A Study of Efimosfermin Alfa for MASH Cirrhosis
This study is testing a drug called efimosfermin in people with metabolic dysfunction-associated steatohepatitis (MASH) and compensated cirrhosis (scarring of the liver that is stable). You would receive either efimosfermin or a placebo (an inactive substance) through injections under the skin. Researchers want to see if efimosfermin is safe, how well your body handles it, and if it shows early signs of working. They are also looking at how the drug moves through your body. To join, you need to be between 18 and 75 years old, have a history of at least two metabolic syndrome components, and a liver biopsy confirming MASH with F4 fibrosis (the most severe stage of scarring). The main goal is to track any side effects you might experience over about 100 weeks.
- Study design
- This is an interventional study planning to enroll 42 participants. It compares efimosfermin to a placebo.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be monitored for treatment-related side effects for up to 100 weeks.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study of Efimosfermin Alfa in Participants With Biopsy-confirmed Cirrhosis (Compensated) Due to MASH
At a glance
Conditions
NCT06920043
Where you'd take part
This study runs at 30 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
GSK Investigational Site
Chandler, Arizonastudy coordinator listed
Recruiting
GSK Investigational Site
Mesa, Arizonastudy coordinator listed
Recruiting
GSK Investigational Site
Tucson, Arizonastudy coordinator listed
Recruiting
GSK Investigational Site
Fresno, Californiastudy coordinator listed
Recruiting
GSK Investigational Site
Lancaster, Californiastudy coordinator listed
Recruiting
GSK Investigational Site
Pasadena, Californiastudy coordinator listed
Recruiting
GSK Investigational Site
Rialto, Californiastudy coordinator listed
Recruiting
GSK Investigational Site
Santa Maria, Californiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- Number of participants with treatment emergent adverse events (TEAEs)From Day 1 to 100 weeks
To assess the effects of efimosfermin on safety and tolerability.