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临床试验/NCT03394196
NCT03394196终止不适用

Implementation and Evaluation of an HIV-2 Viral Load and ARV Resistance Informed Algorithm for 2nd-line ART in HIV-2 Infected Patients in the Initiative Sénégalaise d'Accès Aux Antirétroviraux (ISAARV) Program

University of Washington2 个研究点 分布在 1 个国家目标入组 152 人开始时间: 2018年7月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
152
试验地点
2
主要终点
Loss to follow up

研究概览

简要总结

Prospective, longitudinal, open label, HIV-2 viral load and antiretroviral resistance informed 2nd-line ARV implementation study.

详细描述

Prospective, longitudinal, open label, HIV-2 viral load and antiretroviral resistance informed 2nd-line ARV implementation study.

DURATION

Up to 3 years

SAMPLE SIZE

150

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • HIV-2 infection: confirmed by Determine (Alere, Inc.) & Immunocomb II (Alere, Inc.) or equivalent
  • Failing 1st line antiretroviral therapy (e.g. AZT/3TC or TDF/XTC + LPV/r; previous 3 NRTI or 2 NRTI regimens; previous Indinavir (IDV) use, current or previous Atazanavir (ATV) use; previous NNRTI use)
  • For females of reproductive potential: negative serum or urine pregnancy test
  • Men and women age >/=18 years
  • Ability and willingness of subject to provide informed consent

排除标准

  • HIV-1 or HIV-1/HIV-2 dual infection
  • Pregnancy or Breast-feeding
  • Lab Abnormalities
  • AST/ALT >2.5 X ULN
  • CrCl <30
  • Current or previous use of Integrase Inhibitors or Darunavir

研究组 & 干预措施

No HIV-2 resistance

Experimental

干预措施: HIV-2 Genotypic Drug Resistance Testing using DBS (Diagnostic Test)

No HIV-2 resistance

Experimental

干预措施: 2nd line ART ( Zidovudine 300mg BID + Lamivudine 150mg BID or Tenofovir DF 300mg QD + Lamividine 300mg QD or Emtricitabine 200mg QD + Lopinavir/Ritonavir 400/100mg BID) (Drug)

HIV-2 NRTI resistance only

Experimental

干预措施: HIV-2 Genotypic Drug Resistance Testing using DBS (Diagnostic Test)

HIV-2 NRTI resistance only

Experimental

干预措施: 2nd line ART (Tenofovir DF 300mg QD + Lamividine 300mg QD or Emtricitabine 200mg QD + Lopinavir/Ritonavir 400/100mg BID + Raltegravir 400mg BID ) (Drug)

HIV-2 NRTI and PI resistance

Experimental

干预措施: HIV-2 Genotypic Drug Resistance Testing using DBS (Diagnostic Test)

HIV-2 NRTI and PI resistance

Experimental

干预措施: 2nd line ART (Tenofovir DF 300mg QD + Lamividine 300mg QD or Tenofovir DF 300mg QD + Emtricitabine 200mg QD + Darunavir 600mg BID-Ritonavir 100mg BID +Raltegravir 400mg BID) (Drug)

结局指标

主要结局

Loss to follow up

时间窗: 1 year

no contact with study for 1 year

Virologic Failure on 2nd line ART

时间窗: up to 3 years

VL \>250 copies/ml

HIV-2 ARV resistance on 2nd line ART

时间窗: up to 3 years

by DBS genotyping

Death

时间窗: up to 3 years

all cause mortality

次要结局

  • New WHO stage 3 or 4 event > 6 months after starting ART(up to 3 years)
  • Grade 3 or 4 adverse events(up to 3 years)
  • CD4 T-cell count trajectory(up to 3 year after starting 2nd-line ART)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Geoffrey S. Gottlieb

Professor

University of Washington

研究点 (2)

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