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Completed No phase listed Observational

A Long-term Safety Study of Infliximab in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD).

ClinicalTrials.gov ID: NCT00380796

Public ClinicalTrials.gov record NCT00380796. 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 Nov 11, 2026, 7:55 PM EST

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Official title

A Multicenter, Observational Study of the Long-term Safety of Infliximab (REMICADE) in Subjects With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD). RESULTS COPD: REMICADE Safety Under Long Term Study in COPD

Brief summary

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

The purpose of this long-term observational study is designed to collect additional information on incidence of cancer and cause of death among patients who have participated in clinical trials of infliximab in the treatment of COPD. Patients must have received at least 1 dose of study agent (ie, placebo or infliximab) in the primary studies to be eligible for participation in this long-term follow-up study. Information on deaths and cancers will be collected twice yearly for a period of 5 years from each patient's last safety visit in the primary study.

Study identification

NCT ID
NCT00380796
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Centocor, Inc.
Industry
Enrollment
88 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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 2006 (Type not available)
Primary completion
Dec 2009 (Actual)
Completion
Dec 2009 (Actual)
Last update posted
Sep 4, 2013

2006 – 2009

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Not listed Anaheim California — —
Not listed San Diego California — —
Not listed Bay Pines Florida — —
Not listed Clearwater Florida — —
Not listed Blue Ridge Georgia — —
Not listed Baltimore Maryland — —
Not listed Springfield Massachusetts — —
Not listed Minneapolis Minnesota — —
Not listed Saint Charles Missouri — —
Not listed St Louis Missouri — —
Not listed Omaha Nebraska — —
Not listed Las Vegas Nevada — —
Not listed Lebanon New Hampshire — —
Not listed Endwell New York — —
Not listed Larchmont New York — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Easton Pennsylvania — —
Not listed Hershey Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Greer South Carolina — —
Not listed Spartanburg South Carolina — —
Not listed Amarillo Texas — —
Not listed Dallas Texas — —
Not listed Salem Virginia — —
Not listed Madison Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00380796, 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 Sep 4, 2013 · Synced Nov 11, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00380796 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →