Nonalcoholic Steatohepatitis (NASH)

5

Review clinical trials related to Nonalcoholic Steatohepatitis (NASH). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluating the Pharmacokinetics and Safety of Miricorilant

A Phase 1b, Open-Label Study Evaluating the Pharmacokinetics and Safety of Miricorilant in Adult Patients With Presumed Metabolic Dysfunction-Associated Steatohepatitis (MASH)

Participants needed: 15
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Corcept TherapeuticsUpdated: May 26, 2026Locations: 1
Eligibility criteria

Nonalcoholic fatty liver disease (NAFLD) activity score (NAS) ≥ 3 with at least... [+8]

Women who are pregnant, planning to become pregnant, or are lactating. [+9]

Status: Recruiting

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)

Participants needed: 8
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Corcept TherapeuticsUpdated: Feb 11, 2026Locations: 1
Eligibility criteria

NAFLD Activity Score (NAS) ≥ 4 (with at least 1 point in each subcomponent of st... [+4]

Participation in another clinical trial for MASH or weight loss (e.g., GLP-1 rec... [+11]

Status: Recruiting

Study of ADI-PEG 20 Versus Placebo in Subjects With NASH

Evaluate efficacy and safety of ADI-PEG 20 in patients with NASH

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: Polaris GroupUpdated: Sep 23, 2025Locations: 10
Eligibility criteria

Males and non-lactating, pregnancy test negative females between 18 - 80 years o... [+22]

Weight gain or loss > 5% in the 3 months prior to randomization or > 10% in the... [+18]

Status: Recruiting

To Evaluate the Safety, Tolerability, Pharmacokinetics and Food Effects of IMM-H014 in Healthy Subjects

This study will evaluate the safety, tolerability and pharmacokinetics (PK) of escalating single- and multiple-oral doses of IMM-H014 on fasted condition, and characterize PK of IMM-H014 on an empty stomach (fasted condition) and following a high fat, high calorie meal (fed condition) in a 2-period, 2-sequence manner. The study will be conducted in 3 parts (Ascending single dose, multiple dose and food effect). Participants will receive either IMM-H014 or placebo.

Participants needed: 138
Trial details
Phase: Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: Changchun Intellicrown Pharmaceutical Co. LTDUpdated: Apr 11, 2025Locations: 1
Eligibility criteria

Subjects can voluntarily participate in the clinical trial, sign informed consen... [+3]

Clinical history of drug allergy or specific allergic diseases (asthma, urticari... [+21]

Status: Recruiting

Quantitative Ultrasound Techniques for Diagnosis of Nonalcoholic Steatohepatitis

Nonalcoholic fatty liver disease is the most common liver disease in Western countries, due in large part to its association with type 2 diabetes and obesity. The more advanced form of this disease is known as nonalcoholic steatohepatitis (NASH). If left untreated, NASH can evolve to cirrhosis, the late stage of fibrosis. Once cirrhosis is established, patients are at increased risk of developing gastrointestinal bleeding, liver cancer and liver failure that may require transplantation. A liver biopsy is currently needed to diagnose the severity of fatty liver disease but this is usually not indicated in asymptomatic patients. This procedure requires the insertion of a needle inside the liver to remove a small piece of tissue for examination under microscope. Liver biopsy is an invasive procedure with a small risk of major complications such as bleeding in 0.5% of cases. It is also affected by sub-optimal sampling leading to diagnostic errors Ultrasound is optimum for screening patients with or without symptoms because it is a safe and widely available technology to scan the whole liver. Members of our team have developed Advanced ultrasound techniques that provide unique information not possible with state-of-the-art techniques. Unlike liver biopsy, these techniques would be applicable even in asymptomatic patients because it is non-invasive. This research proposal proposes a novel approach for diagnosis of NASH and will be the first study to measure individual components of NASH (fat, inflammation and fibrosis) with quantitative ultrasound (QUS) scores. This study is timely because NASH is the second leading cause of liver transplantation in North America and is predicted to become the leading indication in the near future.

Participants needed: 102
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre hospitalier de l'Université de Montréal (CHUM)Updated: Mar 18, 2025Locations: 1
Eligibility criteria

Are at least 18 years old at screening; [+5]

Are pregnant or trying to become pregnant; [+6]