A Trial of Observed Long-acting, Anti-HIV Treatment With a Monoclonal CCR5 Antibody (PRO 140) as an Adjunct to a New, Optimized, Oral Antiretroviral Regimen in HIV-infected Injection Drug Users With Viral Rebound and Documented Poor Adherence
Withdrawn before enrolling · Phase 2 · Has a placebo group
Conditions studied: HIV
In brief
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.
Key facts
- Study ID
- NCT01272258
- Run by
- CytoDyn, Inc.
- People needed
- 0
- Starts
- 2013-12-01
- Expected to finish
- 2017-02-01
- Last updated by the study team
- 2017-02-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Drexel University College of Medicine — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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