drugset / Trial / NCT07276204

Betaine vs. Placebo for Serologically Diagnosed Metabolic Dysfunction-associated Steatohepatitis (MASH)

NCT07276204

Phase 2 Not yet recruiting 70 enrolled Southern California Institute for Research and Education
RandomizedParallel-groupTriple-blindTreatment

Summary

The study will evaluate whether betaine reduces liver injury in people with metabolic dysfunction-associated steatohepatitis (MASH). MASH is a type of liver disease that occurs in some people with fatty liver. Betaine is a normal component in the human body and will be taken as a pill. Seventy (70) participants will be randomized to receive either betaine or placebo for 24 weeks. After stopping treatment, participants will be seen in clinic for another 24 weeks (total participation in the study is approximately 1 year). Procedures performed during the study include blood tests, MRI examinations, questionnaires, and clinic visits. We will measure improvement in liver injury with blood tests and with MRI.

Timeline

Start
2026-03-31
Primary completion
2029-12-31
Completion
2035-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Betaine Small molecule 1 g Oral