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0.00358808754933625 0 -0.0039468963042698 -0.00932902762827406 -0.0102260495156082 -0.00466451381413703 -0.00574094007893793 -0.0010764262648009
Stock impact report

Genmab Announces Financial Results for the First Quarter of 2024

Genmab A/S - American Depositary Shares (GMAB) 
Company Research Source: GlobeNewswire
May 2, 2024 Copenhagen, Denmark; Interim Report for the First Quarter Ended March 31, 2024 Highlights The U.S. Food and Drug Administration (U.S. FDA) granted Priority Review for the supplemental Biologics License Application (sBLA) for EPKINLY® (epcoritamab-bysp) for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy, with a Prescription Drug User Fee Act (PDUFA) target action date of June 28, 2024An additional Phase 3 clinical trial was initiated, evaluating epcoritamab in combination with rituximab and lenalidomide compared to chemoimmunotherapy in previously untreated follicular lymphoma The U.S. FDA accepted for Priority Review the sBLA seeking to convert the accelerated approval of Tivdak® (tisotumab vedotin-tftv) to full approval, for the treatment of patients with recurrent or metastatic cervical cancer with disease progression on or after first-line therapyGenmab announced the decision of its arbi Show less Read more
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