PRO 140 2102 is a phase 2b, national, multicenter, randomized, double-blind, placebo-controlled study in order to evaluate the safety and efficacy of PRO 140 (anti-CCR5 monoclonal antibody) administered subcutaneously as an adjunct to a new, optimized, oral antiretroviral regimen in HIV-infected injection drug users with viral rebound and documented poor adherence to the previous antiretroviral regimen.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Drexel University College of Medicine
Philadelphia, Pennsylvania, United States
Specific measure that will be used to determine the effect of the interventions: Percentage of subjects without virologic failure at week 24.
Percentage of subjects without virologic failure at week 24.
Time frame: 24 Weeks
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