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Phase I human trial of parent molecule (TB-4) showed no serious adverse events Mild injection site reactions possible Same theoretical angiogenesis/tumor concern as BPC-157 Head rush or lightheadedness reported anecdotally at higher doses Can You Stack BPC-157 and TB-500

Subcutaneous injection provides higher bioavailability (approximately 80-90%) compared to oral administration (15-20%)

The completion of a Phase I trial is a significant milestone, as its primary objective is to assess safety and tolerability in human subjects