Blood thinner may stop early cirrhosis from turning deadly — a major trial puts it to the test
NCT ID NCT07726693
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
Liver disease is the only major cause of death on the rise, and once cirrhosis develops, no proven medications exist to help people live longer. This trial tests whether apixaban, a blood thinner already used for clots, can prevent early-stage cirrhosis from progressing to a dangerous 'decompensated' state that causes severe symptoms and shortens life. Over 1,100 participants with compensated cirrhosis will take either apixaban or a placebo for up to four years to see if the drug delays or prevents liver-related hospitalizations and death.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a blood-thinning drug called apixaban (2.5 mg twice daily)
- What this could lead to
- If it works, this could offer the first medication proven to help people with early cirrhosis live longer without severe liver complications.
- What could go wrong
- This is a large trial, but earlier smaller studies were not conclusive. Apixaban increases bleeding risk, which could be dangerous in some patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 1,142 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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: * Evidence of abdominal collateral circulation, recanalised umbilical vein or varices on imaging * Asymptomatic ascites (trace only) seen around the liver on imaging in patients who are not taking diuretics * Liver stiffness measurement \>20kPa on FibroScan®/ Vibration- Controlled Transient Elastography (VCTE) (where BMI \<35) * Presence of Gastro-oesophageal varices at endoscopy * Hepatic venous pressure gradient ≥ 10mmHg Or Platelet count \< 150,000 μL AND any 1 of: * Spleen size \>13 cm in length * Liver stiffness measurement \>20kPa on FibroScan®/VCTE (where BMI \>35) * Presence of portal hypertensive gastropathy at endoscopy Exclusion Criteria: 1. Evidence of decompensation (e.g. ascites requiring treatment other than a thin rim around liver on imaging, as above) (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/L 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 last 2 years if unlikely to survive trial because of comorbidity in the location PI's opinion 9. Hepatocellular carcinoma 10. Severe cardiac failure1 or Chronic Obstructive Pulmonary Disease (COPD) 11. Pregnancy 12. INR \>1.7 (After vitamin K correction) at screening 13. Previous hypersensitivity reaction to Apixaban
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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