drugset / Trial / NCT01208649

Effects of Exenatide (Byetta®) on Liver Function in Patients With Nonalcoholic Steatohepatitis (NASH)

NCT01208649

Phase 4 Completed 13 enrolled Ruhr University of Bochum
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective is to test the hypothesis that 24 weeks of treatment with exenatide will improve the histological acitvity of NASH (steatosis,necroinflammation, ballooning), summarized in the recently introduced NASH-score in patients with normal, impaired or diabetic glucose tolerance compared to dietary guidance alone.

Timeline

Start
2008-07
Primary completion
2010-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Exenatide Peptide 10 ug Subcutaneous

Indications