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Genmab to Showcase Data in Various Patient Populations to be Presented at the American Society of Clinical Oncology (ASCO) Annual Meeting

Genmab to Showcase Data in Various Patient Populations to be Presented at the American Society of Clinical Oncology (ASCO) Annual Meeting
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United statesAndrew carlsenTisotumab vedotinAsia pacificDavid freundelJudith klimovskyAbbvie biotechnology ltdAmerican society of clinical oncologyExchange commissionProduct communicationsMeeting libraryClinical oncologyAnnual meetingExecutive vice presidentChief development officerNorth america

Genmab to Showcase Data in Various Patient Populations to be Presented at the American Society of Clinical Oncology (ASCO) Annual Meeting

Media ReleaseCOPENHAGEN, Denmark; May 23, 2024 Six oral and poster presentations will highlight breadth of clinical program and potential utility of epcoritamab-bysp in patients with.

United statesTisotumab vedotinDavid freundelAsia pacificJudith klimovskyAndrew carlsenProduct communicationsMeeting libraryExchange commissionAbbvie biotechnology ltdAmerican society of clinical oncologyClinical oncologyAnnual meetingExecutive vice presidentChief development officerNorth america

Genmab A/S: Genmab to Showcase Data in Various Patient Populations to be Presented at the American Society of Clinical Oncology (ASCO) Annual Meeting

Six oral and poster presentations will highlight breadth of clinical program and potential utility of epcoritamab-bysp in patients with difficult-to-treat lymphomas across multiple lines of therapy

United statesDavid freundelTisotumab vedotinAndrew carlsenAsia pacificJudith klimovskyGenmab us incProduct communicationsExchange commissionAbbvie biotechnology ltdMeeting libraryAmerican society of clinical oncologyClinical oncologyAnnual meetingExecutive vice presidentChief development officer

FDA-approved TIVDAK®: Targeting tissue factor in cervical cancer

FDA-approved TIVDAK®: Targeting tissue factor in cervical cancer
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Tisotumab vedotinSeagen incSino biological inc

Tisotumab Vedotin Gains Full FDA Approval for Recurrent or Metastatic Cervical Cancer

The FDA granted full approval for tisotumab vedotin-tftv to treat recurrent or metastatic cervical cancer that progressed after chemotherapy, offering patients improved overall survival and a manageable safety profile.

Tamika felderChris boshoffBrian slomovitzCervivor incImage creditCancer research committeeMount sinai medical centerMiami beachChief visionary officerTisotumab vedotin