Safety and Efficacy of Oral Febuxostat in Subjects With Gout

NCT02082769 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 504

Last updated 2016-02-03

Study results available
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Summary

The purpose of this study is to compare febuxostat allopurinol in subjects with gout.

Conditions

Interventions

DRUG

Febuxostat

DRUG

Allopurinol

Sponsors & Collaborators

  • Qingdao Shengbang Pharmaceutical Co., Ltd.

    collaborator INDUSTRY
  • Xijing Hospital

    lead OTHER

Principal Investigators

  • Shenren Chen, M.D. · Second Affiliated Hospital of Shantou University Medical College

  • Yangang Wang, M.D. · The Affiliated Hospital of Qingdao University

  • Xiumei Liu, M.D. · The First Affiliated Hospital of Shanxi Medical University

  • Hong Liu, M.D. · First Affiliated Hospital of Guangxi Medical University

  • Yongde Peng, M.D. · Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

  • Jianqin Wang, M.D. · Lanzhou University Second Hospital

  • Jinying Lin, M.D. · People's Hospital of Guangxi Zhuang Autonomous Region

  • Haiwang Ji, M.D. · Shaanxi Provincial People's Hospital

  • Bin Liu, M.D. · The First Hospital of Jilin University

  • Ying Lu, M.D. · Zhejiang Provincial Tongde Hospital

  • Peng Liu, M.D. · Guangxi Ruikang Hospital

  • Yonghong Zhang, M.D. · Luoyang Orthopedic-Traumatological Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2013-10-31
Completion
2013-10-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02082769 on ClinicalTrials.gov