drugset / Trial / NCT01668043

Study to Evaluate Safety and Efficacy of UB-421 Antibody in HIV-1 Infected Adults

NCT01668043 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this Phase IIa study is to determine whether the antibody (UB-421), targeting the HIV-1 receptor on the CD4 molecule of T-lymphocytes and monocytes, is safe and effective when multiple doses are administered by intravenous infusion to asymptomatic HIV-1 infected adults and to assess pharmacokinetic parameters of the antibody in blood and on cells. The neutralizing activity of UB-421 blocks HIV-1 from binding to its receptor on CD4-positive cells; thus, UB-421 functions as an immunotherapeutic intervention to prevent HIV-1 infection.

Timeline

Start
2012-09
Primary completion
2014-03
Completion
2014-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject SEMZUVOLIMAB Protein / enzyme biologic 10 mg/kg Intravenous
Subject SEMZUVOLIMAB Protein / enzyme biologic 25 mg/kg Intravenous

Indications

No indication recorded.