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doi: 10.1016/j.jacl.2012.03.003

Hels et al

Using this approach to pharmacokinetic modeling, which appropriately captured our experimental pharmacokinetic data in rats (Figure 7B, Table S7), enabled us to characterize the release kinetics of the GLP-1 RA drugs from our hydrogel depot in vivo

In the low-glucose (0.1 mM) state, DCA-stimulated GLP-1 secretion was completely inhibited by 1-M pasireotide treatment, paralleling the cAMP levels in GLUTag cells (Fig

According to the FDA Adverse Event Reporting System (FAERS), the agency has received more than 8,500 reports of gastrointestinal issues from patients who take these medications
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Who Is This Approach Relevant For