Study Description
Screening
Study Centers
Contact/Consent
Gout Study - H2357
The purpose of this randomized, controlled study is to evaluate the efficacy of a Novartis investigative drug in relieving pain from the acute gout flare and preventing recurrence of new gout flares, in sufferers that are either intolerant or non-responsive to traditional non-steroidal anti-inflammatory drugs (NSAIDs) and/or colchicine treatments.
An investigational drug is a drug that is being tested and is not approved for sale in the United States by the Food and Drug Administration (FDA).
Trial phase:
Phase 3
Participation Duration:
Participants will be required to visit the study center 7 times over a 3 month period. Three additional visits will be required for each acute gout flare up..
Protocol Number:
CACZ885H2357
The next step is to see if you (or the participant) meet the
basic criteria required for participation in this clinical trial.
Please fill out the questionnaire below to see if you (or the
participant) may be suitable for the clinical trial. Your answers to
these questions are not retained by this system. You must answer the
questions below for yourself, or, you must be the legally authorized
representative of the potential participant in order to answer the
questions on their behalf. If you (or the participant) do not meet
the preliminary qualifications, you may search for other clinical
trials of interest or sign up to the Mailing List.
Answers to all questions are required to determine if you meet
the preliminary qualifications for the study.
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