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临床试验/NCT00002171
NCT00002171已完成2 期

A Phase II, Randomized, Placebo-Controlled Study of the Safety and Efficacy of Viracept in Combination With Antiretroviral Therapy in HIV Positive Women With <= 1 Month of Prior Treatment With d4T and/or 3TC

Agouron Pharmaceuticals8 个研究点 分布在 1 个国家开始时间: 2001年8月31日最近更新:
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试验速览

阶段
2 期
状态
已完成
发起方
试验地点
8

研究概览

简要总结

The purpose of this study is to see if it is safe and effective to give Viracept plus stavudine (d4T) plus lamivudine (3TC) to HIV-positive women with a CD4 count <= 400 cells/mm3. This study also examines how the body handles Viracept when given with d4T and 3TC.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

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

入选标准

  • Patients must have:
  • HIV infection.
  • CD4 T cell count <= 400 cells/mm3.

排除标准

  • Prior Medication:
  • Prior therapy or less than 1 month of therapy with d4T and/or 3TC.
  • Prior protease inhibitor therapy.

研究者

发起方
Agouron Pharmaceuticals
申办方类型
Industry

研究点 (8)

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