drugset / Trial / NCT04250636

Summary

The proposed study is a phase 1, open label, single arm study to evaluate the safety, pharmacokinetics and antiviral activity of single intravenous infusions of 3BNC117-LS and 10-1074-LS, each monoclonal antibody (mAb) dosed at 30 mg/kg in viremic human immunodeficiency virus (HIV)-infected individuals.

Timeline

Start
2020-10-13
Primary completion
2022-01-21
Completion
2022-02-11

Drugs

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