A Pilot Study Of A Novel Treatment Regimen, Maraviroc + Ritonavir Boosted Atazanavir, In Treatment Naive HIV-Infected Patients - NCT00827112-20009 (Clinical Trial 265062)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy265062.aspx
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Washington |
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State:
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DC |
| Zip Code: |
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20009 |
| Conditions: |
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Human Immunodeficiency Virus-1 |
| Purpose: |
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This is a pilot study to examine if the novel treatment regimen maraviroc plus boosted
atazanavir can be expected to be safe and efficacious in treatment naive HIV infected
patients. Based on the results from this study, a confirmatory phase 3 study may be
conducted.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- HIV-1 RNA viral load of ≥1,000 copies/mL measured at the Screening Visit.
- CD4 count ≥100 cells/mm3 at Screening.
- Have only R5 HIV-1 at Screening as verified by the Monogram Bioscience Trofile® assay
with enhanced sensitivity.
Exclusion Criteria:
- Prior treatment with any other HIV antiretroviral therapy for more than 14 days at
any time.
- Any evidence of resistance to atazanavir, tenofovir, and emtricitabine.
- X4-or dual/mixed-tropic virus by enhanced Trofile assay or repeated assay failure or
not reportable results. |
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| Study is available at: |
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Pfizer Investigational Site
Washington, DC 20009
United States
Primary Contact:
Pfizer CT.gov Call Center
Phone: 1-800-718-1021 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 16, 2010 |
Modifications to
this listing: |
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above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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