Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

A Placebo Controlled Study to Assess Efficacy and Safety of Certolizumab Pegol in the Treatment of Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT00152386

Public ClinicalTrials.gov record NCT00152386. 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 Jun 25, 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 Phase III Multicentre, Double Blind, Placebo-controlled, Parallel Group 52-week Study to Assess the Efficacy and Safety of 2 Dose Regimens of Lyophilised CDP870 as Additional Medication to Methotrexate in the Treatment of Signs and Symptoms and Preventing Structural Damage in Patients With Active Rheumatoid Arthritis Who Have an Incomplete Response to Methotrexate

Study identification

NCT ID
NCT00152386
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
950 participants

Conditions and interventions

Interventions

  • Certolizumab pegol (CDP870) Drug

Drug

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
Jan 31, 2005
Primary completion
Sep 30, 2006
Completion
Sep 30, 2006
Last update posted
Nov 30, 2020

2005 – 2006

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Not listed Huntsville Alabama
Not listed Paradise Valley Arizona
Not listed La Jolla California
Not listed San Diego California
Not listed Denver Colorado
Not listed Danbury Connecticut
Not listed Washington D.C. District of Columbia
Not listed Aventura Florida
Not listed Ocala Florida
Not listed Orlando Florida
Not listed Sarasota 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 St Louis Missouri
Not listed Lincoln Nebraska
Not listed Charlotte North Carolina
Not listed Cleveland Ohio
Not listed Dayton Ohio
Not listed Duncansville Pennsylvania
Not listed Charleston South Carolina
Not listed Austin Texas
Not listed Dallas 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00152386, 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 Nov 30, 2020 · Synced Jun 25, 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 NCT00152386 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →