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临床试验/RPCEC00000085
RPCEC00000085已完成4 期

Effectiveness and Safety of use ior LeukoCIM as prophylaxis and treatment of Neutropenia in patients with HIV/AIDS.

Center of Molecular Inmunology(CIM)0 个研究点开始时间: 2009年8月20日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study. Masking: Open. Control Group: Uncontrolled. Assignment: Single Group. Purpose: Treatment

入排标准

年龄范围
18 years 至 none(—)
性别
All

入选标准

  • 1.HIV/AIDS patients who are or not associated to an opportunistic malignant disease and who meet the diagnostic criteria. 2.Patients who signed their consent in order to participate in the study. 3.Patients older than 18 years. 4.Patients of both sexes.

排除标准

  • 1.Patients with known hypersensitivity to E.Coli cell products or other preparations of rG-CSF. 2.Pregnant patients or breastfeeding.

研究者

发起方
Center of Molecular Inmunology(CIM)

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