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Clinical Trials · NCT06867835

Single Dose of Vyleesi in Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast Milk

CompletedPhase 4PT-141 (Approved)
Phase
Phase 4
Recruitment status
Completed
Sponsor
Cosette Pharmaceuticals, Inc.
Enrollment
10
Start date
Jul 2025
Locations
1 site, United States
Primary endpoint
Levels of Bremelanotide (BMT) in Breast Milk Over 24h After Administration of Vyleesi
View PT-141 compound reference