A Randomized, Double-Blind, Placebo Controlled, Dose Assessment Phase 2 Study to Evaluate the Safetyand Efficacy of CCX168 in Subjects with Anti-Neutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis
A study for subjects with Vasculitis using study drug CCX168 for treatment
Sponsor: ChemoCentryx
Enrolling: Male and Female Patients
IRB Number: AAAO0256
U.S. Govt. ID: NCT02222155
Contact: Irma Orbe: 212-342-0838 / io67@columbia.edu
Additional Study Information: The purpose of this study is to evaluate the safety and tolerability of study drug CCX168 when it is given to patients who are receiving the standard therapy for a certain type of vasculitis called ANCA-associated vasculitis (AAV). The study will also assess the effectiveness of the study drug, CCX168, in combination with the standard treatment of AAV. This study will also evaluate if CCX168 improves patients' symptoms, their kidney function (if they have kidney disease involvement) and their overall disease activity when compared to placebo (sugar pills) while they continue the standard treatment with cyclophosphamide or rituximab and prednisone.
This study is closed
Investigator
Andrew Bomback, MD
Do You Qualify?
Do you have any other multi-system autoimmune disease? Yes No
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Place Holder




For more information, please contact:
Irma Orbe
io67@columbia.edu
212-342-0838