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A Phase 2 trial (NCT01311518) was designed to test RGN-352 in ~75 heart attack patients, but was placed on FDA clinical hold in 2011 due to manufacturing (GMP) compliance issues at the contract site not safety concerns with the drug itself

Readers should use the section to check current eligibility, pharmacy or provider policies, and safety questions with a licensed professional before acting

Researchers conducting in vitro or cell-based assays in particular should confirm low endotoxin levels in any BPC-157 peptide preparation before use, as cellular assay systems are particularly sensitive to lipopolysaccharide contamination artifacts