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The purpose of the study is to assess the effect of PF-06743649 in lowering serum uric acid in subjects suffering from gout following 14 days of dosing, as well as assessing safety and tolerability.
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Lead Sponsor
Pfizer
NCT07089888 · Tophaceous Gout
NCT07453004 · Acute Gouty Arthritis
NCT07504146 · CPPD - Calcium Pyrophosphate Deposition Disease, Gout
NCT07089875 · Gout
NCT07116746 · Gout, Gouty Arthritis, and more
MRA Clinical Research, LLC
Miami, Florida
Miami Research Associates, Inc.
South Miami, Florida
Vince and Associates Clinical Research Inc.
Overland Park, Kansas
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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.
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