The purpose of this study is to evaluate the safety and tolerability of two dosing regimens of FG-3019 administered over 12 weeks in patients with diabetic nephropathy and proteinuria on background angiotensin converting enzyme inhibitor (ACEi) and/or angiotensin II receptor antagonist (ARB) therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
38
Unnamed facility
Birmingham, Alabama, United States
Unnamed facility
Tempe, Arizona, United States
Unnamed facility
La Mesa, California, United States
Safety and tolerability of FG-3019
Time frame: 34 weeks
Pharmacokinetic parameters
Time frame: 34 weeks
Change from baseline in first morning urinary albumin creatinine ratio (ACR)
Time frame: 6 weeks (10 mg/kg) or 10 weeks (5 mg/kg)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Torrance, California, United States
Unnamed facility
Kissimmee, Florida, United States
Unnamed facility
Atlanta, Georgia, United States
Unnamed facility
Springfield, Massachusetts, United States
Unnamed facility
Omaha, Nebraska, United States
Unnamed facility
Flushing, New York, United States
Unnamed facility
New York, New York, United States
...and 8 more locations