Changes in Cerebral Function in Treatment Naive HIV-1 Infected Subjects Commencing Either Boosted Atazanavir With Truvada or Boosted Darunavir With Maraviroc and Kivexa (CogUK)
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Purpose
The purpose of this study is to compare two different combination anti-HIV therapies over 48 weeks and to assess if differences in improvement in the function of the brain are observed over this period.
The study will compare anti-HIV therapy combinations which are currently in use.
The patients will not have had any previous treatment for their HIV infection.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Impaired Cognition |
Drug: standard care Drug: novel treatment |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Randomised, Prospective Study, Assessing Changes in Cerebral Function in Treatment Naive HIV-1 Infected Subjects Commencing Either Boosted Atazanavir With Truvada or Boosted Darunavir With Maraviroc and Kivexa. |
- cognitive function [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
When commencing antiretroviral therapy (anti-HIV therapy) for the first time, improvements in the function of the brain are frequently observed. For example memory and concentration may improve. However, whether these improvements may differ between different anti-HIV therapies is largely unknown.
The purpose of this study is to compare two different combination anti-HIV therapies over 48 weeks and to assess if differences in improvement in the function of the brain are observed over this period.
- brain function [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]The study team will assess the brain functions at each visit. Also the blood will be monitored for efficacy of treatment in the two study limbs at all visits (this is part of normal care). Likewise the results of the MRI scans will be compared. The lumbar puncture performed at the final visit will obtain samples of CSF and certain test will be performed on this to examine the differences between the two study treatments. The comparison of the scan and lumbar puncture results will indicate how the brain is differently effected with different treatments.
| Estimated Enrollment: | 50 |
| Study Start Date: | January 2013 |
| Estimated Study Completion Date: | January 2015 |
| Estimated Primary Completion Date: | January 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: standard care
treatment with:
|
Drug: standard care
|
Active Comparator: Novel therapeutic approach
|
Drug: novel treatment
|
Detailed Description:
Impairment in neurocognitive(NC) function in HIV-infected subjects in the current anti-retroviraltreatment (cART) era has been associated with poor compliance with cART, reduced quality-of-life and increased mortality. Reported factors associated with the development of NC function impairment in HIV disease and risks associated with progression of such impairment include degree of immune suppression related to HIV infection, other chronic viral infections (such as chronic hepatitis C co-infection), age and central nervous system (CNS) antiretroviral drug exposure.
One modifiable factor which may be associated with the evolution of NC function impairment is the direct effect of cART on the central-nervous-system (CNS). Certain antiretroviral drugs such as zidovudine, lamivudine, abacavir, nevirapine, efavirenz and indinavir are known to achieve optimal exposure in the cerebro-spinal-fluid (CSF) whereas other drugs, such as the majority of the HIV-1 protease inhibitors penetrate less effectively. Studies to date suggest different cART regimens may have differing effects on NC performance. In the EuroSIDA study, the use of nucleoside-reverse-transcriptase inhibitors was found to specifically protect against the development of HIV related brain disease. More recently, in a small prospective study, ALTAIR, different effect on cerebral function was reported in subjects randomised to commence three different cART regimens.
The investigators propose, in a prospective, randomised study to assess the effects of two different antiretroviral regimens on NC function in HIV infected subjects commencing antiretroviral therapy for the first time.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- HIV-1 infected males or females
- signed informed consent
- no previous antiretroviral treatment since HIV diagnosis
- screening CD4+ lymphocyte count <= 350 cells/ųL
- susceptible to all currently licensed (Nucleoside Reverse Transcriptase Inhibitors) NRTIs, (Non-Nucleoside Reverse Transcriptase Inhibitors) NNRTIs and PIs based on HIV-1 genotypic resistance report
- CCR5-tropic HIV based on genotypic resistance testing*
Exclusion Criteria:
• existing neurological disease
- hepatitis B or hepatitis C co-infection
- age under 18 years
- screening laboratory parameters > grade 2 (with the exception of cholesterol and triglycerides)
- current history of major depression or psychosis
- recent head injury (past three months)
- current alcohol abuse or drug dependence
- active opportunistic infection or significant co-morbidities
- patients who are receiving other concomitant medication which are not permitted, as listed in appendix 2
female patients of child-bearing potential who:
- have a positive serum pregnancy test at screening or during the study
- are breast feeding
- are planning to become pregnant
- all participants unwilling to use a barrier method of contraception
- patients who in the opinion of the investigator are not candidates for inclusion in the study
Contacts and Locations| Contact: Andrew Whitehouse, MBBS | 02075943413 | a.whitehouse@imperial.ac.uk |
| Contact: Alan Winston, MD | a.winston@imperial.ac.uk |
| United Kingdom | |
| Birmingham Heartlands Hospital: | Recruiting |
| Birmingham, United Kingdom | |
| Principal Investigator: Steve Taylor, FRCP | |
| Brighton and Sussex University Hospital NHS Trust: | Recruiting |
| Brighton, United Kingdom, BN1 9RE | |
| Principal Investigator: Martin Fisher, FRCP | |
| Chelsea and Westminster Hospital NHS Trust | Recruiting |
| London, United Kingdom, SW10 9NH | |
| Principal Investigator: Mark Nelson, FRCP | |
| St. Thomas' Hospital | Recruiting |
| London, United Kingdom | |
| Principal Investigator: Ranjababu Kulasegaram, MD | |
| Kings College Hospital | Recruiting |
| London, United Kingdom, SE5 9RJ | |
| Principal Investigator: Frank Post, MD PhD | |
| St. Mary's Hospital | Recruiting |
| London:, United Kingdom, W2 1NY | |
| Principal Investigator: Alan Winston, MD | |
More Information
No publications provided
| Responsible Party: | Naomi Gardner, PRS Administrator, Imperial College London |
| ClinicalTrials.gov Identifier: | NCT01367236 History of Changes |
| Other Study ID Numbers: | 1733, 2011-002656-14 |
| Study First Received: | June 3, 2011 |
| Last Updated: | April 3, 2013 |
| Health Authority: | United Kingdom: Medicines and Healthcare Products Regulatory Agency |
Additional relevant MeSH terms:
|
HIV Protease Inhibitors Anti-HIV Agents Cognition Disorders Delirium, Dementia, Amnestic, Cognitive Disorders Mental Disorders Atazanavir Darunavir Protease Inhibitors |
Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Anti-Retroviral Agents Antiviral Agents Anti-Infective Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 16, 2013