APV30002

A study testing the antiviral effectiveness of a new formulation of amprenavir.

 

Background

The standard dose of the protease inhibitor amprenavir requires individuals to take large numbers of pills. A new formulation of amprenavir may prove to be as or more effective, requiring less pills per day.
Objective
To study the safety and effectiveness of the experimental formulation of amprenavir to see if it is easier to tolerate and to take.

 

Study Design

Volunteers will be randomly assigned to one of two study groups:

Group 1: Volunteers will receive 1335 mg of the new amprenavir formulation, 200 mg of ritonavir, 300 mg of abacavir and 150 mg of 3TC.

Group 2: Volunteers will receive 1250 mg of nelfinavir, 300 mg of abacavir and 150 mg of 3TC.

Inclusion
Criteria
• Two kinds of volunteers are needed:
  1. Volunteers who have taken anti-HIV medications for less than 4 weeks.
  2. Volunteers who have never taken anti-HIV medications before.

• HIV+ male or female at least 18 years old.

• Viral load greater or equal to than 1000 copies/mL.

• If female, not pregnant and willing to use a barrier method of contraception for the duration of the study.


Status
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Enrolling
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For more information about participating in this study in the Los Angeles area, please call 310/358.2429 or e-mail Corie Castro at ccastro@aidsresearch.org

We encourage participation by women and people of color.

This ad was reviewed and approved by the AIDS Research Alliance Institutional Review Board in April, 2001.

 


 

 

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