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Medical approval: In 2019, the FDA approved PT-141 under the trade name Vyleesi for treating hypoactive sexual desire disorder (HSDD) in premenopausal women

10.1038/78829 116 SprustonN.JonasP.SakmannB

Moreover, a randomized, evaluator-blinded clinical trial including 40 Brazilian women with facial melasma who underwent broad-spectrum tinted sunscreen and nightly application of 5% cysteamine or 4% HQ for 16 weeks resulted in an MASI reduction of 32% and 52%, respectively [31]