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Roche gets USFDA nod for VENTANA MMR RxDx Panel
Basel: Roche has recently announced that U.S. Food and Drug Administration (USFDA) has approved the VENTANA MMR RxDx Panel, the first companion diagnostic test to aid in identifying patients whose solid tumours are deficient in DNA mismatch repair (MMR), who may be eligible for JEMPERLI (dostarlimab-gxly) monotherapy, an anti-PD-1 immunotherapy from GSK.
The test evaluates a panel of MMR proteins in tumours to provide important treatment information to clinicians.
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751