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临床试验/JPRN-jRCT2080221136
JPRN-jRCT2080221136未知3 期

Efficacy and safety of FYX-051 in hyperuricemic patients with moderate renal insufficiency

SANWA KAGAKU KENKYUSHO Co., Ltd.0 个研究点开始时间: 2010年6月25日最近更新:
适应症

试验速览

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 74age old(—)
性别
All

入选标准

  • Patients with hyperuricemia with the following serum urate level:
  • - Serum urate level of >= 7.0mg/dL in patients with history of gout, or
  • - Serum urate level of >= 8.0mg/dL in other patient
  • Patients with moderate renal insufficiency
  • - eGFR level of >= 30mL/min/1.73m2, but < 60mL/min/1.73m2

排除标准

  • Patients with gouty arthritis within two weeks before start of study treatment
  • Patients with secondary hyperuricemia
  • Patients with, or a history of, clinically significant cardiac, hematologic and hepatic disease

研究者

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