Apr 23, 2024 · An FDA committee voted 12-0 in favor of using minimal residual disease negativity as an early outcome measure in trials of multiple myeloma.
Apr 12, 2024 · ... minimal residual disease (MRD) testing as an early endpoint for the accelerated approval of multiple myeloma drugs in clinical trials. ODAC ...
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Apr 12, 2024 · ... (12-0) of using minimal residual disease (MRD) as an early endpoint for accelerated approval in multiple myeloma clinical trials. This means ...
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Apr 18, 2024 · For this advisory meeting, the FDA convened the ODAC “to discuss the adequacy of available data to support the use of minimal residual disease ( ...
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Apr 12, 2024 · The FDA's ODAC voted that data support the use of minimal residual disease as an end point to support accelerated approval of treatments in ...
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Apr 12, 2024 · The Oncologic Drugs Advisory Committee determined that minimal residual disease could serve as an accelerated approval end point in multiple ...
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Mar 26, 2024 · The Committee will discuss the use of minimal residual disease (MRD) as an endpoint in multiple myeloma clinical trials, including ...
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Apr 29, 2024 · The Oncologic Drugs Advisory Committee unanimously voted in agreement that minimal residual disease is a reasonable endpoint for accelerated ...
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Apr 15, 2024 · The FDA ODAC Committee makes a historic 12-0 vote to approve Minimal Residual Disease (MRD) as a new clinical trial endpoint in multiple myeloma
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