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临床试验/NCT02534896
NCT02534896终止3 期

To Evaluate The Efficacy And Safety Of Sunpharma1505 Compared With Reference1505 In Subjects With Active Rheumatoid Arthritis

Sun Pharmaceutical Industries Limited20 个研究点 分布在 2 个国家目标入组 150 人开始时间: 2015年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
150
试验地点
20
主要终点
Good/Moderate European League Against Rheumatism Responders

研究概览

简要总结

This study is designated to evaluate the safety and efficacy of Sunpharma1505 in subjects with active rheumatoid arthritis who are experiencing a flare/exacerbation.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects able and willing to give written informed consent and is available for entire study.
  • Male or female ≥ 18 years old
  • Willing and able to comply with the study protocol visits, assessments and accessible for follow up
  • Known Diagnosed Rheumatoid arthritis
  • Subjects of child bearing potential should be non-lactating and must be practicing an acceptable method of birth control as judged by the Investigator

排除标准

  • Subjects who are pregnant or intend to become pregnant during the study
  • Subject with positive hepatitis panel and / or anti-hepatitis B core antibodies, and / or hepatitis C virus antibody [anti-HCV]), and / or a positive Human immunodeficiency virus (HIV) antibody.
  • Known sensitivity to any component of the study drug or previous hypersensitivity reaction or other clinically significant reaction to IV medications, biologic therapy or IV radiocontrast agents.
  • Active infection requiring systemic treatment
  • Planned surgery during the study period or had undergone major surgery within the 60 Days prior to the Screening visit.

研究组 & 干预措施

Treatment 1: Sunpharma1505 (Low dose) and Placebo

Experimental

干预措施: Treatment I (Drug)

Treatment II: Sunpharma1505 (High Dose) and Placebo

Experimental

干预措施: Treatment II (Drug)

Treatment III: Reference1505 and Placebo

Active Comparator

干预措施: Treatment III (Drug)

结局指标

主要结局

Good/Moderate European League Against Rheumatism Responders

时间窗: week 1

次要结局

  • Good European League Against Rheumatism -Responders(Day 8)
  • Good/Moderate European League Against Rheumatism Responders(Day 15)
  • Good European League Against Rheumatism Responders(Day 15)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (20)

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