A Study of Prevalence of the I50L Mutation When ATV Treated Patients Fail the Regimen

NCT00135447 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2011-04-14

No results posted yet for this study

Summary

The purpose of this study is to find out the frequency of the I50L substitution among patients experiencing treatment failure on an atazanavir-containing regimen.

Conditions

  • HIV Infections

Sponsors & Collaborators

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-09-30
Primary Completion
2009-09-30
Completion
2009-09-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00135447 on ClinicalTrials.gov