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Evaluating the Pharmacokinetics and Safety of Miricorilant
RecruitingPhase 1
A Phase 1b, Open-Label Study Evaluating the Pharmacokinetics and Safety of Miricorilant in Adult Patients With Presumed Metabolic Dysfunction-Associated Steatohepatitis (MASH)
Who can join
Ages 18 to 75 · All sexes
Full eligibility criteria
Inclusion Criteria:
* Evidence of presumed MASH with either FibroScan liver stiffness measurement ≥ 8 kPa and controlled attenuation parameter (CAP) ≥ 280 dB/m OR historical biopsy within 12 months of screening that meets the following criteria:
1. Nonalcoholic fatty liver disease (NAFLD) activity score (NAS) ≥ 3 with at least ≥ 1 point in any two subcomponents of steatosis, inflammation, and ballooning, and a Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) fibrosis score of F1 OR
2. NAS ≥ 2 with at least ≥ 1 point in any two subcomponents of steatosis, inflammation, and ballooning, and a NASH CRN fibrosis score of F2 or 3.
* Aspartate aminotransferase (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.
* Presence of at least 1 of the following metabolic conditions that increase the risk of MASH:
1. Diagnosis of type 2 diabetes OR
2. Presence of 2 or more components of metabolic syndrome:
* Fasting blood glucose ≥ 100 mg/dL (5.6 mmol/L) or treatment for elevated blood glucose
* Systolic blood pressure ≥ 130 mm Hg, diastolic blood pressure ≥ 85 mm Hg, or treatment for hypertension
* Serum triglycerides ≥ 150 mg/dL (1.7 mmol/L) or drug treatment for elevated triglycerides
* Serum high-density lipoprotein (HDL) cholesterol \< 40 mg/dL (1 mmol/L) in men and \< 50 mg/dL (1.3 mmol/L) in women or drug treatment for low HDL
* Overweight or obese (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).
Exclusion Criteria:
* Women who are pregnant, planning to become pregnant, or are lactating.
* Have a BMI \< 18 kg/m2 or \> 45 kg/m2.
* Have significant alcohol consumption of more than 20 g per day for women and 30 g per day for men within 1 year prior to screening or score of ≥8 on AUDIT questionnaire
* Have had liver transplantation or plan to have liver transplantation during the study.
* Have type 1 diabetes.
* Have poorly controlled type 2 diabetes with a glycated hemoglobin (HbA1c)
* 9.5%.
* Have any other chronic liver disease
* History of cirrhosis or evidence of cirrhosis by clinical, imaging, or liver biopsy evaluation
* Have hepatic decompensation
Other exclusion criteria may applyAbout the study
A Phase 1b, Open-Label Study Evaluating the Pharmacokinetics and Safety of Miricorilant in Adult Patients With Presumed Metabolic Dysfunction-Associated Steatohepatitis (MASH)
What is being tested
- Miricorilant (drug)
Sponsor: Corcept Therapeutics · Participants: 15 · Started: Apr 30, 2026
Contact the study team
- Eric Lawitz, MD · Phone: 210-253-3426
- Toluwalase Okubote, MBBS, MPH, PMP · Phone: 210-253-3426
Official record on ClinicalTrials.gov — NCT07553663
Locations in the U.S.
| Texas | Site# 433, San Antonio |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.