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When a compound has no completed human trial, there is by definition no safety data in any subgroup no pregnancy data, no hepatic-impairment data, no interaction data with common metabolic or endocrine medications
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Careful explanation was sufficient reassurance that there would be no untoward effects
The only way to waste that advantage is by introducing protocol inconsistency (missed doses, erratic intervals) or handling errors (contamination, temperature abuse) that timing optimization can't fix
For example, she said, the FDA committee is evaluating BPC-157 specifically for ulcerative colitis, but wellness clinics may say simply that BPC-157 is approved, implying that it is approved for everything
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