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临床试验/JPRN-jRCT2080221035
JPRN-jRCT2080221035未知3 期

ong-Term Safety and Efficacy of FYX-051 in Patients with Hyperuricemia (with or without Gout)

SANWA KAGAKU KENKYUSHO Co., Ltd.0 个研究点开始时间: 2010年3月3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 patients with renal stones, hypertension, hyperlipidemia or diabetes, or
  • - Serum urate level of >= 9.0mg/d

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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