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No serious adverse events, liver enzyme elevations, or cardiovascular changes were documented in the Phase 1 safety study published in the Journal of Clinical Endocrinology & Metabolism in 2024
& Sorrentino, C
Thus, the number of participants are lower than the number who completed the clinical trials in most cases since blood was not always obtained from every participant at the end of the trial for various reasons, including the participant refusal
The argument made by some vendors was that because PDA uses an arginine counterion rather than acetate, it constitutes a distinct chemical entity not covered by the BPC-157 Category 2 ruling
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