On April 29, the US Food and Drug Administration (FDA) granted traditional approval to tisotumab vedotin-tftv for recurrent or metastatic cervical cancer with disease progression on or after chemotherapy. Tisotumab vedotin-tftv previously received accelerated approval for this indication.
For more information read the FDA announcement and the Pfizer announcement.
Posted 4/30/2024
An at-home option for cervical cancer screening breaks down barriers to care and offers the same level of precision as screening in the clinic.
