drugset / Trial / NCT07481734

Tesamorelin for Reduction of Liver Fat in Adults With Fatty Liver Disease (Mock Study)

NCT07481734

Phase 2 Recruiting 120 enrolled Hudson Biotech
RandomizedParallel-groupSingle-blindTreatment

Summary

This randomized, double-blind, placebo-controlled Phase II study evaluates whether daily subcutaneous tesamorelin (a growth hormone-releasing hormone analog) reduces liver fat in adults with fatty liver disease. Participants receive tesamorelin or matching placebo for 52 weeks, with standardized lifestyle counseling in both groups. Liver fat is quantified by MRI-proton density fat fraction (MRI-PDFF). Key safety monitoring includes glucose metrics and IGF-1.

Timeline

Start
2026-02-02
Primary completion
2027-02-14
Completion
2028-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Tesamorelin Peptide 2 mg Subcutaneous