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Completed No phase listed Observational

HLA-B*5701 And Hypersensitivity To Abacavir

ClinicalTrials.gov ID: NCT00373945

Public ClinicalTrials.gov record NCT00373945. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 4:24 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Retrospective Case-Control Study to Estimate the Sensitivity and Specificity of a Pharmacogenetic Marker (HLA-B*5701) in Subjects With and Without Hypersensitivity to Abacavir.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This retrospective case-control study is being conducted to estimate the sensitivity of the pharmacogenetic marker, HLA-B\*5701 for hypersensitivity to abacavir (ABC HSR). The specificity of the marker, and its association with ABC HSR, as measured by odds ratios and 95% confidence intervals, will be evaluated as secondary endpoints. Cases will be defined in two ways - subjects who have clinically-suspected ABC HSR and a positive abacavir skin patch test reaction (CS-SPTPos) and subjects with clinically-suspected ABC HSR (CS-HSR), regardless of the results of skin patch testing. The study will include 40 CS-SPTPos Black cases matched with up to 200 abacavir-tolerant controls. In parallel, 40 CS-SPTPos White cases will be matched with up to 200 White controls. Some of the secondary analyses will use cases defined by clinical criteria alone (CS-HSR). Black and White subjects will be analyzed separately because of the differences in ABC HSR rates and in the carriage frequency of HLA-B\*5701.

Study identification

NCT ID
NCT00373945
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
280 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2006 (Type not available)
Primary completion
Not listed
Completion
Aug 2007 (Actual)
Last update posted
May 18, 2009

2006 – 2007

United States locations

U.S. sites
55
U.S. states
22
U.S. cities
44
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Little Rock Arkansas 72207 —
GSK Investigational Site Beverly Hills California 90210 —
GSK Investigational Site Loma Linda California 92357 —
GSK Investigational Site Los Angeles California 90027 —
GSK Investigational Site Los Angeles California 90069 —
GSK Investigational Site Newport Beach California 92663 —
GSK Investigational Site Oakland California 94609 —
GSK Investigational Site San Francisco California 94115-1931 —
GSK Investigational Site Tarzana California 91356 —
GSK Investigational Site Denver Colorado 80204 —
GSK Investigational Site Denver Colorado 80220 —
GSK Investigational Site Norwalk Connecticut 06851 —
GSK Investigational Site Fort Lauderdale Florida 33308 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Hollywood Florida 33020 —
GSK Investigational Site Orlando Florida 32803 —
GSK Investigational Site Orlando Florida 32812 —
GSK Investigational Site Atlanta Georgia 30308 —
GSK Investigational Site Atlanta Georgia 30309 —
GSK Investigational Site Atlanta Georgia 30339 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Chicago Illinois 60657 —
GSK Investigational Site Lexington Kentucky 40536 —
GSK Investigational Site Balitmore Maryland 21287 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Baltimore Maryland 21229-5299 —
GSK Investigational Site Springfield Massachusetts 01107 —
GSK Investigational Site Detroit Michigan 48201 —
GSK Investigational Site St Louis Missouri 63108 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Albany New York 12208 —
GSK Investigational Site Catskill New York 12414 —
GSK Investigational Site New York New York 10011 —
GSK Investigational Site Rochester New York 14604 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Valhalla New York 10595 —
GSK Investigational Site Chapel Hill North Carolina 27514 —
GSK Investigational Site Greenville North Carolina 27834 —
GSK Investigational Site Akron Ohio 44304 —
GSK Investigational Site Portland Oregon 97227 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77027 —
GSK Investigational Site Houston Texas 77098 —
GSK Investigational Site Longview Texas 75605 —
GSK Investigational Site Tyler Texas 75708 —
GSK Investigational Site Hampton Virginia 23666 —
GSK Investigational Site Seattle Washington 98122 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00373945, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 18, 2009 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00373945 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →