Condition: Non-alcoholic Fatty Liver Disease · Sponsor: GlaxoSmithKline
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.
This description comes directly from the study's public registry record.
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| GSK Investigational Site | Rialto, California, United States | Recruiting |
| GSK Investigational Site | Tampa, Florida, United States | Recruiting |
| GSK Investigational Site | San Antonio, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07358546