Skip to main content
Clinical Trials/NCT00240552
NCT00240552
Completed
Phase 4

An Open-label Phase III Study to Provide Access to Fosamprenavir and to Assess the Long Term Safety and Tolerability of Fosamprenavir Containing Regimens in HIV Infected Patients With Limited Treatment Options

ViiV Healthcare1 site in 1 country85 target enrollmentJuly 2003

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Infection, Human Immunodeficiency Virus
Sponsor
ViiV Healthcare
Enrollment
85
Locations
1
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This open-label study will enable HIV-infected adults with limited treatment options to receive fosamprenavir until commercial supplies are available in Switzerland.

Registry
clinicaltrials.gov
Start Date
July 2003
End Date
August 2005
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • HIV-1 infected subjects.
  • Subjects must belong to one of the following populations:
  • Subjects with limited treatment options due to viral resistance, interactions, or tolerability issues with other antiretroviral drugs.
  • Subjects who already receive amprenavir (Agenerase®)
  • Subjects for whom once daily dosing of antiretroviral therapy is indicated, including, once daily dosing with fosamprenavir/ritonavir.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

Loading locations...

Similar Trials