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Kraskovskaya N, Linkova N, Sakhenberg E, Krieger D, Polyakova V, Medvedev D, et al

BPC-157 requires robust safety trials in humans first, then trials to determine the dose-response required to elicit meaningful therapeutic regenerative changes, followed by trials to establish the long term safety

The choice between them in a research protocol typically depends on the cited prior literature being modelled tesamorelin has the larger HIV-lipodystrophy clinical-trial literature, CJC-1295 the larger non-HIV GH-axis preclinical literature