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Clinical Trials · NCT05709444

A Phase IIb, Multicenter, Open-Label, Prospective Study of Bremelanotide in Diabetic Kidney Disease

CompletedPhase 2PT-141 (Approved)
Phase
Phase 2
Recruitment status
Completed
Sponsor
Palatin Technologies, Inc
Enrollment
16
Start date
Dec 2022
Locations
9 sites, United States
Primary endpoint
To demonstrate the efficacy of 0.5 mg subcutaneous BMT (given twice a day), used in combination with a subject's maximum tolerated dose of RAAS inhibition therapy, reduces urinary protein by 50% from baseline UP/Cr levels.
View PT-141 compound reference