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Healthcare providers typically rely on clinical evaluation, a detailed medical history, and the presence of symptoms following exposure to GBCAs

Tofacitinib in steroid-refractory acute severe ulcerative colitis: a retrospective analysis

The feasibility of many transplant and trauma procedures is limited by the time required to transport donor tissues to the recipient (Totsuka et al

Producing a novel triple-agonist peptide at commercial scale requires specialized facilities and processes

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