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Completed Phase 4 Interventional Results available

Dosing Flexibility Study in Patients With Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT00580840

Public ClinicalTrials.gov record NCT00580840. 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 Oct 21, 2026, 7:32 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 IIIb Open-label run-in Double-blind, Placebo Controlled, Randomized Study to Evaluate the Safety/Efficacy of Certolizumab Pegol Administered Concomitantly With Stable-dose Methotrexate in Patients With Active Rheumatoid Arthritis.

Brief summary

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

During the run-in period, CZP will be administered at 400 mg (2 injections) at Wks 0, 2, and 4 and 200 mg with placebo (1 injection placebo, 1 injection CZP) at Wks 6, 8, 10, 12, 14 and 16. At Wk 18 patients will be grouped as responders or non-responders based on results of the ACR20 at Week 16.

Study identification

NCT ID
NCT00580840
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
UCB Pharma
Industry
Enrollment
333 participants

Conditions and interventions

Interventions

Drug · Other

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
Dec 2007 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Mar 2011 (Actual)
Last update posted
Aug 2, 2018

2007 – 2011

United States locations

U.S. sites
50
U.S. states
23
U.S. cities
50
Facility City State ZIP Site status
Not listed Huntsville Alabama — —
Not listed Montgomery Alabama — —
Not listed Gilbert Arizona — —
Not listed Paradise Valley Arizona — —
Not listed Tucson Arizona — —
Not listed Little Rock Arkansas — —
Not listed Huntington Beach California — —
Not listed La Jolla California — —
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Not listed Palm Desert California — —
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Not listed San Diego California — —
Not listed Colorado Springs Colorado — —
Not listed Aventura Florida — —
Not listed Clearwater Florida — —
Not listed Gainesville Florida — —
Not listed Jacksonville Florida — —
Not listed Jupiter Florida — —
Not listed Melbourne Florida — —
Not listed Sarasota Florida — —
Not listed Bogart Georgia — —
Not listed Morton Grove Illinois — —
Not listed Vernon Hills Illinois — —
Not listed Lexington Kentucky — —
Not listed Portland Maine — —
Not listed Haverhill Massachusetts — —
Not listed Pittsfield Massachusetts — —
Not listed Worcester Massachusetts — —
Not listed Rochester Minnesota — —
Not listed Kansas City Missouri — —
Not listed Lincoln Nebraska — —
Not listed Las Vegas Nevada — —
Not listed Reno Nevada — —
Not listed Albany New York — —
Not listed Mineola New York — —
Not listed Syracuse New York — —
Not listed Charlotte North Carolina — —
Not listed Monroe North Carolina — —
Not listed Wilmington North Carolina — —
Not listed Cleveland Ohio — —
Not listed Perrysburg Ohio — —
Not listed Norman Oklahoma — —
Not listed Oklahoma City Oklahoma — —
Not listed Duncansville Pennsylvania — —
Not listed Simpsonville South Carolina — —
Not listed Dallas Texas — —
Not listed San Antonio Texas — —
Not listed Sugar Land Texas — —
Not listed Tyler Texas — —
Not listed Vancouver 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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00580840, 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 Aug 2, 2018 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00580840 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →