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

PHASE1CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

September 8, 2020

Primary Completion Date

February 13, 2021

Study Completion Date

February 13, 2021

Conditions
Covid19
Interventions
DRUG

BGB DXP593

Administered intravenously (IV) as specified in the treatment arm

DRUG

Placebo

Placebo to match BGB-DXP593

Trial Locations (1)

4006

Q PHARM, Herston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

BeiGene

INDUSTRY