Phase 2 Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT05424003 Sponsor: University of Virginia Condition: Non-Alcoholic Fatty Liver Disease
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Phase 2 Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT05424003
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 18 and 75 years old (male or female) and have had a liver transplant for any reason (such as fatty liver disease, hepatitis C, alcohol-related liver disease, or autoimmune hepatitis)
  • Your liver transplant surgery took place between 8 and 24 weeks before joining the study
  • You have been diagnosed with diabetes, pre-diabetes, or have a fasting blood sugar level above 125 mg/dL
  • You are able to understand and sign a consent form agreeing to take part in the study
  • You have already been discharged from the hospital after your liver transplant
  • You are able to eat and tolerate a normal diet
  • Your transplanted liver is working normally, as confirmed by your liver doctor or surgeon
  • You are on a stable anti-rejection medication routine as set by Virginia Commonwealth University's transplant program (typically two specific types of anti-rejection drugs)
  • If you are a woman who could become pregnant, you must not currently be pregnant (confirmed by a negative pregnancy test), not be breastfeeding, and must be using an accepted form of birth control, or be surgically sterile or post-menopausal

Who may not be able to join:

  • Your Body Mass Index (BMI — a measure of body weight relative to height) is 27 or below
  • Your kidneys are not filtering blood well enough (confirm with trial site)
  • You have Type 1 autoimmune diabetes, confirmed by a specific blood test or a history of a serious diabetes-related emergency called ketoacidosis
  • You have a history of gastroparesis (a condition where the stomach empties food too slowly)
  • You or a close family member have had a specific type of thyroid cancer (medullary thyroid cancer) or a related hormonal condition called Multiple Endocrine Neoplasia type 2
  • You have a history of pancreatitis (inflammation of the pancreas)
  • You have had an active cancer since your liver transplant, with the exception of certain common, less dangerous skin cancers
  • You have a history of uncontrolled or unstable damage to the eyes caused by diabetes
  • You are currently experiencing rejection of your transplanted liver
  • You have a blockage or clot in the main artery supplying your transplanted liver
  • You have a history of not following your medical treatment plan as directed
  • You are currently taking a type of diabetes medication known as a GLP-1 receptor agonist or an SGLT-2 inhibitor at the time of screening (confirm with trial site)
  • You have had an allergic reaction to semaglutide or any of its ingredients in the past
  • You are pregnant, breastfeeding, planning to become pregnant during the study, or not using adequate contraception

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Mohammad S Siddiqui, MD, Virginia Commonwealth University

Phone: 804-828-5434

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
22 February 2024
Est. completion
1 August 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in weight

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov