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GSK’ Jemperli gets regular approval for dMMR endometrial cancer

On February 9, the Food and Drug Administration approved dostarlimab-gxly, or Jemperli, marketed by GlaxoSmithKline, for adult patients with mismatch repair deficient, or dMMR, recurrent or advanced endometrial cancer, as determined by an 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. In April 2021, dostarlimab-gxly received accelerated approval for adult patients with dMMR recurrent or advanced endometrial cancer, as determined by an FDA-approved test, that has progressed on or following a prior platinum-containing regimen. Reference Link

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