drugset / Trial / NCT00385567

A Trial of PEHRG214 in HIV-Infected Patients

NCT00385567 ↗

Phase 2 Terminated 70 enrolled Virionyx Corporation Limited
RandomizedParallel-groupOpen-labelTreatment

Summary

HRG2 is a Phase 2 randomized, controlled, open-label, multi-dose trial to determine the efficacy, safety, immunogenicity, and pharmacokinetic profile of PEHRG214 in HIV-infected patients, treated three times weekly for up to 16 weeks. All patients are receiving optimized standard of care HAART. The primary objective of the study is to determine the effect of PEHRG214 in decreasing the viral load (\>=1.0 log10), as compared to a Control group. The primary hypothesis is that treatment with PEHRG214 will result in clinically meaningful and sustained viral load suppression. The total sample size is 70-74 patients from approximately 8-10 participating study centers. The first 16-20 patients are enrolled in the non-randomized "pilot arm" and 54 subsequent patients are randomized (2:1 within center) to Treatment or Control group. The total study duration is 7-12 months.

Timeline

Start
2007-01
Primary completion
2008-09
Completion
2008-09

Outcome

Outcome not reported

Stopped (Enrollment): “Difficulty recruiting eligible patients in timely fashion”

Drugs

EvaluationDrugModalityDoseRoute
Subject PEHRG214 Unknown 2 mg/kg Intravenous
Subject PEHRG214 Unknown 4 mg/kg Intravenous
Subject PEHRG214 Unknown 8 mg/kg Intravenous