The purpose of this study is to evaluate the safety and efficacy of treatment with CCX140-B in subjects with diabetic nephropathy.
The primary objective of this study is to evaluate the safety and tolerability of CCX140-B in subjects with diabetic nephropathy based on subject incidence of adverse events. The secondary objectives of this study include evaluation of the effect of CCX140-B on several measures of effectiveness commonly used in the evaluation of diabetes and renal medications. Study acquired by Amgen and all disclosures were done by previous sponsor ChemoCentryx.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
332
Subject incidence of adverse events
The primary objective of this study is to evaluate the safety and tolerability of CCX140-B in subjects with diabetic nephropathy.
Time frame: Up to 365 days
Change from baseline in first morning urinary albumin:creatinine ratio (ACR)
Time frame: Up to 365 days
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Antwerp, Belgium
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Brussels, Belgium
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Edegem, Belgium
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Ghent, Belgium
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Leuven, Belgium
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Liège, Belgium
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Roeselare, Belgium
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Beroun, Czechia
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Brno, Czechia
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Hlučín, Czechia
...and 73 more locations