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Completed Phase 3 Interventional Results available

Open Label Long-Term Safety Study of Certolizumab Pegol (CZP) for Patients With Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT00160693

Public ClinicalTrials.gov record NCT00160693. 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 24, 2026, 10:23 AM 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 Phase III, Multicenter, Open-Label Long-Term Study to Assess the Safety and Tolerability of CDP870 400 mg Subcutaneously Every 4 Weeks, in Subjects With Rheumatoid Arthritis

Study identification

NCT ID
NCT00160693
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
402 participants

Conditions and interventions

Interventions

  • Certolizumab Pegol Biological

Biological

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 28, 2003
Primary completion
Jan 31, 2011
Completion
Jan 31, 2011
Last update posted
Jul 31, 2018

2003 – 2011

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
29
Facility City State ZIP Site status
Not listed Huntsville Alabama
Not listed Paradise Valley Arizona
Not listed Washington D.C. District of Columbia
Not listed Aventura Florida
Not listed Clearwater Florida
Not listed Ocala Florida
Not listed Orlando Florida
Not listed Tampa Florida
Not listed Coeur d'Alene Idaho
Not listed Springfield Illinois
Not listed Wichita Kansas
Not listed Wheaton Maryland
Not listed Fall River Massachusetts
Not listed St Louis Missouri
Not listed Lincoln Nebraska
Not listed Charlotte North Carolina
Not listed Cleveland Ohio
Not listed Dayton Ohio
Not listed Erie Pennsylvania
Not listed West Reading Pennsylvania
Not listed Charleston South Carolina
Not listed Memphis Tennessee
Not listed Austin Texas
Not listed Dallas Texas
Not listed Duncanville Texas
Not listed Lubbock Texas
Not listed San Antonio Texas
Not listed San Diego Texas
Not listed Everett 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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00160693, 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 Jul 31, 2018 · Synced Jul 24, 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 NCT00160693 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →