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FDA Approves Celgene’s Azacitidine for Juvenile Leukemia

May 20, 2022, 8:04 PM

FDA approves Bristol-Myers Squibb division Celgene’s Vidaza (azacitidine) for pediatric patients with newly diagnosed juvenile myelomonocytic leukemia.

NOTE

  • Bristol-Myers Squibb Co. shares were little changed in postmarket trading as of 4:01 p.m. New York time
    • The average 12-month price target of $78.63 is 3.2% above the current price
    • 14 buys, 6 holds, 2 sells

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To contact the reporter on this story:
Jim Silver in New York at jsilver@bloomberg.net

To contact the editor responsible for this story:
Sunil Kesur at skesur@bloomberg.net

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