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NCT06947304CompletedPhase 1

Evaluation of Miricorilant on Liver Fat in Patients With MASLD

A Phase 1, Open-Label Study Evaluating the Effect of Miricorilant on Hepatic Lipids in Patients With Presumed Metabolic Dysfunction-Associated Steatohepatitis (MASH)

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

A Phase 1, Open-Label Study Evaluating the Effect of Miricorilant on Hepatic Lipids in Patients with Presumed Metabolic Dysfunction-Associated Steatohepatitis (MASH)

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
9 (actual)
First submitted
21 Apr 2025
Start date
22 Aug 2025
Primary completion date
13 Aug 2026
Lead sponsor
Corcept Therapeutics
NCT number
NCT06947304

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 9
  • From 22 Aug 2025 to the primary completion date, 13 Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Significant alcohol consumption exceeding 20 g/day for women or 30 g/day for men within 1 year prior to screening.
  • Positive urine drug screen for amphetamines, cocaine, opiates, or cannabinoids.
  • History of myocardial infarction, unstable angina, or stroke within 3 months prior to screening.
  • Current use of medications prohibited due to potential drug-drug interactions with study treatment.

Other illness

  • Other chronic liver diseases such as hepatitis B or C, autoimmune hepatitis, primary biliary cholangitis, or Wilson's disease.
  • Uncontrolled hypertension (systolic \> 160 mm Hg or diastolic \> 100 mm Hg).

Other

  • Participation in another clinical trial for MASH or weight loss (e.g., GLP-1 receptor agonists) within the last 3 months.
  • Participation in any other clinical trial within the last 3 months or 5 half-lives of the treatment, whichever is longer.
  • Women who are pregnant, planning to become pregnant, or lactating.
  • BMI \< 18 kg/m² or \> 45 kg/m².
  • Known or suspected cirrhosis or signs of hepatic decompensation.
  • Contraindications to magnetic resonance imaging (MRI).
    • Other exclusion criteria may apply

Who the study is looking for

  • AST \> 17 U/L for women and AST \> 20 U/L for men. The AST inclusion criterion does not apply to participants with an eligible historical liver biopsy performed within 12 months of screening showing one of the following:
    • NAFLD Activity Score (NAS) ≥ 4 (with at least 1 point in each subcomponent of steatosis, inflammation, and ballooning) and NASH Clinical Research Network (CRN) fibrosis score of F0 OR
    • NAS ≥ 3 (with at least 1 point in each subcomponent of steatosis, inflammation, and ballooning) and NASH CRN fibrosis score of F1 OR
    • NAS ≥ 2 (with at least 1 point in subcomponent of ballooning or inflammation) and a NASH CRN fibrosis score of F2-3
  • MRI-PDFF with ≥ 8% steatosis; this assessment must be performed within 4 weeks of the Baseline Visit.
  • Presence of at least 1 of the following metabolic syndrome characteristics that increase the risk of MASH:
    • Diagnosis of type 2 diabetes managed with diet alone or diet and metformin (metformin dose must be stable for at least 1 month prior to screening) OR b. Presence of 3 or more components of metabolic syndrome: i. Fasting blood glucose ≥ 100 mg/dL (5.6 mmol/L) or treatment for elevated blood glucose with metformin ii. Systolic blood pressure ≥ 130 mm Hg, diastolic blood pressure ≥ 85 mm Hg, or treatment for hypertension iii. Serum TG ≥ 150 mg/dL (1.7 mmol/L) iv. Serum high-density lipoprotein cholesterol (HDL) \< 40 mg/dL (1 mmol/L) in men and \< 50 mg/dL (1.3 mmol/L) in women or drug treatment for low HDL v. Having overweight or obesity (body mass index \[BMI\] ≥ 25 kg/m2 \[BMI
    • 23 kg/m2 in Asians\]), or increased waist circumference ≥ 102 cm (40 in) in men and ≥ 88 cm (35 in) in women (men ≥ 90 cm \[35.4 in\]; women ≥ 80 cm \[31.5 in\] in Asians).
    • Other inclusion criteria may apply

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Missouri
Coordinator of this site? Confirm its status
ColumbiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.