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Clinical Trial Summary

In this study, a single dose of VIR-2218 up to 200 mg SC or VIR-3434 at 300 mg SC monotherapy or a combination of VIR-2218 and VIR-3434 will be administered to assess the pharmacokinetic (PK) exposure, safety, and tolerability of VIR-2218 and VIR-3434 in participants with cirrhosis and Hepatic Impairment, defined using the Child-Pugh-Turcotte (CPT) categorization.


Clinical Trial Description

Participants may be enrolled in Cohorts 1, 2, 3, 4, 5, 6, 7, 8, and 9 in a non-randomized way. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05484206
Study type Interventional
Source Vir Biotechnology, Inc.
Contact
Status Recruiting
Phase Phase 1
Start date September 21, 2022
Completion date April 30, 2027

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