Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Neutralizing Antibody BGB-DXP593 in Participants With Mild-to-Moderate Coronavirus Disease 2019 (COVID-19)

Completed · Phase 2 · Has a placebo group

Conditions studied: Covid19

In brief

The primary objective of this study is to evaluate the efficacy of BGB-DXP593 administered intravenously as a single dose in participants with mild to moderate COVID-19

Key facts

Study ID
NCT04551898
Run by
BeiGene
People needed
181
Starts
2020-12-02
Expected to finish
2021-05-25
Last updated by the study team
2024-10-26

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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