The purpose of this study is to assess the impact of prospective drug level monitoring and dose-adjustment of nelfinavir (NFV) on the clinical and virologic outcomes in a group of HIV-infected patients who have achieved virologic success while receiving a nelfinavir containing highly active antiretroviral therapy (HAART) regimen.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
University of Wisconsin Hospital and Clinics
Madison, Wisconsin, United States
Virologic response
Nelfinavir pharmacokinetics
Impact of nelfinavir and M8 pharmacokinetics on virologic response
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