FDA adcom backs MRD as new endpoint in multiple myeloma trials

By a unanimous 12-0 vote, the U.S. FDA’s Oncologic Drugs Advisory Committee concluded that new evidence support the use of minimal residual disease (MRD) as an accelerated approval endpoint in multiple myeloma (MM) clinical trials.

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,Oncologic Drugs Advisory Committee ,Drugs Advisory Committee ,Bioworld ,Multiple Myeloma ,Hodac ,Minimal Residual Disease ,Regulatory ,Cancer ,Us ,Fda ,Endpoint ,