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临床试验/NCT01615601
NCT01615601已完成不适用

PREZISTA or INTELENCE Switch Evaluation in Virologically Suppressed Patients Naïve to Darunavir or Etravirine and Who Are Intolerant of Their Current or Prior Combination Antiretroviral Therapy Regimen: A Phase IV, Open-label, Multicentre Observational Trial

Janssen Inc.0 个研究点目标入组 77 人开始时间: 2011年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Janssen Inc.
入组人数
77
主要终点
Change from Baseline in the patient's total score of the HIV Symptom Distress Module (HIV-SDM)

研究概览

简要总结

The purpose of this study is to evaluate tolerability of darunavir (PREZISTA) or etravirine (INTELENCE) in patients infected with human immunodeficiency virus type 1 (HIV-1) who are naïve to these medications and in patients who have experienced tolerability issues on their current or prior combination antiretroviral therapy (cART). The tolerability is evaluated by switching the patients from their previous or current combination antiretroviral therapy (cART) to either darunavir or etravirine.

详细描述

This is an open label (all people know the identity of the intervention.), multicenter (study conducted at multiple sites), observational study (individuals are observed for certain outcomes) of darunavir and etravirine in patients infected with HIV-1 who are naïve to these medications and who have experienced tolerability issues on their current or prior combination antiretroviral therapy (medicines used for treatment of HIV). PREZISTA is indicated for naïve HIV patients (someone who has never used HIV drugs) and treatment-experienced HIV patients and INTELENCE is indicated for treatment-experienced patients who have failed prior therapy and have HIV-1 strains resistant to multiple antiretroviral agents (HIV-1 strains are able to survive the exposure of the multiple antiretroviral agents), including Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs). In this study patients will receive either darunavir (PREZISTA) or etravirine (INTELENCE) and physician selected optimized background agents (other antiretroviral medicines), as permitted by the local formulary and supported by the current Canadian Product Monograph. 90 patients will participate in this study (75 Patients planned for the darunavir group and 15 patients planned for the etravirine group). The total duration of the study will be 24 weeks. Safety and tolerability will be evaluated at screening (14 days prior to Day 1), baseline (patient's medical status before any treatment or research is done) at Day 1, Week 4, Week 12 and Week 24. Tolerability will be evaluated using HIV Symptom Distress Module (HIV-SDM) also referred to as the HIV Symptom Index (HSI) which is a self-completed questionnaire to evaluate symptoms and measure the presence and bothersomeness of side effects commonly seen with HIV and antiretroviral treatment over the last 4 weeks (20 questions about all symptoms which the patient might have had during the past four weeks). Higher scores indicate the presence of more symptoms and/or a greater degree of distress related to the 20 symptoms. In HIV-SDM data is collected to see the benefit of switching to either darunavir or etravirine.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have a documented HIV-1 infection
  • Have 1 or more significant symptoms with at least grade 2 toxicity on the Division of AIDS Toxicity "DAIDS grading scale" on current or prior combination antiretroviral therapy (cART) regimen (current or prior cART including regimens consisting of 2 Nucleoside reverse transcriptase inhibitors (NRTIs) and a third agent with the exception of darunavir or etravirine)
  • Have stable response to current cART ie, have an HIV-plasma viral load [number of virus in blood] at screening <400 copies/mL (undetectable) or last plasma viral load on prior regimen within the previous 6 months <400 copies/mL)
  • Must not have resistance to Primary HIV protease inhibitor medicines

排除标准

  • Has been Infected with HIV-2 - Has received previous treatment with darunavir or etravirine or non-HAART (Highly Active Antiretroviral Therapy) regimen
  • Has had prior virologic failure to 2 or more regimens or single virologic failure on prior cART
  • Has a documented resistance to darunavir and etravirine
  • Is currently using any drug contraindicated in the current Canadian Product Monograph for darunavir or etravirine

研究组 & 干预措施

etravirine (INTELENCE)

INTELENCE co-administered with other antiretroviral medicinal products as per Canadian Product Monograph (Observational Study)

干预措施: etravirine (INTELENCE) (Drug)

etravirine (INTELENCE)

INTELENCE co-administered with other antiretroviral medicinal products as per Canadian Product Monograph (Observational Study)

干预措施: Other antiretroviral medications (Drug)

darunavir (PREZISTA)

PREZISTA co-administered with 100 mg ritonavir as per Canadian Product Monograph. (Observational Study)

干预措施: darunavir (PREZISTA) (Drug)

darunavir (PREZISTA)

PREZISTA co-administered with 100 mg ritonavir as per Canadian Product Monograph. (Observational Study)

干预措施: ritonavir (Drug)

结局指标

主要结局

Change from Baseline in the patient's total score of the HIV Symptom Distress Module (HIV-SDM)

时间窗: Baseline (Day 1), Week 4, 12 and 24

HIV-SDM is a questionnaire consisting of 20 questions related to all the symptoms which the patient might have had during the past four weeks. For each question patient has to select appropriate answer related to the symptoms: "0 = I do not have this symptom; 1 = I have this symptom and it doesn't bother me; 2 = it bothers me a little; 3 = it bothers me; 4 = it bothers me a lot". Total score of HIV-SDM is then calculated for all the 20 items.

次要结局

  • Number of participants with Maintenance/achievement of virologic suppression at Week 24(Baseline and Week 24)
  • Number of participants with disappearance by Week 4 of at least one bothersome symptom identified at baseline by patient on HIV-SDM(Baseline and Week 4)
  • Number of participants with maintenance of disappearance by Week 12 and Week 24 of at least one bothersome symptom identified at baseline by patient on HIV-SDM(Baseline, Week 12 and Week 24)
  • Number of participants with Maintenance/increase in CD4 cell count.(Baseline and Week 24)
  • Comparison of change in HIV-SDM scores between those participants who were on or off ARTs at baseline(Baseline, Week 4, Week 12 and Week 24)

研究者

发起方
Janssen Inc.
申办方类型
Industry
责任方
Sponsor

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