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Third, these new results show convincingly that major adverse CV events benefits are independent of the structural basis of the GLP-1 receptor analogue, assuaging concerns that exendin-4-based agonists are less effective than human GLP-1-based molecules.

PubMed Duley, L., Gulmezoglu, A

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Discovery of DS68702229 as a potent, orally available NAMPT (nicotinamide phosphoribosyltransferase) activator

BPC-157 adds a tissue repair dimension

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