drugset / Trial / NCT05245292

Summary

The proposed study is a phase 1, open label, single arm study to evaluate the safety and antiretroviral activity of the combination of two long-acting broadly neutralizing antibodies, 3BNC117-LS dosed once at 30 mg/kg and 10-1074-LS dosed once at 10 mg/kg, both intravenously (IV) at week 0, plus an IL-15 superagonist complex, N-803, dosed at 6 mcg/kg, subcutaneously (SC) at week 1 and then every 3 weeks for a total of 8 doses, in ART-treated adults living with HIV during analytical treatment interruption.

Timeline

Start
2022-12-07
Primary completion
2025-12-09
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject N-803 Protein / enzyme biologic 6 ug/kg Subcutaneous
Subject Teropavimab Monoclonal antibody 30 mg/kg Intravenous
Subject Zinlirvimab Monoclonal antibody 10 mg/kg Intravenous