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Journal of Controlled Release, 336 , 310-321
Additionally, there were very few clinically associated studies, where many of the articles available consisted of literature and narrative reviews or non-evidence-based guidelines based on literature searches with limited methods reported
PT-141 was FDA-approved in 2019 under the brand name Vyleesi for the treatment of hypoactive sexual desire disorder (HSDD) in premenopausal women, representing the first melanocortin receptor agonist approved for this indication
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