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Clinical Trial Summary

This is a prospective, open-label trial to assess the efficacy of melanocortin receptor agonist bremelanotide (BMT) when administered with RAAS inhibition therapy after six months in subjects with Type II diabetic nephropathy. After six months of therapy, all subjects will remain in trial for further assessment and undergo a diagnostic renal biopsy to assess the effect of melanocortin therapy on diabetic histopathology at 12 months.


Clinical Trial Description

A total of 45 subjects with biopsy-proven Type II diabetic nephropathy and >1000 mg/gm UP/Cr ratio will be enrolled to receive BMT therapy in addition to their maximum tolerated RAAS inhibition therapy for six months. The subjects' historical medical and laboratory data collected at four timepoints, approximately 18, 12, and 6 months prior to Day 0, will be reviewed and recorded to be used as baseline values. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05709444
Study type Interventional
Source Palatin Technologies, Inc
Contact Brian Dodge
Phone 640-203-9743
Email bdodge@palatin.com
Status Recruiting
Phase Phase 2
Start date December 26, 2022
Completion date February 5, 2024

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