Surrogate Endpoints Acceptable in AML Trials, Says FDA
In the case of drugs used for newly diagnosed acute myeloid leukemia (AML), surrogate endpoints have been validated, says the US Food and Drug Administration.
Medscape Medical News
source https://www.medscape.com/viewarticle/967529?src=rss
Medscape Medical News
source https://www.medscape.com/viewarticle/967529?src=rss
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