An ambulatory blood pressure monitoring study of three bremelanotide doses (0.75, 1.25, 1.75 mg) in 397 premenopausal women. Bremelanotide produced small, transient blood pressure increases (peaked at 0–4 hours) that resolved within 12 hours. The 1.75 mg approved dose's BP effect was considered clinically acceptable, informing the FDA approval and post-marketing cardiovascular monitoring guidance.
White, William B; Myers, Martin G; Jordan, Robert; Lucas, Johna