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Clinical Trial Summary

This study will assess the effect of 3 doses of PXL065 versus placebo on liver fat content in NASH patients after 36 weeks of treatment


Clinical Trial Description

The study will be performed in patients with NASH. The primary endpoint will be the assessment of the change in the percentage of liver fat content (assessed by MRI-PDFF). ;


Study Design


Related Conditions & MeSH terms

  • Fatty Liver
  • NASH - Nonalcoholic Steatohepatitis
  • Non-alcoholic Fatty Liver Disease

NCT number NCT04321343
Study type Interventional
Source Poxel SA
Contact
Status Completed
Phase Phase 2
Start date September 1, 2020
Completion date June 20, 2022

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