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Completed Phase 3 Interventional Results available

Study Utilizing Rilonacept in Gout Exacerbations

ClinicalTrials.gov ID: NCT00855920

Public ClinicalTrials.gov record NCT00855920. 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 Jul 22, 2026, 2:10 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 Multi-Center, Randomized, Double-Blind, Active-Controlled Study of the Safety and Efficacy of Rilonacept Administered Subcutaneously for the Treatment of an Acute Gout Flare

Study identification

NCT ID
NCT00855920
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
225 participants

Conditions and interventions

Interventions

  • Rilonacept Drug
  • Indomethacin Drug
  • Placebo (for Indomethacin) Other
  • Placebo (for Rilonacept) Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
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 28, 2009
Primary completion
Jan 31, 2010
Completion
Jan 31, 2010
Last update posted
Apr 27, 2017

2009 – 2010

United States locations

U.S. sites
44
U.S. states
19
U.S. cities
43
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Huntsville Alabama
Not listed Mesa Arizona
Not listed Phoenix Arizona
Not listed Sierra Vista Arizona
Not listed Burbank California
Not listed Whittier California
Not listed Clearwater Florida
Not listed DeBary Florida
Not listed DeLand Florida
Not listed Jupiter Florida
Not listed Orange Park Florida
Not listed Orlando Florida
Not listed Oviedo Florida
Not listed Boise Idaho
Not listed Elizabethtown Kentucky
Not listed Baltimore Maryland
Not listed Wheaton Maryland
Not listed Detroit Michigan 48221
Not listed Stevenville Michigan
Not listed Billings Montana
Not listed Albuquerque New Mexico
Not listed Albany New York
Not listed Burlington North Carolina
Not listed Cary North Carolina
Not listed Raleigh North Carolina 27612
Not listed Raleigh North Carolina
Not listed Wilmington North Carolina
Not listed Willoughby Hills Ohio
Not listed Oklahoma City Oklahoma
Not listed Lake Oswego Oregon
Not listed Portland Oregon
Not listed Johnstown Pennsylvania
Not listed Limerick Pennsylvania
Not listed Norristown Pennsylvania
Not listed Greenville South Carolina
Not listed Bristol Tennessee
Not listed Dallas Texas
Not listed Forth Worth Texas
Not listed Houston Texas
Not listed Irving Texas
Not listed Mesquite Texas
Not listed North Richland Hills Texas
Not listed San Antonio Texas

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00855920, 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 Apr 27, 2017 · Synced Jul 22, 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 NCT00855920 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →