FYU-981 or Benzbromarone are administrated to hyperuricemia patients with or without gout for 14 weeks to compare the efficacy and safety of these drugs by the method of multicenter, randomized, double-blind, ascending dose regimen.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
201
Oral daily dosing for 14 weeks
Oral daily dosing for 14 weeks
Tokyo
Tokyo, Japan
Percent reduction from baseline in serum urate level at the final visit
Percent reduction from baseline in serum urate level at the final visit
Time frame: 14 weeks
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