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PT-141 has undergone full Phase 3 clinical trials with over 1,200 subjects and received FDA approval as bremelanotide (Vyleesi) for female hypoactive sexual desire disorder in 2019, which means it has passed formal safety and efficacy review

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Furthermore, the TRT group exhibited significant reductions in key liver parameters by the conclusion of the trial

Review and download COA details on the product page before incorporating material into regulated studies

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