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临床试验/NCT05936281
NCT05936281已完成2 期

A Randomized, Open-lable, Multi-center, Active-controlled Phase 2 Study for Evaluating Efficacy and Safety of Genakumab in Prevention of Acute Flares in Gout Patients Initiating Urate-lowering TherapyUrate-lowering

Changchun GeneScience Pharmaceutical Co., Ltd.1 个研究点 分布在 1 个国家目标入组 165 人开始时间: 2023年7月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
165
试验地点
1
主要终点
Mean Number of Gout Flares Per Participant

研究概览

简要总结

To evaluate the safety and efficacy of Genakumab in prevention of acute flares in gout patients initiating urate-lowering therapyurate-lowering

详细描述

A randomized, open-lable, multi-center, active-controlled Phase 2 study. Patients are randomized to Genakumab 100mg single injection group, Genakumab 200mg single injection group or oral colchicine 0.5mg once a day.for 12 weeks group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Genakumab group

Experimental

Genakumab 100mg single injection、Genakumab 200mg single injection

干预措施: Genakumab for injection (Drug)

Colchicine group

Active Comparator

Oral colchicine 0.5mg once a day for 12 weeks

干预措施: Colchicine (Drug)

结局指标

主要结局

Mean Number of Gout Flares Per Participant

时间窗: Baseline to Week 12

次要结局

  • Proportion of Participants With at Least 1 Gout Flare Within 12 Weeks After Randomization(Baseline to Week 12)
  • Time from Randomization to the First Flare(Baseline to Week 12)
  • Mean duration of flares(Baseline to Week 12)
  • 5. Percentage of Participants With Treatment Emergent Adverse Events (TEAEs)(Baseline to Week 12)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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