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Genmab and Seagen Announce That TIVDAK® (tisotumab vedotin-tftv) Met its Primary Endpoint of Improved Overall Survival in Patients with Recurrent or Metastatic Cervical Cancer Compared to Chemotherapy - Vimarsana News

Genmab and Seagen Announce That TIVDAK® (tisotumab vedotin-tftv) Met its Primary Endpoint of Improved Overall Survival in Patients with Recurrent or Metastatic Cervical Cancer Compared to Chemotherapy

Company Announcement Phase 3 innovaTV 301 confirmatory trial met its primary endpoint of improved overall survival at predetermined, independent interim analysisTrial results to be submitted for...

Seagen and Genmab Announce TIVDAK® (tisotumab vedotin-tftv) Improved Overall Survival in Patients With Recurrent or Metastatic Cervical Cancer Compared With Chemotherapy Alone - Vimarsana News

Seagen and Genmab Announce TIVDAK® (tisotumab vedotin-tftv) Improved Overall Survival in Patients With Recurrent or Metastatic Cervical Cancer Compared With Chemotherapy Alone

Seagen Inc. and Genmab A/S announced today that the Phase 3 innovaTV 301 global trial in recurrent or metastatic cervical cancer patients with disease progression on or after front-line therapy who...

HPV Rates Skyrocket Despite Safe, Effective Vaccine - Vimarsana News

HPV Rates Skyrocket Despite Safe, Effective Vaccine

An epidemic of sexually transmitted HPV is now swirling around the US and the UK. Some serious cases have led to oropharyngeal cancer, which can affect the back of the throat, tonsils, and tongue.

Docs Steer Camera Through Stomach 'Like a Little Mars Rover' - Vimarsana News

Docs Steer Camera Through Stomach 'Like a Little Mars Rover'

New magnetic tech allows physicians to perform guided endoscopy to detect gastric illnesses much earlier.

U.S. FDA Broadens Indication for Verzenio® (abemaciclib) in HR+, HER2-, Node-Positive, High Risk Early Breast Cancer - Vimarsana News

U.S. FDA Broadens Indication for Verzenio® (abemaciclib) in HR+, HER2-, Node-Positive, High Risk Early Breast Cancer

/PRNewswire/ -- Eli Lilly and Company (NYSE: LLY) today announced that the U.S. Food and Drug Administration (FDA) approved an expanded indication for...