A US Food and Drug Administration advisory panel on Friday recommended approval of a new drug that treats certain leukaemias when other treatments have failed, the Associated Press reported.
The drug, known as Sprycel, would be used to treat chronic myeloid leukaemia (CML) in patients who have developed a resistance or intolerance to Gleevec. CML represents 14 percent of all adult leukaemia's, according to the FDA.
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Bristol-Myers Squibb, which makes Sprycel, also got the panel's blessing to use the drug to treat Philadelphia chromosome-positive acute lymphoblastic leukaemia, the AP reported.
The FDA is expected to decide whether to approve Sprycel by June 28; the advisory panel met in Atlanta to coincide with the American Society of Clinical Oncology (ASCO) annual meeting, which is being held in that same city. (HealthDayNews)
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