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临床试验/NCT00002147
NCT00002147已完成3 期

Use of Stealth Liposomal Doxorubicin HCl ( DOX-SL ) in the Treatment of Moderate to Severe AIDS-Related Kaposi's Sarcoma.

Sequus Pharmaceuticals2 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
3 期
状态
已完成
发起方
试验地点
2

研究概览

简要总结

To provide Stealth liposomal doxorubicin hydrochloride ( DOX-SL ) as a therapy for Kaposi's sarcoma patients who have no remaining treatment options other than DOX-SL or patients who have been participating in another DOX-SL protocol and for whom continuation in DOX-SL is medically indicated. Also, to evaluate the safety and efficacy of DOX-SL in patients with Kaposi's sarcoma who have previously received systemic chemotherapy with or without an anthracycline.

详细描述

Patients receive DOX-SL every 3 weeks for up to 20 cycles.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have:
  • AIDS-related Kaposi's sarcoma that requires systemic chemotherapy.
  • EITHER a medical indication for continuation of DOX-SL following treatment on another DOX-SL protocol, OR no remaining treatment options other than DOX-SL.
  • Prior Medication:
  • Prior anthracyclines.

排除标准

  • Co-existing Condition:
  • Patients with the following symptoms or conditions are excluded:
  • Cardiac ejection fraction < 50 percent or clinically significant cardiac disease.
  • Eligibility for a Liposomal Technology comparative protocol.
  • Concurrent Medication:
  • Other cytotoxic chemotherapy.
  • Patients with the following prior condition are excluded:
  • History of idiosyncratic or allergic reaction to anthracyclines.
  • Prior Medication:
  • Chemotherapy within the past 3 weeks.

研究者

发起方
Sequus Pharmaceuticals
申办方类型
Industry

研究点 (2)

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