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doi: 10.1021/acs.chemrestox.9b00152 164 AltomareABaronGBrioschiMLongoniMButtiRValvassoriEet al

The field requires urgent Phase I/II human trials before any clinical recommendations can be made

PubMed Schiavon R, Freeman GE, Guidi GC, et al

Bremelanotide has gone through the entire pharmaceutical development process: it underwent Phase III clinical trials and was approved as a drug in the United States for a specific indication of hypoactive sexual desire disorder in women, under the brand name Vyleesi

A healthcare provider can assess individual risk factors and recommend appropriate dosing strategies

To further improve skin permeation compared to native GFs, the complex was incorporated into cationic elastic liposomes (ELs)