Christopher Hourigan, MD, DPhil, Virginia Tech FBRI Cancer Research Center, Washington, DC, outlines the uses of measurable residual disease (MRD) in acute myeloid leukemia (AML) and highlights its potential as a surrogate endpoint for accelerating regulatory approval in the drug development space. Dr Hourigan discusses some consortiums formed with this goal in mind. This interview took place at the Twelfth Annual Meeting of the Society of Hematologic Oncology (SOHO 2024) congress in Houston, TX.
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