CNA 30032

A study looking at why some patients develop a hypersensitivity reaction (serious allergic reaction) to abacavir and some do not. You must have a DOCUMENTED (medical or case management records) abacavir hypersensitivity reaction to participate in this trial.

 

Background

Approximately 5% of patients who take abacavir experience this reaction and symptoms can include rash, fever, fatigue, and malaise (generally ill feeling, among others). These symptoms generally occur during the first 6 weeks of treatment.
Objective
GlaxoSmithKline (the study sponsor) is looking at the genes, proteins and other blood factors that may be involved in the hypersensitivity reaction (serious allergy reaction). They will compare information from volunteers who experienced this reaction to information from individuals who did not. The long term objective is to develop a test that will predict abacavir sensitivity.

 

Study Design

This study does not involve a drug and only involves two clinic visits, blood draws, and a confidential interview. Volunteers will be compensated $50 for their inconvenience after both clinic visits are completed.
Inclusion
Criteria
  • HIV+ adult male or female
  • Documented abacavir hypersensitivity reaction (medical or case management records)

Status
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Enrolling
--

 

Volunteers will receive $50 compensation for their inconvenience
after both clinic visits are completed..

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, 2002.

 


 

 

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