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However, dose escalation must be balanced against tolerability and side effects

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

Protecting bone health is a critical aspect of the treatment plan, and it helps to have a way to measure muscle mass and bone health, like a BIA body composition device or a Hume Health Body Pod device that can assess bone health