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Efficacy, Safety and Tolerability of VS-01 in Adult Patients With Acute-on-Chronic Liver Failure and Ascites (UNVEIL-IT)®

← catalyst calendar

NCT05900050 · results posted

Sponsored by Genfit (industry) · GNFT.PA — their whole pipeline →.

Phase
Phase 2
Status
Terminated
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
15actual
Sites
26
Countries
Belgium, France, Germany +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Sponsor Decision

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-07-02actualWhen the study began enrolling
Primary completion2025-10-15actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-10-15actualThe whole study's end, after follow-up
First posted2023-06-12actualWhen this record first appeared on the registry
Results posted2026-07-23actualWhen the sponsor posted results to the registry
Record updated2026-07-23actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Acute-On-Chronic Liver Failure
  • Ascites

Interventions

  • Drug: VS-01 on top of SOC
  • Other: SOC (Control Group)

Primary outcome

what the primary-completion date above is the date OF
Chronic Liver Failure Consortium (CLIF-C) ACLF Score at Day 7
measured Day 7

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2025-01-27 · 2.9 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-08-27 · 1.6 MB · SAP_001.pdf

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