The purpose of this study is to evaluate the effect of treatment with CCX140-B on urinary albumin excretion in subjects with type 2 diabetes mellitus and albuminuria, as well as to study the safety and efficacy of the medication in this patient population.
Study acquired by Amgen and all disclosures were done by previous sponsor ChemoCentryx.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
20
Centre for Human Drug Research
Leiden, Netherlands
Change from baseline in 24-hour urinary albumin excretion
The primary efficacy objective of this study is to evaluate the effect of CCX140-B treatment on urinary albumin excretion by measuring change from baseline in 24-hour urinary albumin excretion.
Time frame: 84 days
Subject incidence of adverse events
The primary safety objective of this study is to evaluate the safety and tolerability of CCX140-B in subjects with type 2 diabetes mellitus (T2DM) with albuminuria.
Time frame: 84 days
Change from baseline in hemoglobin A1c
Time frame: 84 days
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