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An Open-label Extension Study of CACZ885H2357E1 on the Treatment and Prevention of Gout Flares in Patients With Frequent Flares for Whom NSAIDs and/ or Colchicine Are Contraindicated, Not Tolerated or Ineffective

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City:   Newport News
State:   Virginia
Zip Code:   23606
Conditions:   Acute Gout
Purpose:   The purpose of this second extension study is to collect long-term safety and tolerability data and additional efficacy data in patients who are treated on demand upon flare with canakinumab.
Study Summary:  
Criteria:   Inclusion Criteria: Patients who have either: - Completed the first extension study CACZ885H2357E1 or - Experienced a ninth new flare within the core study CACZ885H2357 and the first extension study CACZ885H2357E1 Exclusion Criteria: - Continuation in this extension study is considered inappropriate by the treating physician - Pregnant or nursing (lactating) women - Female patients being physiologically capable of becoming pregnant UNLESS they are using an acceptable method of contraception with a failure rate (Pearl Index (PI)) < 1 Other protocol defined inclusion/exclusion criteria may apply.
NCT ID:   NCT01194921
Primary Contact:   Study Director
Novartis Pharmaceuticals
Novartis Pharmaceuticals

Novartis Pharmaceuticals
Phone: +41-61-324-1111
Backup Contact:   N/A
Location Contact:   Newport News, Virginia 23606
United States



There is no listed contact information for this specific location.

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 23, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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