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Tisotumab Vedotin Marketing Authorization Application Validated by European Medicines Agency for Treatment of Recurrent or Metastatic Cervical Cancer | Antibodies

Tisotumab Vedotin Marketing Authorization Application Validated by European Medicines Agency for Treatment of Recurrent or Metastatic Cervical Cancer ....

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EMA Validates MAA for Tisotumab Vedotin in Recurrent or Metastatic Cervical Cancer

The MAA seeking the approval of tisotumab vedotin in select patients with recurrent or metastatic cervical cancer has been validated by the EMA. ....

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Genmab A/S: Tisotumab Vedotin Marketing Authorization Application Validated by European Medicines Agency for Treatment of Recurrent or Metastatic Cervical Cancer

Genmab A/S: Tisotumab Vedotin Marketing Authorization Application Validated by European Medicines Agency for Treatment of Recurrent or Metastatic Cervical Cancer
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Tisotumab Vedotin Marketing Authorization Application Validated By European Medicines Agency For Treatment Of Recurrent Or Metastatic Cervical Cancer

Tisotumab Vedotin Marketing Authorization Application Validated By European Medicines Agency For Treatment Of Recurrent Or Metastatic Cervical Cancer
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Genmab: EMA To Review MAA Of Tisotumab Vedotin

Genmab A/S (GMAB) and Pfizer, Inc. (PFE) announced the European Medicines Agency has validated for review the marketing authorization application of tisotumab vedotin, an antibody-drug conjugate, developed for the treatment of adult patients with recurrent or metastatic cervical cancer with disease progression on or after systemic therapy. ....

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