ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Study to Evaluate Efficacy and Safety of Certolizumab Pegol for Induction of Remission in Patients With Crohn's Disease

ClinicalTrials.gov ID: NCT00552058

Public ClinicalTrials.gov record NCT00552058. 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 May 12, 2026, 10:08 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

Phase IIIb, Multinational, Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of Certolizumab Pegol, a Pegylated Fab' Fragment of a Humanized Anti-Tumor Necrosis Factor(TNF)-Alpha Monoclonal Antibody, Administered in Subjects With Moderately to Severely Active Crohn's Disease.

Study identification

NCT ID
NCT00552058
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
439 participants

Conditions and interventions

Conditions

Interventions

  • Placebo Other
  • certolizumab pegol (CDP870, CZP) Biological

Other · Biological

Eligibility (public fields only)

Age range
18 Years to 75 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 29, 2008
Primary completion
Sep 30, 2009
Completion
Oct 31, 2009
Last update posted
Aug 8, 2018

2008 – 2009

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Not listed Pell City Alabama
Not listed Colorado Springs Colorado
Not listed Lakewood Colorado
Not listed Littleton Colorado
Not listed Hollywood Florida
Not listed Jacksonville Florida
Not listed New Port Richey Florida
Not listed Winter Park Florida
Not listed Chicago Illinois
Not listed Louisville Kentucky
Not listed Metairie Louisiana
Not listed Monroe Louisiana
Not listed Annapolis Maryland
Not listed Towson Maryland
Not listed Chesterfield Michigan
Not listed West Bloomfield Michigan
Not listed Rochester Minnesota
Not listed Raleigh North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Lancaster Pennsylvania
Not listed Germantown Tennessee
Not listed Norfolk Virginia
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 92 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00552058, 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 8, 2018 · Synced May 12, 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 NCT00552058 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →