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Clinical Trial Summary

A Phase 2, multi-center, randomized, controlled, open-label study to evaluate the effects of the intraperitoneal, liposomal formulation VS-01 in patients with an acute episode of hepatic and/or extrahepatic organ dysfunctions and failures in the presence of liver cirrhosis (Acute-on-Chronic Liver Failure, ACLF) and accumulation of fluid in the abdominal cavity (ascites)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05900050
Study type Interventional
Source Genfit
Contact Versantis AG, Katharina Staufer, MD
Phone +333 20 16 40 00
Email clinical@versantis.com
Status Recruiting
Phase Phase 2
Start date July 2, 2023
Completion date June 2025

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