Genmab Says European Commission Grants Marketing Authorization for Tivdak as Cervical Cancer Treatment
The company said the approval was based on data from a phase 3 trial that met its primary endpoint of overall survival, with Tivdak demonstrating a 30% reduction in risk of death compared with chemotherapy.
Tivdak, also known as tisotumab vedotin, is co-developed and co-commercialized by
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Genmab Says European Commission Grants Marketing Authorization for Tivdak as Cervical Cancer Treatment
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