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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00440817
Other study ID # CR011239
Secondary ID C0168T68
Status Completed
Phase Phase 4
First received February 26, 2007
Last updated April 9, 2014
Start date February 2006
Est. completion date August 2006

Study information

Verified date April 2014
Source Centocor Ortho Biotech Services, L.L.C.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to examine the association with EBV infection, monitor the occurrence of lymphoma and assess lymphoma risk in patients with rheumatoid arthritis and/or Crohns disease and you have taken infliximab.


Description:

This is an observational (review of records), retrospective (research activity that is performed after the events under the study have occurred), registry study where data was collected from 3 different registries sponsored or supported by Centocor. Registries are Centocor-sponsored Therapy Resource Evaluation and Assessment Tool (TREATâ„¢) Registry of Crohn's Disease, and in the following two Centocor-supported registries the Consortium of Rheumatology Researchers of North America, Inc. (CORRONA) registry and the Infliximab RA Registry, a subset of the National Database Registry of Rheumatoid Arthritis (NDBRRA) and of the National Databank for Rheumatic Diseases (NDB). A registry is data collection in a real life physician-patient setting. Physicians prescribe medications for rheumatoid arthritis and/or Crohns disease in accordance with their usual clinical practice and then record this information and provide it to Centocor. For this registry study, Centocor collected data from 3 registries to evaluate the risk of getting lymphoma if you have rheumatoid arthritis and/or Crohns disease and you have taken infliximab. Patients who were in one of the 3 registries and had rheumatoid arthritis and/or Crohns disease and did not take infliximab were also evaluated. This registry study does not involve the use of any investigational drugs.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date August 2006
Est. primary completion date August 2006
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with Crohns disease or rheumatoid arthritis who participate in the specified registries will be included in the analysis. For the lymphoma analysis, patients must be recorded as having a lymphoma during their participation in one of these registries

Exclusion Criteria:

- Patients who do not have Crohns disease or rheumatoid arthritis and who did not participate in one of the identified registries will be excluded from the study

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Other:
No intervention
All treatments are prescribed by a physician on the basis of usual clinical practice.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centocor Ortho Biotech Services, L.L.C.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Occurrence of lymphoma To examine the occurrence of lymphoma among patients in one Centocor-sponsored and Centocor-supported disease registries 5 years No
Secondary Assessment of lymphoma risk To assess lymphoma risk in relevant registry patient populations, including patients not receiving anti-TNF therapies, patients receiving conventional immunosuppressants (including corticosteroids), and patients receiving anti-TNF therapies 5 years No
Secondary Evaluation of association of Epstein-Barr Virus (EBV) with the lymphoma To evaluate all available data on tissue samples of individual lymphoma cases for the potential association of EBV with the lymphoma. 5 years No
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