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Completed Phase 2 Interventional Results available

Clinical Trial to Evaluate Safety and Efficacy of CCX168 in ANCA-Associated Vasculitis

ClinicalTrials.gov ID: NCT02222155

Public ClinicalTrials.gov record NCT02222155. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 6:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Dose Assessment Phase 2 Study to Evaluate the Safety and Efficacy of CCX168 in Subjects With Anti-Neutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The aim of this trial is to test the safety and efficacy of two dose regimens of the complement C5a receptor CCX168 in patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). Funding Source - FDA OOPD

Study identification

NCT ID
NCT02222155
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Amgen
Industry
Enrollment
42 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 3, 2015
Primary completion
Apr 23, 2016
Completion
Jul 18, 2016
Last update posted
Mar 12, 2025

2015 – 2016

United States locations

U.S. sites
39
U.S. states
27
U.S. cities
39
Facility City State ZIP Site status
Not listed Huntsville Alabama
Not listed Phoenix Arizona
Not listed Tucson Arizona
Not listed Long Beach California
Not listed Los Angeles California
Not listed San Francisco California
Not listed Aurora Colorado
Not listed Washington D.C. District of Columbia
Not listed Miami Springs Florida
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Kansas City Kansas
Not listed Lexington Kentucky
Not listed Louisville Kentucky
Not listed Shreveport Louisiana
Not listed Charlestown Massachusetts
Not listed Duluth Minnesota
Not listed Tupelo Mississippi
Not listed St Louis Missouri
Not listed Reno Nevada
Not listed Lebanon New Hampshire
Not listed Albuquerque New Mexico
Not listed Great Neck New York
Not listed Mineola New York
Not listed New York New York
Not listed Syracuse New York
Not listed Chapel Hill North Carolina
Not listed New Bern North Carolina
Not listed Columbus Ohio
Not listed Duncansville Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Providence Rhode Island
Not listed Charleston South Carolina
Not listed Chattanooga Tennessee
Not listed Amarillo Texas
Not listed Austin Texas
Not listed Houston Texas
Not listed Salt Lake City Utah
Not listed Seattle Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02222155, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 12, 2025 · Synced Sep 3, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02222155 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →