articleArthritis Care & ResearchOct 30, 2008Closed access

Effects of febuxostat versus allopurinol and placebo in reducing serum urate in subjects with hyperuricemia and gout: A 28‐week, phase III, randomized, double‐blind, parallel‐group trial

Philadelphia VA Medical Center · University of Pennsylvania · +3 more institutions

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Abstract

Abstract Objective To compare the urate‐lowering efficacy and safety of febuxostat, allopurinol, and placebo in a large group of subjects with hyperuricemia and gout, including persons with impaired renal function. Methods Subjects (n = 1,072) with hyperuricemia (serum urate level ≥8.0 mg/dl) and gout with normal or impaired (serum creatinine level >1.5 to ≤2.0 mg/dl) renal function were randomized to receive once‐daily febuxostat (80 mg, 120 mg, or 240 mg), allopurinol (300 or 100 mg, based on renal function), or placebo for 28 weeks. Results Significantly ( P ≤ 0.05) higher percentages of subjects treated with febuxostat 80 mg (48%), 120 mg (65%), and 240 mg (69%) attained the primary end point of last 3…

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Authors

8

Topics & keywords

Keywords
  • Febuxostat
  • Hyperuricemia
  • Gout
  • Allopurinol
  • Medicine
  • Placebo
  • Internal medicine
  • Renal function
UN Sustainable Development Goals
  • Good health and well-being
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