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Claytons research contributions to PT-141 development include: Principal investigator for pivotal Phase 2 dose-finding trial establishing optimal 1.75 mg dose Lead investigator for RECONNECT Phase 3 trials supporting FDA approval Development of responder analysis methodology for patient-reported outcomes in sexual dysfunction Neurobehavioral research elucidating central mechanisms of sexual desire Extensive publication record on bremelanotide efficacy, safety, and clinical applications Her work has established PT-141 as the second FDA-approved pharmacological treatment for HSDD and the first melanocortin-based therapy for sexual dysfunction, representing a significant advance in womens sexual health treatment options

HDLs are heterogeneous density lipoproteins with varying size and composition

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Impact of cell-surface antigen expression on target engagement and function of an epidermal growth factor receptor c-MET bispecific antibody

In particular, standard 1D proton spectra and 2D experiments (clean total-correlation spectroscopy (TOCSY) and heteronuclear single quantum coherence (HSQC)) were acquired providing one-dimensional metabolic profiles and homonuclear and heteronuclear spectra for metabolite identification