GSK Jemperli gets US FDA full approval to treat patients with recurrent or advanced mismatch repair-deficient endometrial cancer
GSK plc reports that the US Food and Drug Administration (FDA) granted full approval for Jemperli (dostarlimab-gxly) for the treatment of adult patients with mismatch repair-deficient (dMMR) recurrent or advanced endometrial cancer, as determined by a US FDA-approved test, that has progressed on or following a prior platinum-containing regimen in any setting and are not candidates for curative surgery or radiation. Hesham Abdullah, senior vice president, global head of oncology development, GSK, said:
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