The FDA Has Accepted GSK's Supplemental Marketing Application For Jemperli (Dostarlimab) Plus Chemotherapy For Adult Patients With Mismatch Repair Deficient/Microsatellite Instability-high Primary Advanced Or Recurrent Endometrial Cancer.
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The FDA has accepted GSK's supplemental marketing application for Jemperli (dostarlimab) plus chemotherapy for adult patients with mismatch repair deficient/microsatellite instability-high primary advanced or recurrent endometrial cancer. The PDUFA date is set for 23 September under priority review.
June 06, 2023 | 10:19 am
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GSK's Jemperli marketing application has been accepted by the FDA, potentially expanding the drug's market and increasing revenues.
The FDA's acceptance of GSK's supplemental marketing application for Jemperli indicates a positive step towards the drug's approval for endometrial cancer treatment. This could potentially expand the market for Jemperli and increase GSK's revenues, leading to a positive short-term impact on the company's stock price.
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