant advancement for BMY and provides a competitive edge in the oncology market, indicating a likely positive long-term impact on stock performance.

Why Long Term?

The approval will likely increase sales over time as the treatment gains market acceptance, similar to previous oncology drug approvals that sustained revenue growth.

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PRINCETON, N.J.--(BUSINESS WIRE)---- $BMY #BMS--U.S. Food and Drug Administration Approves Opdivo plus Yervoy as a First-Line Treatment for Unresectable or Metastatic Hepatocellular Carcinoma.

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