A-TANGO Phase 2 Study

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorYaqrit Ltd

About this trial

The purpose of this research is to know if a new combination of drugs (TAK-242 and G-CSF) in combination with standard therapy for acute-on-chronic liver failure (ACLF) is more effective than standard therapy for ACLF treatment and is safe.

Description of the population to be studied: ACLF is a syndrome that occurs in patients with chronic liver disease, with or without previously diagnosed cirrhosis, which is characterized by acute hepatic decompensation. Cirrhosis is a chronic disease of the liver marked by degeneration of cells, inflammation, and thickening and scarring (fibrosis) of liver tissue. Hepatic decompensation is a sudden decline in liver function. It is characterized by severe liver damage and complications like jaundice (yellowing of the skin or whites of the eyes), ascites (a condition where excess fluid accumulates in the abdominal cavity and in abdominal organs) and encephalopathy (a group of symptoms that result from damage or dysfunction in the brain, causing a range of cognitive and neurological impairments). It may result in liver failure, one or more organ failures other than liver (renal, brain, coagulation, respiratory, cardiovascular), and is associated with increased mortality within 28-days and up to 3 months from onset. Grade 1 ACLF has a \>15% risk of mortality at 28 days.

Purpose of the study: The investigational medication, TAK-242, is aimed at stopping an "over-reaction" of the immune system (the body's defense system) while G-CSF encourages your liver cells to grow. In patients with severe inflammation of the liver due to alcohol \[severe alcoholic hepatitis (sAH)\] and ACLF, this over-reaction may cause the liver and other organs in the body to suddenly stop working (organ failure). The hypothesis of the study is that by blocking this over-reaction and encouraging your liver cells to grow your condition may improve.

Eligibility criteria

Qualifiers

Male and female subjects ≥18 of age and ≤75 years of age

Compliance with acceptable contraceptive methods.

With a diagnosis of severe alcoholic hepatitis that is resistant to steroid therapy as defined by a Lille score of >0.45 and/or in whom steroids are contraindicated.

Eligible subjects will have Grade 1-3 ACLF with a maximum of three organ failures using the CLIF-C OF score AND the CLIF-C ACLF-CRP score of >35 and <60.

Disqualifiers

Refusal to give informed consent

Mechanical ventilation due to respiratory failure and/or need for renal replacement therapy and or requiring inotropes for circulatory support with a noradrenaline requirement of >0.5ug/kg/min to maintain mean arterial pressure > 70mmHg

Subject has received any investigational drug within 30 days of randomization

history of liver transplantation

Trial design

Treatments tested in this trial

  • Placebo
  • TAK-242
  • G-CSF (Filgrastim)

Treatment groups

78 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Yaqrit Ltd

Lead sponsor

European Foundation for Study of Chronic Liver Failure

Collaborator

University College, London

Collaborator

HEPYX LIMITED

Collaborator

CROWDHELIX LIMITED

Collaborator

Charite University, Berlin, Germany

Collaborator

University of Leipzig

Collaborator

Concentris research management gmbh

Collaborator

Assistance Publique - Hôpitaux de Paris

Collaborator

Leiden University Medical Center

Collaborator

INTERNATIONAL MARKET ACCESS CONSULTING GMBH

Collaborator

KlinEra Global Services

Collaborator

European Association for the Study of the Liver

Collaborator

EUROPEAN LIVER PATIENTS' ASSOCIATION

Collaborator