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BPC-157 is not FDA-approved for any therapeutic use

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Preclinical investigations encompassing ethanol-induced gastric mucosal lesions, NSAID-mediated ulceration, cysteamine-induced duodenal injury, and inflammatory bowel disease analogues have reported associations between BPC157 exposure and reductions in mucosal lesion surface area, preservation of submucosal vascular architecture, and modulation of mucosal structural integrity

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Since the binding of testosterone to the AR is what actually causes the effects typically associated with testosterone (i.e

22 (5), e36e38 (2011)