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Thus, while each platform has demonstrated proof-of-concept efficacy, the choice of design must balance responsiveness, stability, and biosafety to ensure clinical applicability

9 In the United States, the Department of Defenses Operation Supplement Safety and the FDA have flagged BPC-157 as an unapproved drug with unresolved concerns about impurities and immunogenicity when sold in injectable research products, and it has been the subject of ongoing compounding-eligibility review rather than approval

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Results: Over the 11-year study period, 405 LT for SLD were performed at our center: 126 (31%) ALD, 114 (28%) AH, 137 (34%) MASLD, and 28 (7%) MetALD

Stefan Wagner, and Dr