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临床试验/NCT00023426
NCT00023426已完成2 期

TBTC Study 25:A Prospective, Randomized, Double-Blind Study of the Tolerability of Higher Doses of Rifapentine

Centers for Disease Control and Prevention43 个研究点 分布在 2 个国家目标入组 150 人开始时间: 1999年7月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
150
试验地点
43
主要终点
Proportion of patients who fail to complete therapy in each of the dosing groups

研究概览

简要总结

Randomized, double-blind study of the tolerability of three different doses of rifapentine

详细描述

Prospective, randomized, double-blinded, comparative study. Patients are randomized at the completion of induction phase therapy. Sample-size is 50 HIV-seronegative patients with culture-positive, drug susceptible TB in each treatment arm. The first 75 patients will be randomized 2:1 to 900 mg:600 mg rifapentine. The second 75 patients will be randomized 2:1 to 1200 mg:600 mg rifapentine. The DSMB will review tolerability and safety data on the first 21 patients enrolled (at the 900 mg and 600 mg doses) and approve proceeding to enrollment at the 1200 mg dose.

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
Double

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Proportion of patients who fail to complete therapy in each of the dosing groups

次要结局

  • 1. Rate of serious adverse events in each of the dosing groups
  • 2. Rate of total adverse events in each of the groups
  • 3. Rate of relapse in patients with positive sputum culture at 2 months, in each of the groups

研究者

研究点 (43)

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