GlaxoSmithKline plc’s PD-1 blocking antibody, Jemperli (dostarlimab-gxly), has been approved for a second indication in the US, the treatment of adult patients with mismatch repair-deficient (dMMR) recurrent or advanced solid tumors that have progressed on or following prior treatment and who have no satisfactory alternative treatment options. This is a broader indication than the product’s first license for dMMR endometrial cancer, and marks the company’s continued drive to again become a major player in the cancer field.
Jemperli has been associated with a 41.6% objective response rate (ORR) in patients with dMMR solid tumors in the ongoing...
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