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Clinical Trial Summary

The primary safety objective of this study is to evaluate the safety and tolerability of CCX168 in subjects with IgAN on background supportive therapy with a maximally tolerated dose of RAAS blockade. The primary efficacy objective is to evaluate the efficacy of CCX168 based on an improvement in proteinuria.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02384317
Study type Interventional
Source ChemoCentryx
Contact
Status Completed
Phase Phase 2
Start date March 27, 2015
Completion date June 1, 2018

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