drugset / Trial / NCT03526848

Summary

The proposed study is a phase 1, open label, randomized study to evaluate the safety and antiretroviral activity of seven infusions of 3BNC117 and 10-1074, administered intravenously at 30 mg/kg dose level, in human immunodeficiency virus (HIV)-infected individuals on combination antiretroviral therapy (ART) and during an analytical interruption of ART.

Timeline

Start
2018-06-05
Primary completion
2021-09-30
Completion
2022-02-11

Drugs

EvaluationDrugModalityDoseRoute
Subject LAFUVITUG Monoclonal antibody 30 mg/kg Intravenous
Subject Zinlirvimab Monoclonal antibody 30 mg/kg Intravenous