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临床试验/EUCTR2004-000948-25-ES
EUCTR2004-000948-25-ES进行中(未招募)1 期

Determinación de niveles plasmáticos e intracelulares de los inhibidores de la transcriptasa inversa análogos a nucleósidos (NRTI) y del análogo a nucleótido tenofovir disoproxil fumarato (TDF) en pacientes tratados con abacavir y/o lamivudina administrados con o sin TDF

Fundació de Lluita Contra la Sida0 个研究点目标入组 27 人开始时间: 2004年9月27日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
27

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • HIV-infected patients >18 years old
  • Indetectable viral load
  • HAART receiving treatment during previous three months including lamivudine and/or ABC and TDF, with ritonavir/lopinavir or nevirapine
  • 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

  • Interruption of the theraphy during the study
  • Concomitant treatment with other medicinal products that should interaction with antirretroviral treatment
  • Concomitant treatment with other antirretroviral drugs during the study

研究者

发起方
Fundació de Lluita Contra la Sida

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