EUCTR2005-002207-16-GB进行中(未招募)1 期
A randomised controlled trial of Myfortic versus Mycophenolate Mofetil in the treatment of multi-system autoimmune disease. - MYFMAD
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •Inclusion (requires all three)
- •i)Diagnosis of SLE or PSV
- •ii)Either: about to commence MMF, or established on MMF for at least three months but with inadequate disease control on MMF 2000mg/day or less
- •iii)Written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •b)Exclusion
- •i)Active infection (including hepatitis B, C, HIV and tuberculosis)
- •ii)Known hypersensitivity to MMF
- •iii)cancer or an individual history of cancer (other than resected basal cell skin carcinoma)
- •iv)Females who are pregnant, breast feeding, or at risk of pregnancy and not using a medically acceptable form of contraception
- •v)Any condition judged by the investigator that would cause the study to be detrimental to the patient
- •vi)Use of any investigational drug within four weeks of the baseline visit
- •vii)Patients who are planning to undergo elective surgery during the study period
- •viii)Age < 18 years
研究者
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