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Targeting refractory sarcomas and malignant peripheral nerve sheath tumors in a phase I/II study of sirolimus in combination with Ganetespib (SARC023)
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PT-141 became the active compound in Vyleesi (bremelanotide injection), FDA-approved in 2019 for hypoactive sexual desire disorder (HSDD) in premenopausal women one of the few research peptides to achieve full FDA approval, providing a clinically validated pharmacological profile
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