NCT Number: NCT00240552
Fosamprenavir Expanded Access
This open-label study will enable HIV-infected adults with limited treatment options to receive fosamprenavir until commercial supplies are available in Switzerland.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
GSK Investigational Site, Aarau, Switzerland
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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.
Treatment and study plan
Telzir®
DrugOther names: fosamprenavir
Sponsors and collaborators
Lead sponsor
ViiV Healthcare
Industry
Collaborators
- GlaxoSmithKline
Registry information
Official study title
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
Important dates
- Study start
- 2003
- Study completion
- 2005
- First posted
- Oct 18, 2005
- Registry last updated
- Sep 12, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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