Upstate Active Clinical Trials
Study Title:A Randomized, Double Blind, Placebo controlled, dose assessment phase II study to
evaluate the safety and efficacy of CCX168 in subjects with anti-neutrophil cytoplasmic antibody (ANCAAssociated
What is the purpose of the study?The main safety objective of this study is to evaluate the safety and tolerability of CCX168 when it is given to patients who are receiving the standard therapy for AAV.
This study will also assess the efficacy of the treatment with CCX168 in combination with the standard therapy in the treatment of AAV.
This study will also evaluate if CCX168 improves your symptoms, your kidney function (if you have kidney disease involvement) and your overall disease activity when compared to the treatment with placebo (“sugar pills”)
Upstate Institutional Review Board (IRB) Number:732499
Study/Protocol ID:Protocol CL003_168
Study Phase:Phase II
Patient Age Group:Adults
Principal Investigator:Sriram S Narsipur
Who can I contact for more information?
Name: Linda L Spillett, CCRP