Recent Updates
Recently added Catalysts

NTZ on top of SOC

Phase 2

Acute Decompensation of Liver Cirrhosis | Small molecule | Gastrointestinal |Genfit SA Sponsored ADR|Last Updated: Jul 9, 2026

Target and mechanism

ModalitySmall molecule

Also known as NTZ 500mg BID on top of SOC

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment16

FDA Designations

No designations recorded

Clinical trial landscape

NTZ on top of SOC · 1 trial · 2 indications

Phase 2 1
NCT07694297Phase 2 Study of 500 mg BID NTZ on Top of Standard of Care in Patients With Acute Decompensation of Liver Cirrhosis at High Risk of Progression to Acute-on-Chronic Liver Failure or Established Acute-on-Chronic Liver FailureAcute Decompensation of Liver Cirrhosis
NOT YET_RECRUITING16 Analytics
PHASE2NOT YET_RECRUITING
Phase 2 Study of 500 mg BID NTZ on Top of Standard of Care in Patients With Acute Decompensation of Liver Cirrhosis at High Risk of Progression to Acute-on-Chronic Liver Failure or Established Acute-on-Chronic Liver Failure
Acute Decompensation of Liver CirrhosisUnlock trial analytics

Study Endpoints

Primary Endpoints

To evaluate the safety of 500 mg BID NTZ administered perorally
over 7 days on top of SOC follow-up period up to Day 28.

Safety defined as the incidence, relatedness, and severity (NCI-CTCAE v6.0 grade) of TEAEs including SAEs (comprising the evaluation of vital signs, ECGs, and laboratory parameters).

Unlock Study Endpoints

Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
NTZ 500mg BID on top of SOCEXPERIMENTALTreatment period NTZ 500mg BID on top of SOC during 7 days.

Interventions

NameTypeDescription
NTZ 500mg BID on top of SOCDRUGTreatment period NTZ 500mg BID on top of SOC
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to 74 Years
SexALL
Healthy VolunteersNo

Inclusion Criteria: Participants are eligible to be included in the study only if all of the following criteria apply: * Participants with liver cirrhosis of any underlying etiology (liver cirrhosis diagnosed by standard clinical criteria, imaging findings, and/or histology) * Recent acute clinica...

Unlock Eligibility Criteria

Recent Changes (Last 90 Days)

LOWJul 9, 2026NCT07694297NEW_TRIAL: changed
LOWJul 9, 2026NCT07694297NEW_TRIAL: changed

Frequently asked questions about NTZ on top of SOC

What is NTZ on top of SOC used for?

NTZ on top of SOC is an investigational small molecule being studied for the treatment of acute decompensation of liver cirrhosis, including patients at high risk of progression to acute-on-chronic liver failure or with established acute-on-chronic liver failure. It is administered at a dose of 500 mg twice daily in addition to standard of care.

Who makes NTZ on top of SOC?

NTZ on top of SOC is being developed by Genfit SA Sponsored ADR, which trades under the ticker GNFT. The company is conducting a Phase 2 clinical trial of this investigational therapy in patients with acute decompensation of liver cirrhosis.

What phase is NTZ on top of SOC in?

NTZ on top of SOC is in Phase 2 clinical development. It is an investigational drug and has not been approved by regulatory authorities. The ongoing Phase 2 study is designed to evaluate the therapy in patients with acute decompensation of liver cirrhosis at high risk of progression to acute-on-chronic liver failure.

What clinical trials is NTZ on top of SOC in?

NTZ on top of SOC is being evaluated in one Phase 2 clinical trial with the identifier NCT07694297. This study is not yet recruiting and plans to enroll 16 participants. The trial is uncontrolled, meaning there is no comparator arm, and it is open to adults aged 18 years and older.

Is NTZ on top of SOC the same as NTZ 500mg BID on top of SOC?

Yes, NTZ on top of SOC is also known as NTZ 500mg BID on top of SOC. The alternative name specifies the dosing regimen of 500 mg taken twice daily in addition to standard of care, as used in the Phase 2 clinical trial for acute decompensation of liver cirrhosis.