A Study to Assess ARI-3037MO on Hepatic Fat Metabolism in Patients With Dysglycemia and Evidence of Hepatic Steatosis

This randomized,double-blind, placebo-controlled study will enroll 36 men and women with a
diagnosis of NAFLD orNASH. The study will be conducted over a period of approximately 28 wks
and will include:a Screening Phase (Days -14to -1); a 24-week long Treatment Phase, during
which patients will be randomly assigned to receive ARI-3037MO or placebo; an End-of-study
Visit (ESV) scheduled 2 wks after the end of the Treatment Phase The Screening Phase will
include 2 visits. Visit 1:There will be an initial assessment of a patient's eligibility for
participation in the study. A complete medical history will be obtained and prospective
study patients will undergo physical examinations and laboratory evaluations. For patients
who have had a liver biopsy in the 6months prior to Visit 1, the histology findings, i.e.,
NAS, steatosis score and fibrosis score will be recorded. Visit 2:Approximately 1 week after
Visit 1, and after the results of clinical laboratory screening test results have been
reviewed by the Principal Investigator (PI), patients will be contacted to advise them of
their eligibility to continue in the study. Eligible patients will undergo liver magnetic
resonance imaging (MRI) to assess intrahepatic fat content. Treatment Phase Patients with
MRI results showing intrahepatic fat content of ≥10% will be entered into the Treatment
Phase of the study. The Treatment Phase will include 4 outpatient visits over a period of 24
weeks. Visit 3:Patients will be randomly assigned to receive ARI-3037MO or placebo on Day 1
of a 24-week long outpatient treatment period. Baseline assessments, including FibroTest®,
FibroScan® and clinical laboratory tests, will be performed, and patients will take study
drug twice daily. Visits 4, 5 and 6: During the Treatment Phase, patients will visit the
study clinic at 4, 12 and 24 weeks (± 4 days) after Day 1 for evaluations and examinations
and to collect study drug. Twenty-four weeks after the start of dosing, at the end of the
Treatment Phase, patients will undergo a follow-up MRI and FibroScan† to assess change from
baseline in intrahepatic fat content and liver fibrosis, respectively.

†If FibroScan equipment is available at the study site End-of-Study Visit Visit 7:An ESV
will occur 2 weeks (± 4 days) after the end of the Treatment Phase.

Inclusion Criteria:

1. Male and female patients ≥ 18 years of age at study entry

2. Female patients must be of nonchildbearing potential

3. Have a stable diet and agree to maintain this diet throughout the study

4. Have not gained or lost ≥ 10 lbs (4.5 kg) of body weight within 6months prior to
Screening Visit 1

5. Have a body mass index (BMI) between 28 and 45 kg.m-2, inclusive

6. Have elevated alanine aminotransferase (ALT) levels. For men: 50 IU/L to 250 IU/L,
inclusive. For women: 40 IU/L to 240 IU/L, inclusive.

7. Have HbA1c of < 9.5

8. Have a intrahepatic fat content of ≥ 10% confirmed by liver MRI

9. If taking antidiabetic therapies (excluding thiazolidines as per exclusion Criterion
No. 13), i.e., metformin, sulfonylureas, dipeptidyl peptidase-4 inhibitors, insulin;
must be on a stable dose for at least 3months prior to Screening Visit 1. Similarly,
if taking lipid lowering therapies; must be on a stable dose for at least 3 months
prior to Screening Visit 1.

10. Understands the study requirements and the treatment procedures, is willing to comply
with all protocol-required evaluations and provides written informed consent before
any study specific tests or procedures are performed

Exclusion Criteria:

1. A history of hepatic disease such as chronic hepatitis C virus or concurrent active
hepatitis B virus (i.e., serum positive for hepatitis B surface antigen)

2. Autoimmune hepatitis

3. Primary biliary cirrhosis

4. Sclerosing cholangitis

5. Hereditary hemochromatosis

6. History of chronic / repeat blood transfusion (i.e., ≥ 20 units of blood)

7. Alpha-1 anti-trypsin deficiency

8. Wilson's disease

9. Thyroid disease

10. Bariatric surgery within 5 years prior to Screening Visit 1

11. Hepatic disease due to substance abuse

12. Have any concurrent disease or condition not listed above that, in the opinion of the
PI, would make the patient unsuitable for participation in the study

13. Currently taking thiazolidines (glitazone therapy, i.e., Rosiglitazone, Pioglitazone)

14. Liver biopsy in the past 90 days with negative results for cirrhosis and steatosis

15. No evidence of hepatic decompensation or elevated serum bilirubin > 1.5 times the
upper limit of normal

16. Estimated glomerular filtration rate < 60 mL/min according to the Modification of
Diet in Renal Disease equation

17. Known substance abuse

18. Current smoker or a history of smoking (> 10 cigarettes, > 3 cigars or > 3 pipes/day)

19. Current consumption of > 3 units of alcohol per day (> 21 units per week) for men and
> 2 units of alcohol per day (> 14 units per week) for women

20. Currently participating in another clinical study