Tipranavir Expanded Access Program (EAP) in PI-experienced Patients With HIV-1 Infection

NCT00097799 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2016-11-30

No results posted yet for this study

Summary

This study was designed to provide early access to and evaluate the safety of TPV/r in PI-experienced patients with HIV-1 infection.

Conditions

  • HIV Infections

Interventions

DRUG

Tipranavir

500 mg twice daily

DRUG

Ritonavir

200 mg twice daily

Sponsors & Collaborators

Principal Investigators

  • Boehringer Ingelheim · Boehringer Ingelheim

Eligibility

Sex
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-12-31
Primary Completion
2005-08-31

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 NCT00097799 on ClinicalTrials.gov