TRTMNT W/TENOFOVIR DF,EMTRICITABINE,& LOPINAVIR/RITONAVIR VS NO THERAPY IN HIV
TRTMNT W/TENOFOVIR DF,EMTRICITABINE,& LOPINAVIR/RITONAVIR VS NO THERAPY IN HIV
批准号:
7719483
负责人:
Elizabeth Connick
金额:
$0.41万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-04-01 至 2008-05-31
关键词:
Adverse effectsAnti-HIV AgentsBloodCD4 Lymphocyte CountChronicComputer Retrieval of Information on Scientific Projects DatabaseDrug usageEarly DiagnosisEarly treatmentFundingGrantGuidelinesHIVHIV InfectionsImmune System PartImmune systemInfectionInstitutionLearningLopinavir/RitonavirMedicinePersonsPharmaceutical PreparationsResearchResearch PersonnelResourcesRunningSourceSymptomsTenofovirTimeUnited States Food and Drug AdministrationUnited States National Institutes of HealthViral Load resultVirusdesignemtricitabinefightingimproved
中文摘要
这个子项目是许多研究子项目中利用
资源由NIH/NCRR资助的中心拨款提供。子项目和
调查员(PI)可能从NIH的另一个来源获得了主要资金,
并因此可以在其他清晰的条目中表示。列出的机构是
该中心不一定是调查人员的机构。
这项研究是为了了解在艾滋病毒感染早期治疗是否有益。换句话说,这项研究将评估抗艾滋病毒药物(替诺福韦DF、恩曲他滨和卡莱特拉)的组合对最近感染艾滋病毒的人有多安全和有效。众所周知,联合抗艾滋病毒药物可以降低血液中的病毒数量(病毒载量),改善免疫系统。然而,这些药物也有短期和长期的副作用,在人们决定是否开始抗艾滋病毒药物时也会考虑这些副作用。随着我们对抗艾滋病毒药物及其好的和坏的影响有了更多的了解,艾滋病毒治疗专家关于何时开始抗艾滋病毒药物的意见确实发生了变化。这项研究中使用的三种药物已获得美国食品和药物管理局(FDA)的批准,用于治疗慢性艾滋病毒感染者。
有针对已确定的慢性艾滋病毒感染者的治疗指南。我们不知道最近感染艾滋病毒的人的情况是否会有所不同。几年来,研究人员一直在研究最近感染艾滋病毒的人,有一些证据表明,积极治疗感染早期确诊的人可能会有一些好处。如果及早开始治疗,免疫系统中对抗艾滋病毒感染的部分可能会得到更好的保护。艾滋病毒感染的早期治疗可能会降低感染传播给另一个人的可能性。然而,我们仍然不知道从长远来看,治疗早期艾滋病毒感染是否会有所不同。我们不知道与提早开始治疗相关的副作用是否合理。
在这项研究中,一组受试者将被告知立即开始服用为期9个月的抗艾滋病毒药物。没有开始抗艾滋病毒药物的受试者,只有当他们的CD4+计数降低或病毒载量长期保持在高水平时,才会开始抗艾滋病毒药物。在研究结束时,在研究开始时接受抗艾滋病毒药物的人的病毒载量将与没有开始抗艾滋病毒药物的人的病毒载量进行比较,以查看接受9个月治疗的受试者的病毒载量是否较低。我们确实知道,保持较低病毒载量的人往往比病毒载量较高的人做得更好。
这项研究旨在使任何因病毒载量高、免疫系统下降或与艾滋病毒感染有关的症状而需要治疗的人都能得到治疗。
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
This study is being done to learn if treating people during early HIV infection is beneficial. In other words, this study will evaluate how safe and effective a combination of anti-HIV drugs (Tenofovir DF, Emtricitabine and Kaletra) is for people with recently acquired HIV infection. It is known that combination anti-HIV drugs decreases the amount of virus in the blood (viral load) and improve the immune system. However, these drugs also have short-term and long-term side effects that are also considered when people decide whether or not to begin anti-HIV medicine. The opinions of HIV treatment experts regarding when to start anti-HIV medicine do change as we learn more about the anti-HIV drugs and their good and bad effects over time. The three drugs used in this study have been approved of by the U.S. Food and Drug Administration for the treatment of people with chronic HIV infection.
There are treatment guidelines for persons with chronic, established HIV infection. We do not know if the situation may be different for persons recently infected with HIV. For several years, investigators have been studying people with recently acquired HIV infection, and there is some evidence that aggressively treating people diagnosed early during their infection may be of some benefit. The part of the immune system that fights HIV infection may be better preserved if treatment is begun early. Early treatment of HIV infection may possibly make it less likely that the infection is spread to another person. However, we still do not know whether or not treating early HIV infection makes a difference in the long run. We do not know if the side effects associated with beginning treatment earlier are justified.
During this study, one group of subjects will be told to immediately begin taking anti-HIV drugs for 9 months. The subjects who do not begin anti-HIV drugs, will start anti-HIV drugs only if their CD4+ count goes low or their viral load stays high for a long period of time. At the end of the study, the viral load in persons who received anti-HIV drugs at the beginning of the study will be compared to the viral load in persons who did not start anti-HIV drugs, to see if the subjects who received the 9 months of treatment have a lower viral load. We do know that people who keep lower viral loads tend to do better than people with higher viral loads.
This study is designed so that anyone who needs treatment for HIV because of high viral load, immune system decline or symptoms related to HIV infection will be offered treatment.
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