There is one clinical trial.
This is a phase 1 study in which healthy adult volunteers will receive BRII-198 or placebo
and will be assessed for safety, tolerability, and pharmacokinetics.
Primary Outcomes
Measure: Incidence of adverse events (AEs) by CTCAE v5.0 Time: up to 24 weeks
Measure: Proportion of subjects with SAEs Time: up to 24 weeks
Measure: Proportion of subjects with infusion-related reactions Time: up to 24 weeks
Measure: Proportion of subjects with hypersensitivity reactions Time: up to 24 weeks
Secondary Outcomes
Measure: Serum Concentration of BRII-198 Time: up to 24 weeks