Phase 2 Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT07481734 Sponsor: Hudson Biotech Condition: Non-Alcoholic Fatty Liver Disease
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Phase 2 Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT07481734
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 and able to give your consent to participate
  • Imaging tests (such as an MRI) show that you have a significant amount of fat in your liver, consistent with a condition called MASLD or NAFLD
  • Tests suggest your liver scarring (fibrosis) is at an early stage — meaning you do not have advanced scarring (cirrhosis) or signs of serious liver complications
  • Your body weight has been fairly stable (within about 5%) for at least the last 3 months
  • If you take medications for diabetes, cholesterol, blood pressure, or weight loss, your doses have been unchanged for at least 3 months and are expected to stay the same throughout the study
  • You are willing and able to give yourself a daily injection under the skin, or have a caregiver who can do this for you
  • If you could become pregnant, you agree to use reliable birth control during the study and for 30 days after your last dose, and you have a negative pregnancy test at the start

Who may not be able to join:

  • You drink alcohol heavily on a regular basis (roughly more than one to two drinks per day, depending on your sex), enough to be causing liver damage
  • You have another ongoing liver condition, such as hepatitis B, hepatitis C, autoimmune hepatitis, or certain inherited liver diseases
  • You have been diagnosed with advanced liver scarring (cirrhosis) or serious liver failure
  • Your diabetes is poorly controlled, or you have an active, untreated eye condition related to diabetes (confirm with trial site)
  • You have used growth hormone or similar medications in the past 12 months
  • You regularly take steroid medications or certain other drugs known to cause or worsen liver damage (such as amiodarone, tamoxifen, or methotrexate)
  • You currently have cancer or are considered at high risk of cancer returning
  • You have a medical implant or other reason that makes having an MRI scan unsafe
  • You are currently pregnant or breastfeeding
  • You have a known allergy to the study drug (tesamorelin) or any of its ingredients, such as mannitol
  • You have had weight-loss (bariatric) surgery in the past 12 months, or you are planning to have it during the study

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 27 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

Phone: +86 13076790030

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
Sponsor
Hudson Biotech
Registry
ClinicalTrials.gov
Start date
2 February 2026
Est. completion
14 February 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Change from baseline in hepatic fat fraction by MRI-PDFF (percentage points)

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: 27 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