The U.S. Food and Drug Administration (FDA) granted accelerated approval to Incyte Corp.'s Pemazyre (pemigatinib) as the first treatment approved for adults with certain types of previously treated, advanced cholangiocarcinoma, a cancer of bile ducts. While approving Pemazyre, the FDA considered the overall risk to benefit assessment for patients with tumors harboring FGFR2 gene fusions.
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