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Regarding pharmacodynamics, TZP appears as a biased GLP-1R-GIPR co-agonist, because of its positive effects on cAMP generation over -arrestin recruitment, which is conversely stimulated by GLP-1R
It is worth noting that these batteries use different C rates for various applications
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Calocurb's data represents apples-to-apples comparison because they're measuring actual hormone levels and appetite effects in similar populations, unlike typical comparisons where ingredients like berberine might increase GLP-1 by 65% -- enough for blood glucose management or statistical significance but not appetite suppression or clinical significance
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