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Study identifier: NCT06920043 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study of Efimosfermin Alfa in Participants With Biopsy-confirmed Cirrhosis (Compensated) Due to MASH

Condition: Metabolic Dysfunction-Associated Steatohepatitis · Non-alcoholic Fatty Liver Disease  ·  Sponsor: GlaxoSmithKline

PhasePhase 2
Planned participants42
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the safety, tolerability, preliminary efficacy, and pharmacokinetics (PK) of efimosfermin in participants with metabolic dysfunction associated steatohepatitis (MASH) and compensated cirrhosis consistent with stage F4 fibrosis.

This description comes directly from the study's public registry record.

Talk to the study team

US GSK Clinical Trials Call Center  ·  877-379-3718  ·  GSKClinicalSupportHD@gsk.com

EU GSK Clinical Trials Call Center  ·  +44 (0) 20 89904466  ·  GSKClinicalSupportHD@gsk.com

Always discuss trial participation with your own doctor first.

Locations (30)

GSK Investigational SiteChandler, Arizona, United StatesRecruiting
GSK Investigational SiteMesa, Arizona, United StatesRecruiting
GSK Investigational SiteTucson, Arizona, United StatesRecruiting
GSK Investigational SiteFresno, California, United StatesRecruiting
GSK Investigational SiteLancaster, California, United StatesRecruiting
GSK Investigational SitePasadena, California, United StatesRecruiting
GSK Investigational SiteRialto, California, United StatesRecruiting
GSK Investigational SiteSanta Maria, California, United StatesRecruiting
GSK Investigational SiteMiami, Florida, United StatesRecruiting
GSK Investigational SiteViera, Florida, United StatesRecruiting
GSK Investigational SiteMarietta, Georgia, United StatesRecruiting
GSK Investigational SiteBaltimore, Maryland, United StatesRecruiting

+ 18 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06920043