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GEP12 was designed to incorporate findings published by Jones, Buenaventura et al
However, the lack of FDA approval and oversight for the final compounded products introduces inherent risks. Douglas Ewing, MD, FACS, DABOM Concerns have been raised about the potential for contamination, impurities, and incorrect dosages in some compounded products, Ewing continued
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Features Aib8 substitution for DPP-4 resistance
In comparison, researchers who administer peptide injections will receive their peptides in the form of lyophilized powder, which must be reconstituted with a sterile solvent like bacteriostatic water
Zamani M, et al
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