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For standard oral solid dosage forms, the primary endpoint is pharmacokinetic: the 90% confidence interval for the ratio of AUC and Cmax between generic and RLD must fall within 80125%

PMID: 67 YassineFNajmABilenM

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Key highlights from the announcement: In the trial, participants with #obesity or #overweight achieved .% , with benefits extending to cardiometabolic risk factors such as blood pressure and systemic inflammation

Next, the cell medium was replaced, and 100 L of different doses of AP probe-net (final concentration: 100, 75, 50, 25, 12.5, 6.25, 3.12 and 1.56 M) were added and incubated for another 24 h and 48 h, respectively