FDA’s oncology advisory committee to consider MRD as a multiple myeloma endpoint

BY RACHEL COE, MSC

Yesterday, the FDA announced that its Oncologic Drugs Advisory Committee would weigh in on the potential use of minimal residual disease (MRD) as an endpoint in multiple myeloma clinical trials.

Cancers of the blood and bone marrow can affect production and function of white blood cells, red blood cells, and platelets, all produced by hematopoietic stem cells.

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