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临床试验/NCT00166842
NCT00166842Unknown4 期

Effects of Conversion From Sirolimus Oral Solution to Tablets in Renal Transplant Recipients.

National Taiwan University Hospital2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2002年9月最近更新:
适应症
相关药物

试验速览

阶段
4 期
入组人数
40
试验地点
2
主要终点
Pharmacokinetics of sirolimus tablets in different regimens in de novo renal transplant patients

研究概览

简要总结

The purpose of this study is to understand the pharmacokinetics of sirolimus tablets in different regimens in newly renal transplant patients, and the effect of dosage form conversion on the concentration of sirolimus in stable renal transplant patients. So that we can design a better tacrolimus or cyclosporine/sirolimus/steroid dose regimen for Taiwanese.

详细描述

Sirolimus tablets will be available more than one year after the launch of sirolimus solution. Most patients on sirolimus solution will use sirolimus tablet instead.

The purpose of this study is to understand the pharmacokinetics of sirolimus tablets in different regimens in newly renal transplant patients, and the effect of dosage form conversion on the concentration of sirolimus in stable renal transplant patients. So that we can design a better tacrolimus or cyclosporine/sirolimus/steroid dose regimen for Taiwanese.

研究设计

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

入排标准

年龄范围
13 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ages of 18 and 65, renal transplant patients

排除标准

  • pregnancy, tuberculosis, hepatitis B or C carrier status, human immunodeficiency virus-positive status, retransplantation or multiorgan transplantation, or history of rheumatoid arthritis before transplantation

结局指标

主要结局

Pharmacokinetics of sirolimus tablets in different regimens in de novo renal transplant patients

Effect of dosage form conversion on sirolimus concentration in stable renal transplant patients.

次要结局

  • Effectiveness of different sirolimus dose regimens in rejection prevention

研究者

申办方类型
Other

研究点 (2)

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