Data released at the European Society for Medical Oncology (ESMO) on Merck & Co., Inc.’s Keytruda strengthen the PD-1 inhibitor drug’s leading position in cervical cancer as the company moves the drug into the first-line setting. But Seagen Inc. and Genmab A/S’s newly approved antibody-drug conjugate (ADC) Tivdak (tisotumab vedotin-tftv) means increased competition in the second-line setting of a cancer that affects a small population.
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