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About
The study will evaluate whether betaine reduces liver injury in people with metabolic dysfunction-associated steatohepatitis (MASH). MASH is a type of liver disease that occurs in some people with fatty liver. Betaine is a normal component in the human body and will be taken as a pill.
Seventy (70) participants will be randomized to receive either betaine or placebo for 24 weeks. After stopping treatment, participants will be seen in clinic for another 24 weeks (total participation in the study is approximately 1 year). Procedures performed during the study include blood tests, MRI examinations, questionnaires, and clinic visits.
We will measure improvement in liver injury with blood tests and with MRI.
Full description
Study Description: This is a randomized, double-masked phase II trial to test the hypothesis that 24 weeks of treatment with oral betaine, 2 g/day, is a safe and effective treatment for participants with serologically diagnosed metabolic dysfunction-associated steatohepatitis (MASH) and elevated serum alanine aminotransferase (ALT) level.
A total of 70 participants will be randomized at VA Long Beach. Primary endpoint is resolution of at-risk MASH determined by NIS2+™ score at the end of treatment (Week 24). Total study duration for each participant is up to 56 weeks (including screening, treatment, and follow-up).
Primary Objective: To evaluate the efficacy of betaine 2 g/day in reducing liver injury as assessed by percent of participants with NIS2+™ <0.6815 (ie, no longer having at-risk MASH) at the end of treatment (Week 24).
Secondary Objectives:
To evaluate the efficacy of betaine 2 g/day in reducing liver steatosis as assessed by percent of participants with >30% decrease in MRI proton density fat fraction (PDFF) at Week 24 (end of treatment).
To evaluate the safety and tolerability of betaine 2 g/d
Primary Endpoint: The primary endpoint is percent of participants with NIS2+™ <0.6815 (no longer having at-risk MASH) at Week 24 (end of treatment).
Secondary Endpoints:
The percentage of participants with >30% decline in MRI-PDFF at Week 24 (end of treatment).
Safety and tolerability based on adverse events, clinical laboratory values, vital signs, and patient report.
Exploratory Endpoints: There are 5 independent groups of exploratory endpoints: efficacy, cardiovascular risk, laboratory safety, betaine metabolites, and change in behavior and weight.
Study Population: 70 adults of either sex with serologically-diagnosed metabolic dysfunction-associated steatohepatitis and an ALT ≥50 U/L.
Phase: 2 Facilities Enrolling Participants: VA Long Beach Healthcare System Study Intervention: Group 1: betaine (oral, 1 gram BID) + standard of care Group 2: placebo (oral, BID) + standard of care
Study Duration: 5 years
Participant Duration: Participant participation is approximately 13 months:
Treatment: 24 weeks Post-treatment follow-up: 24 weeks
Statistical Assumptions Treatment groups 2 Randomization 1:1 Sample size estimates A two-sided two-sample Z-test with continuity correction and pooled variance Sample size 70 (35 per group) (includes drop outs) Analysis dataset All randomized participants who received at least one does of study medicine
Enrollment
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Inclusion and exclusion criteria
Patients must satisfy all the following criteria to be eligible for enrollment.
An individual who meets any of the following criteria will be excluded from participating in this trial.
Use of FDA-approved medications for the treatment of MASH within the prior 6 months or anticipated to use an FDA-approved medications for MASH during the next 12 months.
Use of a glucagon-like peptide-1 receptor agonist (GLP-1 RA) or GLP-1/GIP receptor agonist in the prior 6 months or anticipated use during the next 12 months.
Use of a medicine designed to reduce weight within the prior 6 months or anticipated use in the next 12 months.
Received insulin within the past 90 days or anticipation of needing insulin in the next 6 months.
Uncontrolled diabetes defined as HbA1c of 9.5% or higher within 60 days prior to enrollment.
Unstable body weight defined as >5% self-reported (or documented) change in body weight in the period in the 90 days prior to screening.
Moderate or heavy alcohol more than 1 week/month during the 3 months prior to screening. Moderate alcohol use is defined as more than 20 g/day (>14 drinks/week) in females or more than 30 g/day (>21 drinks per week) in males. A drink is defined as 12 ounces of beer, 5 ounces of wine, or 1.5 ounces of 80-proof spirits, or the equivalent amount of alcohol in other alcoholic drinks.
Phosphatidylethanol (PEth) test > 50 ug/L. (NOTE: PEth will be performed at screening. Participants with PEth >50 ug/L will be excluded. Repeat testing of PEth in participants with a PEth >50 ug/L at screening is not permitted.)
Inability to reliably quantify alcohol consumption based upon local study physician judgement.
Use of corticosteroids at a does equal to or greater than 10 mg/day of prednisone, for more than 5 days within the prior 30 days.
Continued use of drugs historically associated with NAFLD (amiodarone, methotrexate, systemic glucocorticoids, tetracyclines, tamoxifen, estrogens at doses greater than those used for hormone replacement, anabolic steroids, valproic acid, and other known hepatotoxins) for more than 2 weeks in the 6 months prior to randomization.
Cirrhosis of the liver, defined as any of the following:
The following laboratory tests during screening (or on blood tests performed within 60 days prior to randomization, if they are not repeated during screening):
Evidence of other forms of chronic liver disease:
Primary sclerosing cholangitis
Known history of Wilson disease, alpha-1-antitrypsin liver disease, or hemochromatosis. Any other type of liver disease that is currently active other than MASH such as drug-induced liver disease, liver cancer, or bile duct obstruction.
History of biliary diversion or evidence of current biliary obstruction.
Hospitalization for more than 3 days during the prior 60 days.
Known positivity for Human Immunodeficiency Virus (HIV) infection.
Any of the following in the past: myocardial infarction, stroke, or classification of heart failure New York Heart Association (NYHA) Class II, III, or IV
Hospitalization for unstable angina pectoris or transient ischemic attack within 6 months prior to randomization.
Current suspected cancer or a prior history of cancer, other than basal cell carcinoma of the skin that was surgically removed.
Active, serious medical disease with likely life expectancy less than 5 years
Active substance abuse including inhaled or injection drugs in the year prior to screening.
Female who is pregnant, breast-feeding, or intends to become pregnant, or is of
childbearing potential and not using a highly effective contraceptive method.
Current use of choline, betaine, or S-adenosylmethionine supplements, or refusal to abstain from their use during the study.
Participation in an IND trial in the 60 days before randomization
Any other condition which, in the opinion of the investigator, would impede compliance or hinder completion of the study, including inability to swallow treatment capsules.
Failure or inability to give informed consent.
Primary purpose
Allocation
Interventional model
Masking
70 participants in 2 patient groups, including a placebo group
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Central trial contact
Aliya A Uddin, MPH; Timothy R Morgan, MD
Data sourced from clinicaltrials.gov
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