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The potency of samples following storage was then evaluated in the in vitro ROS assay in ARPE-19 cells as described above to evaluate impact of storage duration and additive on NAC oxidation

C.McCulloughS

I just want to make my final statement in the beginning statement of since Senator Vice Chair mentioned that we need to also address education aspect rather than just trying to treat mental health or behavioral health issues

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Clinical trial data from FDA-approved labeling typically report gastrointestinal adverse effects broadly, with nausea occurring in 1544% of patients depending on the specific agent and dose, while vomiting affects 524% of users