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OpenTrials
Completed

NCT Number: NCT01613157

Predictors of Antiretroviral Pharmacokinetics in HIV-infected Women With Virologic Suppression

The investigators would like to carry out this study to measure drug levels in HIV-infected women that are taking anti-HIV medications. This study will determine the predictors of high drug levels and will assess the association of drug levels and adverse events in women.

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Key information

About this study

There have been tremendous advances in the treatment of HIV by combining 3 to 4 of the 20 anti-HIV medications available. Despite these advances, there remain several important complications related to the treatment, most importantly adverse events like nausea, diarrhea, liver toxicity and lipodystrophy (fat wasting or accumulation). Some studies have found that drug levels are higher in women and that these higher drug levels are associated with the increased toxicity in women. The reasons for the higher drug levels remain unclear. It is unknown whether these relate to hormonal influences, drug metabolism, adherence, fat distribution, body size or other factors. For this reason, we would like to carry out this study to measure drug levels in HIV-infected women that are taking anti-HIV medications. This study will determine the predictors of high drug levels and will assess the association of drug levels and adverse events in women.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Are HIV infected
  • Are 18 years old or older
  • A biologic woman
  • Are taking their first combination Anti-retroviral regimen that includes a Protease Inhibitor or a Non-Nucleoside Reverse Transcriptase Inhibitor for the past three months with no changes in any part of the combination in that period
  • Are taking either a Protease Inhibitor or an Non-Nucleoside Reverse Transcriptase Inhibitor but not both
  • If taking a Protease Inhibitor, must be taking only one Protease Inhibitor excluding low dose ritonavir used as boosting
  • Have a viral load < 50 copies/mL on two occasions at least 1 month apart including a value at least three months before the baseline visit
  • Have signed and dated a full informed consent

Exclusion criteria

  • Have difficulty participating in a trial due to non-adherence or substance abuse
  • Pregnant or breast-feeding
  • Have malignancy receiving systemic chemotherapy
  • Have end-stage organ disease
  • Have another significant non-HIV underlying disease that might impinge upon disease progression or death

Sponsors and collaborators

Lead sponsor

Canadian Immunodeficiency Research Collaborative

Other

Registry information

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Jun 7, 2012
Registry last updated
Jun 7, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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