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Published in 2019 at "Blood"
DOI: 10.1182/blood-2019-123405
Abstract: Introduction: The intravenous (IV) formulation of human CD38 mAb DARA is approved in many countries as monotherapy or in combination with standard-of-care regimens for treatment of multiple myeloma (MM). To reduce patient (pt)/provider burden and…
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Keywords:
board directors;
dara;
membership entity;
janssen employment ... See more keywords