drugset / Trial / NCT05573204

Comparative Study Between Obeticholic Acid Versus Vitamin E in Patients with Non-alcoholic Steatohepatitis

NCT05573204

Phase 2 Active not recruiting 59 enrolled Tanta University
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims at evaluating and comparing the protective outcomes of using Obeticholic acid versus Vitamin E in NASH patients without cirrhosis. The intervention is 6-months duration and the study will assess the efficacy of either drug as fibrosis improvement (≥ 1 stage) with no worsening of NASH or NASH resolution with no worsening of fibrosis with the study considered successful if either 1ry end point is met. . Also, assessment of biochemical markers related to steatosis, inflammation, oxidative stress, insulin resistance and liver fibrosis will be done.

Timeline

Start
2021-09-01
Primary completion
2026-10-25
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Obeticholic Acid Small molecule 10 mg Oral
Comparator Vitamin E Other / unclassified 400 mg