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Abbvie Announces U.S. Food And Drug Administration (FDA) And European Medicines Agency (EMA) Updates For Epcoritamab (EPKINLY®/TEPKINLY®) For The Trea...

Abbvie Announces U.S. Food And Drug Administration (FDA) And European Medicines Agency (EMA) Updates For Epcoritamab (EPKINLY®/TEPKINLY®) For The Trea...
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AbbVie Announces U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) Updates for Epcoritamab (EPKINLY®/TEPKINLY®) for the Treatment of Relapsed/Refractory Follicular Lymphoma

/PRNewswire/ AbbVie (NYSE: ABBV) today announced updates from the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) for. ....

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AbbVie Presents Results from Phase 3 CANOVA Study of Venetoclax in Patients with Relapsed or Refractory Multiple Myeloma

AbbVie (NYSE: ABBV) today announced data from its Phase 3 CANOVA study evaluating the safety and efficacy of venetoclax (VENCLEXTA®/ VENCLYXTO®) plus dexamethasone (VenDex) for patients with t(11;14)-positive relapsed or refractory (R/R) multiple myeloma who have received two or more prior treatments. Data did not . ....

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AbbVie Presents Results from Phase 3 CANOVA Study of Venetoclax in Patients with Relapsed or Refractory Multiple Myeloma

AbbVie Presents Results from Phase 3 CANOVA Study of Venetoclax in Patients with Relapsed or Refractory Multiple Myeloma
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AbbVie (ABBV) Reports Results from Phase 3 CANOVA Study of Venetoclax

AbbVie (ABBV) Reports Results from Phase 3 CANOVA Study of Venetoclax
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