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Genmab (GMAB) FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab

Genmab (GMAB) FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab
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U.S. FDA Accepts For Priority Review The Supplemental Biologics License Application For Epcoritamab (EPKINLY®) For Difficult-To-Treat Relapsed Or Refr...

U.S. FDA Accepts For Priority Review The Supplemental Biologics License Application For Epcoritamab (EPKINLY®) For Difficult-To-Treat Relapsed Or Refr...
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Genmab A/S: U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma

Genmab A/S: U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma
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Alvotech and Teva Announce U.S. Approval of SIMLANDI®

SIMLANDI is the first citrate-free, high-concentration biosimilar to be designated interchangeable to Humira in the U.S. SIMLANDI is the first biosimilar.

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Alvotech and Teva Announce U.S. Approval of SIMLANDI®

SIMLANDI is the first citrate-free, high-concentration biosimilar to be designated interchangeable to Humira in the U.S.  SIMLANDI is the first biosimilar.

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