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临床试验/NCT00002355
NCT00002355已完成不适用

A Randomized Comparison of Immediate Versus Delayed Treatment With Intravitreal Injections of ISIS 2922 in Patients With Peripheral Cytomegalovirus (CMV) Retinitis

Ionis Pharmaceuticals, Inc.13 个研究点 分布在 1 个国家目标入组 60 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
不适用
状态
已完成
入组人数
60
试验地点
13

研究概览

简要总结

To determine a clinically safe and effective dose of intravitreally injected ISIS 2922 and to compare the safety and efficacy of immediate versus delayed treatment in AIDS patients with previously untreated, peripheral cytomegalovirus ( CMV ) retinitis.

详细描述

In Stage 1 (dose escalation), patients receive either 75 or 150 mcg intravitreal ISIS 2922. In Stage 2 (randomization), patients are enrolled in either the immediate treatment group or delayed treatment group. Immediate treatment consists of intravitreal ISIS 2922 every 7 days for 3 injections (Induction) then every 14 days for 18 weeks (Maintenance). Patients in the delayed treatment group receive no immediate anti-CMV treatment but are monitored weekly for disease progression. If disease progresses, patient receives ISIS 2922 on an identical dosage regimen as those on immediate treatment. Patients may continue ISIS 2922 on a biweekly extended maintenance schedule if dose is considered safe and the CMV retinitis is clinically controlled. Per 2/8/96 amendment, patients are now in Stage 2 at 150 mcg.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients must have:
  • •Clinical diagnosis of previously untreated peripheral CMV retinitis in one eye.
  • •Leading edge of a CMV retinitis lesion is at least 750 microns from zone one. NOTE:
  • •Patients with CMV retinitis in zone three only may be eligible if the lesions can be reliably photographed to follow progression.

排除标准

  • •Co-existing Condition:
  • •Patients with the following symptoms or conditions in the eye to be treated are excluded:
  • •External ocular infections.
  • •Other herpetic infections of the retina, toxoplasma retinochoroiditis, or other disease of the fundus.
  • •Ocular conditions that will obstruct visualization of the posterior ocular structures.
  • •Retinal detachment.
  • •Silicone oil in eye.
  • •Patients with the following other symptoms or conditions are excluded:
  • •Known or suspected allergy to phosphorothioate oligonucleotides.
  • •Syphilis.
  • •Pseudoretinitis pigmentosa.
  • •Concurrent Medication:
  • •Current treatment for extra-ocular CMV infection.
  • •Ganciclovir.
  • •Foscarnet.
  • •Mellaril.
  • •Stelazine.
  • •Thorazine.
  • •Clofazimine.
  • •Ethambutol/fluconazole combination.
  • •Investigational medications for CMV retinitis.
  • •Concurrent Treatment:
  • •Investigational procedures for CMV retinitis.
  • •Patients with the following prior conditions are excluded:
  • •History of surgery to correct retinal detachment in the eye to be treated.
  • •History of syphilis.
  • •Prior Medication:
  • •Prior anti-CMV retinitis treatment in either eye.
  • •Anti-CMV therapy for extra-ocular infection within the past 2 days.

研究者

申办方类型
Industry

研究点 (13)

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