Raltegravir With Optimized Background Therapy (OBT) in Multiple Experienced HIV-infected Patients: a Retrospective Analysis of a Portuguese Cohort Treated Within the Expanded Access Program
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 151
- 主要终点
- HIV-RNA Levels
研究概览
简要总结
The purpose of this study is to evaluate the efficacy of raltegravir with optimized background therapy (OBT) in multiple-experienced HIV infected patients, measured by the proportion of patients with undetectable viral load and the mean increase of CD4 cells count at week 24 and 48.
It is also intended to evaluate:
- viral load suppression and the mean increase of CD4 cells count at week 24 and 48 in patients who needed to change antiretroviral (ARV) therapy due to inacceptable toxicity, as determined by the investigator, including patients who needed to replace T20.
- efficacy of raltegravir with OBT in HIV-2 infected patients that were included in this cohort, measured by the percentage of patients with undetectable viral load and the mean change of CD4 cells count at week 24 and 48.
Study hypotheses:
- Raltegravir with OBT is effective in achieving and maintaining a long term virologic suppression along with a significant increase on CD4 cells count in both HIV-1 and HIV-2 infected patients.
- Patients who replaced T20 by raltegravir, due to intolerance, are able to maintain long term virologic suppression.
详细描述
Considering its novel mechanism of action, potency, safety and tolerability, and pharmacokinetic profile, raltegravir has been used in several clinical scenarios. Since its initial clinical use in multiresistant patients throughout the Expanded Access and Compassionate Use Program (started in March 2007) raltegravir has been used successfully in other clinical scenarios, including but not limited to: enfuvirtide-related serious adverse events and intolerance, nucleoside analogue inhibitors' toxicity, ritonavir and protease inhibitor intolerance and to avoid significant drug-drug interactions. Early access to raltegravir was basically focused on patients on therapeutic failure and triple-class resistance and due to enfuvirtide intolerance. In order to achieve a better understanding of the efficacy and safety profile of raltegravir in the clinical setting, it is intended to evaluate retrospectively HIV patients treated in Portugal with raltegravir since the Early Access and Compassionate Use Program (EAP) was implemented.
This is a national, multicenter, observational, clinical cohort study with retrospective collection of data. Each site will include patients who had started treatment with raltegravir under the EAP.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female patients, aged 18 years or older
- •ARV multi-experienced patients (i.e. experienced at least two prior regimens) with need to change current ARV therapy, including:
- •HIV-1 infected patients with documented therapeutic failure,
- •HIV-2 infected patients with documented therapeutic failure
- •HIV infected patients in virologic suppression who needed to change ARV due to inacceptable toxicity, as determined by the investigator, including patients who needed to replace T20
- •Raltegravir-naïve patients who initiated raltegravir since the EAP Program, with optimized background therapy(OBT)
- •Patient who has been followed at the same clinical site since the start of raltegravir
排除标准
- •Acute or decompensated chronic hepatitis. Patients with serum aminotransferase levels 10 times the upper limit of the normal range or higher (grade 4)
- •Patients who presented resistance to drugs included in OBT (namely, etravirine, darunavir or maraviroc)
- •Non-existing medical records for viral load and TCD4 at baseline, week 24 and 48
结局指标
主要结局
HIV-RNA Levels
时间窗: week 48
Patients achieving undetectable viral load (confirmed HIV RNA \< 50 copies/mL) at week 48.
CD4 Cells Count
时间窗: week 48
CD4 cells count at week 48.
次要结局
- HIV-RNA Levels(Week 48)
- Adverse Drug Reactions(Week 48)
- CD4 Cells Count(Week 48)