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Study Evaluating the Safety of Enbrel (Etanercept) | Clinical Trials | Clareo Health

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COMPLETEDNCT00683384

Study Evaluating the Safety of Enbrel (Etanercept)

The purpose of this study is to collect post-marketing information on the safety of Enbrel in Filipino patients.

Lead sponsor: Wyeth is now a wholly owned subsidiary of Pfizer•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Wyeth is now a wholly owned subsidiary of Pfizer

Age

All ages

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•All patients from the study center who received or will receive at least one dose of Enbrel according to the approved product indication.

Exclusion Criteria

•Previously discontinued Enbrel therapy due to significant safety concern.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: November 16, 2010Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment93

Start dateJan 2007

Last updatedNov 16, 2010

Condition

Arthritis, Psoriatic

Locations shown

Metro Manila

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 16, 2010Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions