Phase III Trial of Tetrathiomolybdate (TM) in Primary Biliary Cirrhosis
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 29
- 试验地点
- 1
- 主要终点
- Improvement in drug treated group vs placebo group in two liver function tests and one serum cytokine measurement
研究概览
简要总结
The University of Michigan is conducting a study investigating a potential new treatment aimed at slowing/halting progression of primary biliary cirrhosis. This will be a 2 arm double blind study in which half of the patients will be randomly selected to receive a placebo (capsule with no active ingredient) and half will receive the new treatment drug, tetrathiomolybdate. Neither the patient nor the treating physician will know which arm the patient is in. The length of the study for each patient is 24 months of drug therapy. Lab draws will be necessary weekly for the first 6 weeks of the study, followed by every other week for 3 weeks, and then monthly for the remainder of the 2 year period. In addition, intermittent history and physicals and urine samples will also be necessary. There is no cost to you for any experimental treatment. All patients in both arms will continue on ursodiol and receive standard of care treatment
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Generally medically healthy
- •Age 18 and older
- •Documented primary biliary cirrhosis
- •Alkaline phosphatase > 137
排除标准
- •Severe liver decompensation
- •Requirement for renal dialysis
- •Pregnancy or nursing
- •Meld score > 15 (13-15 will require a physician's clinical judgment)
- •Uncontrolled congestive heart failure
- •Severe diabetic neuropathy
- •Severe pulmonary disease
- •Advanced cancer
- •Requirement for steroid therapy
- •Uncontrolled ascites, variceal hemorrhage or spontaneous bacterial peritonitis
- •Pregnant or nursing
研究组 & 干预措施
1
Tetrathiomolybdate with ursodiol
干预措施: Tetrathiomolybdate (Drug)
2
Placebo with ursodiol
干预措施: Placebo (Other)
结局指标
主要结局
Improvement in drug treated group vs placebo group in two liver function tests and one serum cytokine measurement
时间窗: 2 years
次要结局
- Improvement in drug treated group vs placebo group in serum CRP or interleukin-1-beta-levels(2 years)
