A Study to Compare MitoQ and Placebo to Treat Non-alcoholic Fatty Liver Disease (NAFLD) (MARVEL)

A Double-blind Randomised Placebo-controlled Multicentre Study of 40mg MitoQ and Placebo for the Treatment of Participants With Raised Liver Enzymes Due to Non-Alcoholic Fatty Liver Disease (NAFLD)

The purpose of this study is to investigate whether a new medicine, called mitoquinone, will reduce raised liver enzymes due to NAFLD and to see if it is safe.

Study Overview

• Status: Terminated
• Conditions: Non-alcoholic Fatty Liver Disease
• Intervention / Treatment: Drug: Placebo; Drug: Mitoquinone mesylate

• Study Type: Interventional
• Enrollment (Anticipated): 110
• Phase: Phase 2

Contacts and Locations

Study Locations

• United Kingdom
  • Newcastle-upon-Tyne, United Kingdom, NE2 4HH
    • Freeman Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 70 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Provide written informed consent
2. NAFLD as determined by raised ALT (> 1.5 x ULN corresponding to >29U/L for females and >45U/L for males] in the screening period and on at least two other occasions in the previous 6 months) and ultrasound evidence of steatosis (in the previous 12 months).
3. Be aged between 18 - 70 years on the day of consent
4. Expect to not require or make any changes in all their current concomitant medications (prescribed and over-the-counter) for the duration of their participation in the study
5. Female patients with reproductive potential must have a negative serum pregnancy test within 14 days prior to start of trial and must agree to use a medically acceptable method of contraception throughout the treatment period and for 1 month after discontinuation of treatment. Acceptable methods of contraception include IUD, oral contraceptive, subdermal implant and double barrier (condom with a contraceptive sponge or contraceptive pessary)

Exclusion Criteria:

1. Alcohol consumption > 14 units/week for females and 21 units/week for males
2. Hepatocellular carcinoma (HCC) or suspicion of HCC
3. Presence of human immunodeficiency virus (HIV), Hepatitis B (HBV) or Hepatitis C (HCV)
4. Renal impairment (creatinine > 1.5 x ULN) or hepatorenal syndrome
5. Chronic pancreatitis
6. Hospitalization for liver disease within 60 days of the baseline visit
7. Previously diagnosed diabetes / treatment with insulin sensitizing agents
8. Severe or morbid obesity (BMI>40kg/m2)
9. ALT or AST > 10 times ULN
10. Liver transplant recipients
11. Corticosteroids in the past 30 days
12. Any participant who has received any investigational drug or device within 30 days of dosing, or who is scheduled to receive another investigational drug or device during the course of this trial
13. A history of a malignancy other than treated basal cell or squamous cell carcinoma of the skin; those with a history of malignancy that has been treated with no recurrence within the last 2 years are not excluded
14. Females who are pregnant or breastfeeding
15. Use of Coenzyme Q10, either prescribed or purchased over-the-counter, are prohibited during the study, except for doses of up to 25mg/day which have been stable for 30 days prior to baseline. Higher doses require a 7 day washout prior to baseline.
16. Use of Vitamin E, either prescribed or purchased over-the-counter, are prohibited during the study, except for doses of up to 200IU/day which have been stable for 30 days prior to baseline. Higher doses require a 90 day washout prior to baseline.
17. Any changes to prescription medication in the 30 days prior to baseline
18. A history of a hypersensitivity reaction to any components of the study drug or structurally similar compounds including Coenzyme Q10 and idebenone
19. Unable to swallow tablets whole
20. Patients with histological or clinical evidence of established cirrhosis
21. Suffering from any other disease or condition which, in the opinion of the investigator, means that it would not be in the patient's best interest to participate in this study

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Mitoquinone mesylate tablets (MitoQ)	Drug: Mitoquinone mesylate; 2 tablets to be taken daily upon wakening, with a glass of water and at least one hour before food.
Placebo Comparator: Matching placebo tablet	Drug: Placebo; Placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Percentage change in ALT (relative to baseline) at the end of the treatment period (Day 90) for MitoQ compared with placebo.	Baseline and 3 months

Secondary Outcome Measures

Outcome Measure	Time Frame
Absolute change in ALT level (relative to baseline) at end of treatment period for MitoQ compared with placebo	Baseline and 3 months
The percentage of participants whose ALT levels are in the normal range at the end of the treatment period.	3 months
The difference in the percentage and absolute rates of change in ALT levels between MitoQ and placebo.	Baseline to 3 months
The percentage and absolute change in AST at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
The change in HOMA-IR at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
The change in HbA1c at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
The percentage and absolute change in GGT and alkaline phosphatase at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
Areas under the ALT, AST, GGT and alkaline phosphatase curves from baseline to the end of the treatment period.	Baseline to 3 months
The change in markers of liver inflammation (leptin and adiponectin) at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
The change in biomarkers of mitochondrial function and oxidative damage (isoprostanes) at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
The change in blood pressure at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
The change in blood lipid profile at the end of the treatment period (relative to baseline) for MitoQ compared with placebo.	Baseline and 3 months
Incidence of adverse events	Baseline to Follow-up (total 4 months)
Clinically relevant deterioration in laboratory variables	Baseline to Follow-up (total 4 months)
Clinically relevant deterioration in vital signs	Baseline to Follow-up (total 4 months)
Clinically relevant deterioration in ECG parameters	Baseline to Follow-up (total 4 months)

Collaborators and Investigators

• Sponsor: Antipodean Pharmaceuticals, Inc.
• Investigators: Principal Investigator: Chris Day, MD, PhD, Newcastle University Medical School, UK

Study record dates

Study Major Dates

• Study Start: November 1, 2010
• Primary Completion (Anticipated): June 1, 2011
• Study Completion (Anticipated): July 1, 2011

Study Registration Dates

• First Submitted: July 19, 2010
• First Submitted That Met QC Criteria: July 20, 2010
• First Posted (Estimate): July 22, 2010

Study Record Updates

• Last Update Posted (Estimate): June 1, 2011
• Last Update Submitted That Met QC Criteria: May 28, 2011
• Last Verified: May 1, 2011

More Information

Terms related to this study

• Keywords: Non-alcoholic fatty liver disease; Placebo-controlled; Double-blind; NAFLD
• Additional Relevant MeSH Terms: Digestive System Diseases; Liver Diseases; Fatty Liver; Non-alcoholic Fatty Liver Disease
• Other Study ID Numbers: MTQ-LD-001; 2010-021368-13 (EudraCT Number)