NCT00002280已完成不适用
An Open Label Study Regimen of Videx (2',3'-Dideoxyinosine, ddI) in Children With Acquired Immunodeficiency Syndrome (AIDS) Who Have Demonstrated Significant Deterioration or Intolerance to Zidovudine (Retrovir)
Bristol-Myers Squibb2 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
- 2
研究概览
简要总结
The purpose of this study is to make didanosine (ddI) available to children with AIDS who are clinically deteriorating on zidovudine (AZT) or intolerant to AZT and cannot enter the Phase II ddI programs due to protocol exclusion or geographic location.
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
- 3 Months 至 12 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究者
研究点 (2)
Loading locations...
相似试验
已完成
不适用
A Study of ddI in Patients With AIDS Who Become Sicker While Taking ZidovudineLeukoencephalopathy, Progressive MultifocalHIV InfectionsNCT00002274Bristol-Myers Squibb
已完成
不适用
A Treatment IND (Investigational New Drug) Protocol for the Use of Videx (2',3'-Dideoxyinosine, ddI) in Patients With Acquired Immunodeficiency Syndrome (AIDS) or AIDS- Related Complex (ARC) Who Are Intolerant to Zidovudine (Retrovir)HIV InfectionsNCT00002028Bristol-Myers Squibb
暂停
2 期
Bioequivalence Study of Didanosine in Children Treated for HIVHIV InfectionsNCT00668356Assistance Publique - Hôpitaux de Paris26
已完成
2 期
One Month Dual Antiretroviral Prophylaxis to Prevent Resistance Mutations in Mothers Exposed to Single Dose NevirapineHIV InfectionsNCT00142337Institut de Recherche pour le Developpement244
已完成
2 期
Safety and Effectiveness of a Three-Drug Combination Treatment for Recently Infected or Converted HIV PatientsHIV InfectionsNCT00007202National Institute of Allergy and Infectious Diseases (NIAID)55