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Completed Phase 3 Interventional Results available

A Study of the Safety and Efficacy of Infliximab(REMICADE ) in Pediatric Patients With Moderately to SeverelyActive Ulcerative Colitis

ClinicalTrials.gov ID: NCT00336492

Public ClinicalTrials.gov record NCT00336492. 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 22, 2026, 6:01 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 3, Randomized, Open-label, Parallel-group, Multicenter Trial to Evaluate the Safety and Efficacy of Infliximab (REMICADE�) in Pediatric Subjects With Moderately to Severely Active Ulcerative Colitis

Brief summary

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

The purpose of the study is to evaluate the effectiveness and safety of infliximab (Remicade) in children with moderately to severely active ulcerative colitis.

Study identification

NCT ID
NCT00336492
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Centocor, Inc.
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

Biological

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
Sep 2006 (Type not available)
Primary completion
May 2009 (Actual)
Completion
Apr 2010 (Actual)
Last update posted
Jul 30, 2013

2006 – 2010

United States locations

U.S. sites
18
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Phoenix Arizona — —
Not listed Los Angeles California — —
Not listed Denver Colorado — —
Not listed Hartford Connecticut — —
Not listed Orlando Florida — —
Not listed Atlanta Georgia — —
Not listed Chicago Illinois — —
Not listed Indianapolis Indiana — —
Not listed Boston Massachusetts — —
Not listed Rochester Minnesota — —
Not listed New Hyde Park New York — —
Not listed Durham North Carolina — —
Not listed Cleveland Ohio — —
Not listed Columbus Ohio — —
Not listed Dayton Ohio — —
Not listed Providence Rhode Island — —
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 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00336492, 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 Jul 30, 2013 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00336492 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →