跳至主要内容
临床试验/NCT00005921
NCT00005921已完成不适用

An Open, Serial-Panel, Multiple-Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of L-743,872 in Patients With Candida Esophagitis

Merck Sharp & Dohme LLC1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2001年8月31日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
1

研究概览

简要总结

The purpose of this study is to see if it is safe to give L-743,872 to men with candidal esophagitis, an AIDS-related yeast infection in the esophagus.

详细描述

In this open-label study, patients receive intravenous L-743,872 every 24 hours at one of three dose levels for 14 days. Post-study safety evaluations continue for 4 weeks after the final dose. Pharmacokinetics and safety measurements are taken throughout the 6-week study.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •You may be eligible for this study if you:
  • •Are an 18- to 65-year-old man with candidal esophagitis.

排除标准

  • 未提供

研究者

申办方类型
Industry

研究点 (1)

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