drugset / Trial / NCT04532294

Safety, Tolerability, Pharmacokinetics, and Immunogenicity of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2/COVID-19) Neutralizing Antibody in Healthy Participants

NCT04532294 ↗

Phase 1 Completed 18 enrolled BeiGene
RandomizedParallel-groupTriple-blindBasic science

Summary

The primary purpose of this study is to investigate the safety and tolerability of BGB-DXP593 administered intravenously as a single dose in healthy participants

Timeline

Start
2020-09-08
Primary completion
2021-02-13
Completion
2021-02-13

Drugs

EvaluationDrugModalityDoseRoute
Subject BGB-DXP593 Monoclonal antibody 10 mg/kg Intravenous
Subject BGB-DXP593 Monoclonal antibody 30 mg/kg Intravenous

Indications