Study to Evaluate the Effect of Elafibranor on Hepatic Lipid Composition in Subjects With Nonalcoholic Fatty Liver (NAFL)
Phase 2
Terminated
- Conditions
- Non-Alcoholic Fatty Liver
- Interventions
- Drug: Placebo
- Registration Number
- NCT03953456
- Lead Sponsor
- Genfit
- Brief Summary
This randomized, double-blind, cross-over (placebo or elafibranor \[GFT505\]) placebo-controlled study, will evaluate the effect on hepatic lipid composition and safety of elafibranor 120 mg quaque die (QD) versus placebo in an adult NAFL population after 6 weeks of treatment with a 4-week wash-out period. This study will achieve mechanistic information about the mode of action of Elafibranor on the (lipid) metabolism in the human fatty liver
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 17
Inclusion Criteria
- Males or post-menopausal females aged from 40-75 years inclusive at first Screening Visit. (Post-menopausal defined as: subject should be surgically sterilized at least 6 months or no spontaneous menses for at least 1 year prior to screening)
- Must provide signed written informed consent and agrees to comply with the study protocol.
- Liver fat percentage ≥ 5 percent (as measured with Magnetic Resonance Spectroscopy)
- 25.0 ≤ BMI ≤ 38.0 kg/m^2
- Stable dietary habits and physical activity pattern (over 3 months prior to Screening Visit)
- Subject agrees not to change dietary habits and physical activity pattern, to follow diet and lifestyle recommendations and not to consume or use illicit drugs during the study up to end of treatment.
Exclusion Criteria
Medical history:
- Documented weight loss of more than 5 percent during the 6-month period prior to Screening Visit
- Contra-indications for magnetic resonance imaging / spectroscopy
- Known history of Type 1 and 2 diabetes
- Known chronic heart failure (Grade I to IV of New York Heart Association classification)
- History of clinically significant acute cardiac event within 6 months prior to Screening Visit such as: stroke, transient ischemic attack, or coronary heart disease (angina pectoris, myocardial infarction, revascularization procedures)
- Uncontrolled hypertension despite optimal antihypertensive therapy
- Other well documented causes of chronic liver disease according to standard diagnostic procedures.
- Symptoms of clinical depression
- Other concurrent medical (e.g., immunological, neoplastic, endocrine, hematological, gastrointestinal or neurological) or psychiatric condition, which, in the opinion of the Investigator, would place the subject at increased risk, preclude obtaining voluntary consent/assent or compliance with required study procedures, or would confound the objectives of study
- Known hypersensitivity to the investigation product or any of its formulation excipients
Concomitant medications and lifestyle:
- Fibrates are not permitted from 8 weeks before Screening up to end of treatment. Subjects taking statins or ezetimibe prior to Screening Visit 1 may participate if the dose has been stable for 3 months prior to Screening Visit 1 and no dose adjustments are anticipated
- Currently taking drugs that can induce steatosis/steatohepatitis including, but not restricted to: corticosteroids (parenteral & oral chronic administration only), amiodarone (Cordarone), tamoxifen (Nolvadex), and methotrexate (Rheumatrex, Trexall), which are not permitted 30 days prior to Screening and up to end of treatment
- Subjects receiving thiazolidinediones (glitazones [pioglitazone, rosiglitazone])
- Currently taking any medication that could interfere with study medication absorption, distribution, metabolism, or excretion or could lead to induction or inhibition of microsomal enzymes, e.g., indomethacin, which are not permitted from Randomization until end of treatment
- Any medication use known to interfere with glucose homeostasis/metabolism
- Smoking
- Current or recent history (<5years) of significant alcohol consumption. For men, significant consumption is typically defined as higher than 30 g pure alcohol per day. For women, it is typically defined as higher than 20 g pure alcohol per day
- Subjects who have donated blood or blood products within the previous month prior to screening or who plan to donate blood or blood products at any time during the trial and in the month following the end of the study
- Is participating in any other study and have received any other investigational drug or device within 30 days prior to Screening or are taking part in a non-medication study which, in the opinion of the Investigator, would interfere with study compliance or outcome assessments
- Subjects who cannot be contacted in case of emergency
In addition to the above criteria, subject should not present any of the following biological exclusion criteria:
- Positive anti-human immunodeficiency virus (HIV) antibody
- Positive hepatitis B surface antigen
- Positive hepatitis C Virus (HCV) antibody
- Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) >5 x upper limit of normal (ULN)
- Conjugated bilirubin > 1.50mg/dL due to altered hepatic function Note: Gilbert Disease subjects are allowed into the study
- International normalized ratio >1.40 due to altered hepatic function
- Platelet count <100,000/mm^3 due to portal hypertension
- Serum creatinine levels >1.53 mg/dL in males and >1.24 mg/dL in females
- Significant renal disease, including nephritic syndrome, chronic kidney disease (defined as subjects with markers of kidney damage or estimated glomerular filtration rate (eGFR) of less than 60 ml/min/1.73 m^2)
- Unexplained serum creatine phosphokinase (CPK) >2 x ULN. In case of explained elevated CPK >2 x ULN, the measurement can be repeated prior to Randomization. In this case, retest should be performed within 1 to 2 weeks after initial test. A CPK retest >2 x ULN leads to exclusion
- Hemoglobin A1c (HbA1C) > 6.4% and/or fasting plasma glucose (FGP) > 126 mg/dl
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description elafibranor 120mg followed by placebo elafibranor 120mg Participants will first receive elafibranor 120mg for 6 weeks. After a washout period of 4-6 weeks, they will then receive placebo for 6 weeks elafibranor 120mg followed by placebo Placebo Participants will first receive elafibranor 120mg for 6 weeks. After a washout period of 4-6 weeks, they will then receive placebo for 6 weeks placebo followed by elafibranor 120mg elafibranor 120mg Participants will first receive placebo for 6 weeks. After a washout period of 4-6 weeks, they will then receive elafibranor 120mg for 6 weeks placebo followed by elafibranor 120mg Placebo Participants will first receive placebo for 6 weeks. After a washout period of 4-6 weeks, they will then receive elafibranor 120mg for 6 weeks
- Primary Outcome Measures
Name Time Method Change in relative amount of saturated fatty acids in the liver After 6 weeks Relative amount of saturated fatty acids (SFA) in the liver measured by Magnetic Resonance Spectroscopy (1H-MRS) at the end of 6 weeks treatment period
- Secondary Outcome Measures
Name Time Method Incidence of clinically meaningful changes from baseline in safety laboratory parameters, and vital signs After 6 weeks Incidence and severity of treatment emergent adverse events (TEAEs) and their relationship to study drug After 6 weeks Change in hepatic insulin sensitivity After 6 weeks Hepatic insulin sensitivity measured by Hepatic Glucose Production (HGP) at the end of 6 weeks treatment period
Glucose homeostasis markers After 6 weeks Fructosamine
Lipid metabolism markers After 6 weeks Free fatty acid (FFA)
Inflammatory markers After 6 weeks Haptoglobin
Liver function After 6 weeks Total and conjugated bilirubin
Renal function After 6 weeks Total proteins
Body weight After 6 weeks Body Mass Index After 6 weeks Waist circumference After 6 weeks
Trial Locations
- Locations (1)
NUTRIM School of Nutrition and Translational Research in Metabolism
🇳🇱Maastricht, Netherlands