Low-dose pioglitazone for treating liver disease in diabetes patients

Effect of Low-Dose Pioglitazone in Patients With Nonalcoholic Steatohepatitis (NASH)

This study is testing if a low dose of pioglitazone can improve liver health in people with type 2 diabetes and a specific liver condition called NASH.

Quick facts

• Phase: Phase 2
• Study type: Interventional
• Enrollment: 166 (estimated)
• Ages: 21 Years to 75 Years
• Sex: All
• Sponsor: University of Florida (Academic / other)
• Drugs / interventions: methotrexate, prednisone
• Locations: 1 site (Gainesville, Florida)
• Trial ID: NCT04501406 on ClinicalTrials.gov

What this trial studies

This clinical trial aims to evaluate the safety and efficacy of low-dose pioglitazone (15 mg per day) in patients aged 21 to 75 with type 2 diabetes and biopsy-proven nonalcoholic steatohepatitis (NASH). The study is designed as a 72-week randomized, double-blind, placebo-controlled trial, where participants will be assigned to receive either pioglitazone or a placebo. The primary focus is to assess changes in liver histology and metabolic parameters. Previous studies have shown that higher doses of pioglitazone are effective, but this trial will explore the effects of a lower dose on liver health.

Who should consider this trial

Good fit: Ideal candidates are adults aged 21 to 75 with type 2 diabetes and confirmed NASH through liver biopsy.

Not a fit: Patients with liver disease not related to NASH or those with uncontrolled diabetes may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a safer and effective option for managing liver disease in patients with type 2 diabetes.

How similar studies have performed: Previous studies have shown that higher doses of pioglitazone are effective in similar patient populations, but the low-dose approach is novel.

Eligibility criteria

Inclusion criteria:

1. Able to communicate meaningfully with the investigator and legally competent to provide written informed consent.
2. Aged 21 to 75 years.
3. Patients with a diagnosis T2DM based on prior medical history, medication use, or results from a fasting plasma glucose or hemoglobin A1c, according to American Diabetes Association guidelines.
4. Patients will be allowed to participate the glycosylated hemoglobin (HbA1c) is ≤ 9.5% on diet alone or on a stable dose (for at least 2 months) of the following diabetes medications: metformin, sulfonylurea, acarbose, DPP-IV inhibitors, SGLT2 inhibitors or insulin. The insulin total daily dose should be stable (defined as within 20% for the prior 2 months prior to study entry). A GLP-1 receptor agonist will be allowed if on a stable dose for 6 months prior to enrollment and body weight stable (defined as within 3%) in the prior 3 months. Diabetes medications will be continued at stable doses during the entire study (except if glycemic control deteriorates based on HbA1c; addition of metformin, sulfonylurea, acarbose, DPP-IV or insulin will be allowed if needed; pioglitazone, GLP-1RA or SGLT2 inhibitors will not).
5. Hemoglobin level of at least 11.0 g/L (men) or at least 10.0 g/L (women), leukocyte count of at least 3.0 × 109 cells/L, neutrophil count of at least 1.5 × 109 cells/L, platelet count of at least 100 × 109 cells/L, albumin level of at least 2.5 g/L, serum creatinine level of 2.5 mg/dL or less, INR \> 1.4, bilirubin \> 1.3 mg/dL (unless if non-conjugated bilirubin elevated in the setting of Gilbert's syndrome), and AST and ALT levels no more than 8 times the ULN.

Exclusion criteria:

1. Past or current history of alcohol use (\>20 g/d of ethanol in females or \>30g/d in males). Alcohol abuse will be ruled out on the basis of physicians' judgment, self-reported alcohol use, and family members' report of the patient's alcohol use. In addition, the Alcohol Use Disorders Identification Test (AUDIT) score will be used to assess alcohol use.
2. Receipt of long-term therapy with medications known to have adverse effects on glucose tolerance, unless the patient has been receiving a stable dose of such agents for 4 weeks before study entry.
3. Use of medications that could induce steatosis, such as estrogen or other hormonal replacement therapy, amiodarone, methotrexate, tamoxifen, raloxifene, pharmacological doses of oral glucocorticoids (≥10 mg per day of prednisone or equivalent), or chloroquine.
4. Use of vitamin E (doses ≥800 IU/dy) or pioglitazone or any FDA-approved drug for NASH to be approved during the study.
5. Any cause of chronic liver disease other than NASH, including but not restricted to alcohol or drug abuse, medication, chronic hepatitis B or C virus infection, autoimmune liver disease, hemochromatosis, Wilson disease (if younger than age 50), α1-antitrypsin deficiency, history of exposure to hepatotoxic drugs or history of primary or metastatic liver cancer.
6. Presence of other medical conditions known to cause fatty liver disease.
7. Any clinical or laboratory evidence of cirrhosis or hepatic decompensation, such as history of ascites, esophageal bleeding varices, or spontaneous encephalopathy.
8. Prior or scheduled surgical procedures, including gastroplasty or jejunoileal or jejunocolic bypass.
9. Prior exposure to organic solvents, such as carbon tetrachloride.
10. Total parenteral nutrition within the past 6 months.
11. Patients with other forms of diabetes other than T2DM.
12. History of clinically significant heart disease such as congestive heart failure (New York Heart Association Classification greater than grade II-IV), unstable cardiovascular disease such as unstable angina (i.e., new or worsening symptoms of coronary heart disease within the past 6 months), acute coronary syndrome or coronary artery intervention within the past 6 months, acute myocardial infarction in the past 6 months; history of (within prior 6 months) or current unstable cardiac dysrhythmias.
13. Uncontrolled hypertension (systolic blood pressure \>160 mmHg and/or diastolic blood pressure \>100 mmHg); clinically evident peripheral vascular disease (history of claudication); stroke or transient ischemic attack within the prior 6 months; clinically significant pulmonary disease (dyspnea on exertion of ≤1 flight; abnormal breath sounds on auscultation), or kidney disease as defined above per plasma creatinine elevation or significant proteinuria (macroalbuminuria).
14. Pregnancy or lactation in women. Must have a negative pregnancy test or at least be two-year post-menopausal. Women with childbearing potential (i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile) must be using a highly effective method of contraception (i.e. combined (estrogen and progesterone containing) hormonal/ progesterone-only hormonal contraception associated with inhibition of ovulation, intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomized partner). The contraceptive method will have to be followed for at least one menstruation cycle after the end of the study.
15. History of malignancy in the past 5 years and/or active neoplasm with the exception of resolved superficial nonmelanoma skin cancer.
16. History of bladder disease and/or hematuria or has current hematuria unless due to a recent urinary tract infection.
17. Hemostasis disorders or current treatment with anticoagulants.
18. Any other criteria that based on the assessment of the research team the patient is deemed to be a poor research candidate.

Where this trial is running

Gainesville, Florida

• University of Florida — Gainesville, Florida, United States (Recruiting)

Study contacts

• Principal investigator: Kenneth Cusi, MD — University of Florida
• Study coordinator: Kenneth Cusi, M.D.

Conditions Type 2 Diabetes Mellitus; Nonalcoholic Steatohepatitis; Nonalcoholic fatty liver disease; pioglitazone.