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Completed

NCT Number: NCT00126880

AVX754 (a New Nucleoside Reverse Transcriptase Inhibitor [NRTI]) to Treat Drug-resistant HIV

The study will measure how safe and effective AVX754 (a new drug for the treatment of HIV) is in treating HIV-1 infected people who have failed treatment with lamivudine.

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Key information

About this study

Lamivudine or emtricitabine are commonly used in combination with other drugs for first-line treatment of HIV infection. Although effective initially, many people later on develop resistance to some or all of the drugs (including lamivudine) leading to virological failure. Resistance is associated with characteristic mutations, which for lamivudine is the M184V mutation. A change to new, active drugs must take place when patients fail their current regime, to regain control of the virus. Although there are other types of drugs available for second line treatment, there is currently no fully active, well tolerated cytidine analogue that can replace lamivudine in a second-line regimen when patients fail first line treatment. This study will measure the efficacy and safety of AVX754 (a novel cytidine analogue with activity against HIV resistant to other nucleosides) as part of a new regimen to treat patients who have failed treatment containing lamivudine, compared to the best alternative new regimen which continues to include lamivudine.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • HIV-1 infected
  • M184V mutation in reverse transcriptase
  • Currently taking lamivudine
  • Viral load >2000 copies/ml

Exclusion criteria

  • Hepatitis B surface antigen positive
  • Pregnant or breastfeeding females
  • Hepatitis C RNA positive and requiring treatment

Treatment and study plan

AVX754

Drug

apricitabine, 600mg BID or 800mg BID

Other names: apricitabine

3TC

Drug

3TC, 150mg BID

Other names: lamivudine

Primary outcomes

  1. Change from baseline in HIV RNA levels at day 21

    Time frame: day 21

  2. Time-weighted average change from baseline in HIV RNA levels through 21 days

    Time frame: 21 days

Secondary outcomes

  1. Change from baseline in HIV RNA levels at days 7, 14, 21

    Time frame: days 7, 14, 21

  2. Proportion of subjects with HIV RNA levels <400 or <50 at days 7, 14, 21, and weeks 24 and 48

    Time frame: days 7, 14, 21, and weeks 24 and 48

  3. Change from baseline and change in ratio of CD4+ and CD8+ cells at day 21 and weeks 24 and 48

    Time frame: day 21 and weeks 24 and 48

Sponsors and collaborators

Lead sponsor

Avexa

Industry

Registry information

Official study title

A Phase II, Randomised, Double-blind, Dose-ranging Study of AVX754 Versus Lamivudine in Treatment-experienced HIV-1 Infected Patients With the M184V Mutation in Reverse Transcriptase

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Aug 5, 2005
Registry last updated
Jun 23, 2011

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.

Published trials that share one or more normalized conditions with this study.