Oral anticoagulation (apixaban) to prevent early liver disease worsening

APEACH: Apixaban to Prevent dEcompensation of eArly liver CirrHosis trial

Registry ID
ISRCTN11391276
Source registry
ISRCTN
Status
Recruiting
Phase
PHASE3
Study type
INTERVENTIONAL
Sponsor
University College London
Enrollment
1142
Start date
2026-06-30
Completion date
2030-11-30
Last update
2026-08-17

Conditions

Summary

Liver cirrhosis secondary to alcohol, with or without associated metabolic risk factors, i.e. Alcohol Related Liver Disease (ARLD) or metabolic dysfunction-associated steatotic liver disease, where there has been a significant history of alcohol consumption (MetALD)

Detailed description

1. Apixaban 2.5mg film-coated tablets (licenced in the UK and/or approved country) 2. Placebo to match film-coated tablets (same visual appearance, no active ingredients). Participants will be instructed to take one tablet of 2.5mg / matched placebo twice a day (morning and evening). The treatment period will be for a minimum of 12 months for the final randomised participant, and a maximum of 49 months for the first randomised participant. Medication can be taken with or without food.

Interventions

Inclusion criteria

1. Liver cirrhosis secondary to alcohol, with or without associated metabolic risk factors, i.e. Alcohol related liver disease (ARLD) or metabolic dysfunction-associated steatotic liver disease, where there has been a significant history of alcohol consumption (MetALD) 2. Cirrhosis will be based on histology, or clear radiological evidence, e.g. nodular or heterogeneous liver or non-invasive testing (e.g. Fibroscan®, or Enhanced Liver Fibrosis (ELF) test 3. Childs A Cirrhosis (Participants with a previous episode of decompensated cirrhosis who have now recompensated can be included) 4. Participants with no hepatic encephalopathy or low-grade hepatic encephalopathy (Grade 0 or 1) taking lactulose and/or rifaximin 5. Aged ≥18 years 6. Clinical evidence of portal hypertension, defined as any 1 of: 6.1. Evidence of abdominal collateral circulation, recanalised umbilical vein or varices on imaging 6.2. Asymptomatic ascites (trace only) seen around the liver on imaging in patients who are not taking diuretics 6.3. Liver stiffness measurement >20kPa on FibroScan®/ Vibration-Controlled Transient Elastography (VCTE) (where BMI <35) 6.4. Presence of Gastro-oesophageal varices at endoscopy 6.5. Hepatic venous pressure gradient ≥ 10mmHg Or Platelet count < 150,000 µL AND any 1 of: 6.6. Spleen size >13 cm in length 6.7. Liver stiffness measurement >20kPa on FibroScan®/VCTE (where BMI >35) 6.8. Presence of portal hypertensive gastropathy at endoscopy

Exclusion criteria

1. Evidence of decompensation (e.g. ascites requiring treatment other than a thin rim around the liver on imaging). (Evidence of decompensation as follows: Grade 2 or 3 Ascites, Grade 2 – 4 Hepatic Encephalopathy, Variceal Haemorrhage). 2. Causes for cirrhosis other than alcohol, including those with MASLD who have never drunk alcohol above government recommended levels (14 units/week) 3. Pre-existing splanchnic vein thrombosis (portal, splenic, mesenteric, and hepatic veins) 4. Use of (and need for) anticoagulation or dual antiplatelet therapy or clopidogrel 5. Platelets <50x109/L1 at screening 6. Moderate-severe renal impairment defined as eGFR <30ml/min at screening 7. Recent variceal bleed or untreated large varices 8. Malignancy in the last 2 years, if unlikely to survive trial because of comorbidity in the location, according to the PI’s opinion 9. Hepatocellular carcinoma 10. Severe cardiac failure or Chronic Obstructive Pulmonary Disease (COPD) 11. Pregnancy 12. INR >1.7 (after vitamin K correction) at screening 13. Previous hypersensitivity reaction to apixaban

Locations

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