EUCTR2005-000028-17-ES招募中不适用
Eficacia virológica, inmunológica y trascendencia clínica del efecto de la lamivudina en pacientes portadores de la mutación M184V/I con fracaso terapéutico.
DAVID DALMA0 个研究点开始时间: 2006年4月4日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Age > or =18 years old.
- •Confirmed diagnosis of HIV-1 infection.
- •Sign informed consent.
- •Previous antiretroviral treatment must not be modified in the previous 3 months.
- •Viral load > 1000 copies/ml at the inclusion time.
- •Analysis of genotypic resistance with presence of M184V/I mutation.
- •Presence in genotypic test of M184V + 2 mutations to the following:
- •Nucleoside analog (M41L, D67N, K64R, K70R, L74V, V75I/T/M/S/A, L210W, T215Y/F, K219Q/E/N, Q151M, T69S, E44D, V118I).
- •Protease inhibitor (D30N, L33I/F/V, M46I/L, G48V, I50V/L, I54V, V82A/F/I/T/S, I84V, L90M).
- •No nucleoside analog (K103N, L100I, V106A, V108I, Y181C/I, Y188L, G190S/A).
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Active infection in the previous month.
- •Pregnancy woman or women willing to be pregnant during the study.
- •Selection of lamivudine in the rescue treatment of the patient.
- •Inclusion of emtricitabine in the rescue treatment of the patient.
研究者
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