Treataware

Elvitegravir versus raltegravir

This trial is enrolling now. Depending on eligibility and available places in your area, you may be able to enrol in this trial.

About this trial

This study is looking at the safety, tolerability and efficacy of elvitegravir, a new protease inhibitor, boosted with ritonavir.

They are comparing the drug to the newly approved integrase inhibitor - raltegravir.

People who are treatment experienced will be given either drug with a background regimen including another protease inhibitor.

Official title:A Multicenter, Randomized, Double-Blind, Double-Dummy, Phase 3 Study of the Safety and Efficacy of Ritonavir-Boosted Elvitegravir (EVG/r) Versus Raltegravir (RAL) Each Administered With a Background Regimen in HIV-1 Infected, Antiretroviral Treatment-Experienced Adults
What is this trial studying?New drug
Start date:August 2008

This may be the proposed or expected start date for trials which have not yet started.

How many participants will this trial enrol?700

The exact number of participants may be lower or slightly higher than this. Some trials also have specific quotas for participants from each state, city or clinic.

How long is this trial planned to go for?Participants in this trial will be asked to take the trial drug for 48 weeks.
Who can enrol in this trial?You may be eligible to participate in this trial if you meet the following criteria:
  • At least 18 years old
  • Have taken HIV treatments in the past
  • Currently taking HIV treatments
  • Viral load at least 1000 copies/ml
This is a summary of key inclusion and exclusion criteria for this trial. There may be other criteria which may exclude some people from participation in this trial. Some laboratory tests may also be required. Consult your doctor, or view the trial protocol or informed consent documentation to see the full range of exclusion and inclusion criteria.
Links to further information:
Keywords:elvitegravir, raltegravir, ritonavir

If you are interested in enrolling in this trial

Before making the decision to participate in any clinical trial, NAPWA recommends that you discuss the potential benefits and risks of participation with your treating doctor. Your doctor can also provide advice about your eligibility to participate in the trial.

  • You can print this page to take it with you to the doctor – just use your browser's 'print' function.
  • Before making the decision to participate in any clinical research, read our background information.
  • Call the Treataware info line if you need further advice
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This information was retrieved from the Treataware website (www.treataware.info) on 2 Dec 2008. For further information, please consult the website or call the NAPWA office on 02 8568 0300.