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临床试验/NCT00000836
NCT00000836已完成2 期

A Phase II/III Trial of Human Anti-CMV Monoclonal Antibody MSL 109 (MACRT)

National Institute of Allergy and Infectious Diseases (NIAID)6 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2001年8月31日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
300
试验地点
6

研究概览

简要总结

To compare the safety and efficacy of sevirumab (MSL 109; Protovir), human anti-cytomegalovirus (CMV) monoclonal antibody, plus active primary treatment versus placebo plus active primary treatment in AIDS patients with newly diagnosed and relapsed CMV retinitis.

Ganciclovir and foscarnet are used for treatment of CMV retinitis, but cause hematologic toxicity and nephrotoxicity, respectively. Despite continued maintenance therapy with these drugs, relapse occurs in 85 percent of patients within 4 months. Studies suggest that MSL 109, a human monoclonal antibody, when given with either ganciclovir or foscarnet, may increase initial response and prolong time to progression in patients with CMV retinitis.

详细描述

Ganciclovir and foscarnet are used for treatment of CMV retinitis, but cause hematologic toxicity and nephrotoxicity, respectively. Despite continued maintenance therapy with these drugs, relapse occurs in 85 percent of patients within 4 months. Studies suggest that MSL 109, a human monoclonal antibody, when given with either ganciclovir or foscarnet, may increase initial response and prolong time to progression in patients with CMV retinitis.

Patients are randomized to receive either MSL 109 or placebo every 2 weeks as supplemental therapy to primary CMV treatment.

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

  • •Concurrent Medication: Required:
  • •Primary CMV treatment.
  • •Patients must have:
  • •Active CMV retinitis.
  • •At least one photographable lesion of one-quarter or more optic disc area in size.
  • •Undergoing primary treatment for CMV retinitis that is not contraindicated with MSL
  • •Visual acuity in at least one eye of 3 or more letters on Early Treatment Diabetic Retinopathy Study ( ETDRS ) chart at 1 meter distance ( Snellen equivalent 5/200 ). Note:
  • •Exceptions may be made if visual acuity impairment is possibly reversible and there is at least light perception in that eye.

排除标准

  • •Co-existing Condition:
  • •Patients with the following symptoms or conditions are excluded:
  • •Retinal detachment not scheduled for surgical repair.
  • •Media opacity that precludes visualization of the fundus.
  • •Active medical problems sufficient to hinder study compliance.
  • •Concurrent Medication:
  • •CMV immune globulin ( CMVIG ).
  • •Interferon alpha.
  • •Interferon gamma.
  • •Interleukin-2 ( IL-2 ).
  • •Drug or alcohol abuse sufficient to hinder study compliance.

研究者

研究点 (6)

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