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临床试验/NCT00002165
NCT00002165已完成不适用

Viracept Expanded Access Program

Agouron Pharmaceuticals1 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:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
试验地点
1

研究概览

简要总结

To make nelfinavir mesylate (Viracept) available for treatment of HIV positive patients who are unable to take the three commercially available protease inhibitors (because of failure, intolerance, or contraindication) and who have a CD4 cell count of <= 50. To obtain additional information on the safety profile of nelfinavir mesylate (Viracept).

(PER AMENDMENT 1/8/97: People now qualify for the Viracept Program if they are unable to take indinavir and/or ritonavir due to intolerance, contraindication or prior failure.)

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
All
接受健康志愿者
否

入选标准

  • •Patients must have:
  • •HIV infection.
  • •CD4 T cell count <= 100 cells/mm
  • •Failed, been intolerant of or had a contraindication to all three commercially available protease inhibitors (saquinavir, indinavir and ritonavir).
  • •(PER AMENDMENT 1/8/97:
  • •People now qualify for the Viracept Program if they are unable to take indinavir and/or ritonavir due to intolerance, contraindication or prior failure.)

排除标准

  • •Prior Medication:
  • •Prior therapy with Viracept.
  • •Indinavir.
  • •Saquinavir.
  • •Ritonavir.

研究者

发起方
Agouron Pharmaceuticals
申办方类型
Industry

研究点 (1)

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