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Sadri responded to FDA's Form 483 to explain the discrepancies, including delayed activation of the clinical trial site and shortening of the enrollment period, and said he would update the standard operating procedures
doi: 10.1016/j.biopha.2016.12.056
P.MifflinL.ZouC.et al
8 Kinetic and mutagenesis study of GPX4 degradation mechanism after treatment with ferroptosis inducers
