Overview

A Study of Efimosfermin Alfa in Adults With Hepatic Impairment

Status:
NOT_YET_RECRUITING
Trial end date:
2027-09-01
Target enrollment:
Participant gender:
Summary
This study is designed to study the pharmacokinetic (PK) and safety profiles of a single dose of efimosfermin alfa in participants with varying degrees of Hepatic Impairment (HI) (assessed by Child-Pugh score) due to steatotic liver disease, with and without significant alcohol consumption.
Phase:
PHASE1
Details
Lead Sponsor:
GlaxoSmithKline