Madrid, 28007, Spain
NCT Number: NCT00195377
Study Evaluating Etanercept in Patients With Rheumatoid Arthritis(RA), Juvenile Idiopathic Arthritis (JIA), or Psoriatic Arthritis (PsA) in Spain
The purpose of this study is to assess the safety of etanercept in patients with rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA) or psoriatic arthritis (PsA) in Spain
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Notify MeKey information
Conditions
Age range
4 year and older
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
- RA or PsA in whom DMARDs/antiTNF antibodies/anti IL1 has been insufficient or inappropriate
- Children from 4 to 17 years old with JIA polyarticular
Exclusion criteria
- Clinically significant abnormal screening lab values
- Patients who are planning to undergo elective surgery during the study period.
- Other current autoimmune connective tissue diseases
Treatment and study plan
etanercept
DrugSponsors and collaborators
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
Evaluating Safety and QoL in Patients Treated With Etanercept: an Open Multicenter Study
Important dates
- Study start
- 2003
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Sep 19, 2005
- Registry last updated
- Jun 18, 2009
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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