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Terminated Phase 2 Interventional Results available

The Use of Certolizumab Pegol for Treatment of Active Crohn's Disease in Children and Adolescents

ClinicalTrials.gov ID: NCT00899678

Public ClinicalTrials.gov record NCT00899678. 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 Sep 24, 2026, 8:18 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 2, Open-label, Multicenter Study to Assess the Safety and Efficacy of Certolizumab Pegol in Children and Adolescents With Active Crohn's Disease (NURTURE Study)

Brief summary

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

The purpose of this study is to evaluate the safety, efficacy, pharmacokinetics, and immunogenicity of certolizumab pegol treatment in pediatric subjects, aged 6 to 17, with moderately to severely active Crohn's disease. The target enrollment is 160 subjects.

Study identification

NCT ID
NCT00899678
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Celltech
Industry
Enrollment
99 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Years to 17 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
Mar 31, 2009
Primary completion
Jun 30, 2012
Completion
Jun 30, 2012
Last update posted
Aug 6, 2018

2009 – 2012

United States locations

U.S. sites
24
U.S. states
21
U.S. cities
24
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Los Angeles California — —
Not listed Orange California — —
Not listed San Francisco California — —
Not listed Aurora Colorado — —
Not listed Hartford Connecticut — —
Not listed Orlando Florida — —
Not listed Atlanta Georgia — —
Not listed Chicago Illinois — —
Not listed Indianapolis Indiana — —
Not listed Lexington Kentucky — —
Not listed Shreveport Louisiana — —
Not listed Baltimore Maryland — —
Not listed Boston Massachusetts — —
Not listed Rochester Minnesota — —
Not listed Morristown New Jersey — —
Not listed New Hyde Park New York — —
Not listed Cincinnati Ohio — —
Not listed Philadelphia Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed Seattle Washington — —
Not listed Milwaukee Wisconsin — —

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00899678, 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 6, 2018 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00899678 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →