Has Minimal Residual Disease (MRD) testing been approved by the FDA yet? (https://www.myeloma.org/videos/has-minimal-residual-disease-mrd-testing-been-approved-fda-yet)
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In this week’s video, Dr. Brian G.M. Durie explains that the FDA will soon consider MRD-testing as a surrogate endpoint for both newly diagnosed and relapsed myeloma patients. BOTTOM LINE: |
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If you have a question that you’d like to suggest for a future episode of Ask Dr. Durie, please submit it to [email protected] (mailto:[email protected]). To reach the IMF InfoLine Coordinators, please call 800.452.2873 or email them at [email protected] (mailto:[email protected]). |
Dr. Brian G.M. Durie serves as Chairman of the International Myeloma Foundation and serves on its Scientific Advisory Board. Additionally, he is Chairman of the IMF's International Myeloma Working Group, a consortium of nearly 200 myeloma experts from around the world. Dr. Durie also leads the IMF’s Black Swan Research Initiative®.