The Cancer Letter

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Drugs & Targets

European Commission grants marketing authorization for Tepkinly + R2 in R/R FL

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The European Commission granted marketing authorization for Tepkinly (epcoritamab) in combination with lenalidomide and rituximab (Tepkinly + R2) for the treatment of adult patients with relapsed or refractory follicular lymphoma. The approval is based on results from the pivotal phase III EPCORE FL-1 trial that evaluated fixed-duration Tepkinly + R2 compared to standard of care R2.

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