Metro Manila, Philippines
NCT Number: NCT00683384
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.
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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.
Treatment and study plan
Etanercept (Enbrel)
DrugPrimary outcomes
-
Number of Participants With Spontaneous Adverse Events Reported Until 30 Days After Each Injection
Time frame: 30 days post injection up to 3 years
Sponsors and collaborators
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
A Prospective, Observational Study to Monitor Safety in Patients Who Were Administered With Etanercept (Enbrel) 25 mg by Subcutaneous Injection
Important dates
- Study start
- 2007
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- May 23, 2008
- Registry last updated
- Nov 16, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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