A Study to Evaluate Safety of Long Term Therapy of Certolizumab Pegol Patients With Crohn's Disease
Public ClinicalTrials.gov record NCT00552344. 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.
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, Multinational, Open-label, follow-on Trial to C87085 Designed to Assess the Long-term Safety of Certolizumab Pegol, a Pegylated Fab' Fragment of a Humanized Anti-TNF-alpha Monoclonal Antibody, Administered at Weeks 0, 2 and 4, and Then Every 4 Weeks Thereafter, in Subjects With Moderately to Severely Active Crohn's Disease Who Have Participated in Study C87085
Study identification
- NCT ID
- NCT00552344
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- UCB BIOSCIENCES GmbH
- Industry
- Enrollment
- 403 participants
Conditions and interventions
Conditions
Interventions
- Cimzia Biological
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
- Apr 30, 2008
- Primary completion
- Nov 30, 2014
- Completion
- Nov 30, 2014
- Last update posted
- Aug 8, 2018
2008 – 2014
United States locations
- U.S. sites
- 20
- U.S. states
- 14
- U.S. cities
- 19
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| 284 | Lakewood | Colorado | — | — |
| 285 | Littleton | Colorado | — | — |
| 278 | New Port Richey | Florida | — | — |
| 300 | Winter Park | Florida | — | — |
| 276 | Chicago | Illinois | — | — |
| 279 | Louisville | Kentucky | — | — |
| 275 | Metairie | Louisiana | — | — |
| 307 | Monroe | Louisiana | — | — |
| 281 | Annapolis | Maryland | — | — |
| 295 | Towson | Maryland | — | — |
| 310 | Chesterfield | Michigan | — | — |
| 298 | Rochester | Minnesota | — | — |
| 272 | Raleigh | North Carolina | — | — |
| 296 | Cincinnati | Ohio | — | — |
| 289 | Cleveland | Ohio | — | — |
| 280 | Lancaster | Pennsylvania | — | — |
| 305 | Germantown | Tennessee | — | — |
| 306 | Germantown | Tennessee | — | — |
| 308 | Norfolk | Virginia | — | — |
| 290 | 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 80 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00552344, 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 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 NCT00552344 live on ClinicalTrials.gov.