Study of Gemcabene in Adults With FPLD
An Investigator-Initiated Open-Label, Randomized Study of Gemcabene in Adults With Familial Partial Lipodystrophy Disease (FPLD)
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Locations
-
-
Michigan
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Ann Arbor, Michigan, United States, 48105
- University of Michigan
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-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
- Clinical diagnosis of lipodystrophy based on a lack of body fat in a partial fashion assessed by physical examination, and at least 1 MAJOR criterion (below):
- Low skinfold thickness in anterior thigh by caliper measurement: men (≤ 10 mm) and women (≤ 22 mm) OR
- Historic genetic diagnosis of familial partial lipodystrophy (e.g. mutations in LMNA, PPAR-γ, AKT2, or PLIN1 genes) as supported by source documentation
- Hepatic steatosis (>10% - Stage 2 or 3) as demonstrated by MRI-PDFF;
- Alcohol intake of less than 20 g per day in females and 30 g per day in males (one 12 oz beer, one glass of wine, or 2 oz of spirits or liquor equals roughly 10 g of alcohol;
- Mean fasting triglyceride value ≥ 250 mg/dL at the Screening Visit;
- Background lipid lowering medications must be stable for at least 6 weeks prior to the Screening Visit;
- Women patients must not be pregnant or lactating and women of child-bearing potential must agree to use acceptable methods of contraception throughout the duration of the study and for 30 days after the last dose of study drug. Male patients must agree to use contraception by means of a condom and may not donate sperm throughout the duration of the study and for 8 days after the last dose of study drug.
- Weight greater than 50 kg (~110 lbs); with a body mass index (BMI) of no more than 45 kg/m²;
- Have not used a fibrate with in the last 6 weeks and/or thiazolidinediones (TZDs) within the last 12 weeks prior to the Screening visit.
- Do not have a hypersensitivity or a history of significant reactions of fibrates.
- Are not currently taking potent CYP3A4 inhibitors such as itraconazole or a macrolide antibiotic.
- Have a condition or finding which, in the opinion of the Investigator, would compromise the patient's safety or participation in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Group 1: 300 mg Gemcabene daily week 12-24
Patients took Gemcabene 300mg daily for weeks 1-12.
After 12 weeks, at visit T4, patients were randomized 1:1 according to pre-generated randomization code.
This arm received 300mg Gemcabene daily for 12 weeks total, starting at week 12.
|
300mg Gemcabene
|
|
Experimental: Group 2: 600mg Gemcabene daily week 12-24
Patients took Gemcabene 300mg daily for weeks 1-12.
After 12 weeks, at visit T4, patients were randomized 1:1 according to pre-generated randomization code.
This arm received 600mg Gemcabene daily for 12 weeks total, starting at week 12.
|
600mg Gemcabene
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Fasting Serum Triglyceride (at 12 Weeks)
Time Frame: Baseline to week 12
|
This is measured by percent change in fasting serum triglyceride from baseline to week 12
|
Baseline to week 12
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Fasting Serum Triglycerides (Through 24 Weeks)
Time Frame: Baseline, week 6 and week 12, week 24
|
This is measured by change in fasting serum triglyceride from baseline to average of weeks 6 and 12, and week 24 and change in fasting serum triglyceride from baseline to week 12
|
Baseline, week 6 and week 12, week 24
|
|
Percent Change in Fasting Serum Triglycerides (Through 24 Weeks)
Time Frame: Baseline, week 6 and week 12, week 24
|
This is measured by percent change in fasting serum triglyceride from baseline to average of weeks 6 and 12, and week 24 and change in fasting serum triglyceride from baseline to week 12
|
Baseline, week 6 and week 12, week 24
|
|
Change in Liver Fat Content as Measured by Magnetic Resonance Imaging - Protein Density Fat Fraction (MRI-PDFF)
Time Frame: Baseline, week 12, week 24
|
This is measured by change in liver fat content using Magnetic Resonance Imaging - Protein Density Fat Fraction (MRI-PDFF) from baseline to week 12 and week 24
|
Baseline, week 12, week 24
|
|
Percent Change in Liver Fat Content as Measured by Magnetic Resonance Imaging - Protein Density Fat Fraction (MRI-PDFF)
Time Frame: Baseline, week 12, week 24
|
This is measured by percent change in liver fat content using Magnetic Resonance Imaging - Protein Density Fat Fraction (MRI-PDFF) from baseline to week 12 and week 24
|
Baseline, week 12, week 24
|
|
Change in Liver Fibrosis
Time Frame: Baseline, Week 12, and Week 24
|
This is measured by change in liver fibrosis using MR-elastography from baseline to week 12 and week 24
|
Baseline, Week 12, and Week 24
|
|
Percent Change in Liver Fibrosis
Time Frame: Baseline, Week 12, and Week 24
|
This is measured by percent change in liver fibrosis using MR-elastography from baseline to week 12 and week 24
|
Baseline, Week 12, and Week 24
|
|
Change in NAS (Non-alcoholic Steatohepatitis)
Time Frame: Baseline to week 24
|
This is measured by change in NAS via non-alcoholic fatty liver disease activity score.
NAS is the unweighted sum of steatosis, lobular inflammation and hepatocyte ballooning from baseline to week 24.
Total NAS scores can range from 0 to 8. The higher the NAS score, the more severe the liver disease.
|
Baseline to week 24
|
|
Percent Change in NAS (Non-alcoholic Steatohepatitis)
Time Frame: Baseline to week 24
|
This is measured by change in NAS via non-alcoholic fatty liver disease activity score.
NAS is the unweighted sum of steatosis, lobular inflammation and hepatocyte ballooning from baseline to week 24.
Total NAS scores can range from 0 to 8. The higher the NAS score, the more severe the liver disease.
|
Baseline to week 24
|
|
Change in Cholesterol
Time Frame: Baseline, week 6 and week 12, week 24
|
This will be measured by change in total, HDL and LDL levels in mg/dL
|
Baseline, week 6 and week 12, week 24
|
|
Percent Change in Cholesterol
Time Frame: Baseline, week 6 and week 12, week 24
|
This will be measured as percent change in total, HDL and LDL levels in mg/dL.
|
Baseline, week 6 and week 12, week 24
|
|
Change in Apolipoprotein
Time Frame: Baseline, week 6 and week 12, week 24
|
This will be measured by change in apolipoprotein A and B in mg/dL
|
Baseline, week 6 and week 12, week 24
|
|
Percent Change in Apolipoprotein
Time Frame: Baseline, week 6 and week 12, week 24
|
This will be measured by percent change in apolipoprotein A and B in mg/dL
|
Baseline, week 6 and week 12, week 24
|
|
Change in High-Sensitivity C-Reactive Protein (hsCRP)
Time Frame: Baseline, week 12, week 24
|
This is measured by change in high-sensitivity C-reactive protein (hsCRP) from baseline to weeks 12 and week 24
|
Baseline, week 12, week 24
|
|
Percent Change in High-Sensitivity C-Reactive Protein (hsCRP)
Time Frame: Baseline, week 12, week 24
|
This is measured by percent change in high-sensitivity C-reactive protein (hsCRP) from baseline to weeks 12 and week 24
|
Baseline, week 12, week 24
|
|
Change in Alanine Aminotransferase (ALT)
Time Frame: Baseline, week 12, week 24
|
This is measured by change in alanine aminotransferase (ALT) from baseline to weeks 12 and week 24
|
Baseline, week 12, week 24
|
|
Percent Change in Alanine Aminotransferase (ALT)
Time Frame: Baseline, week 12, week 24
|
This is measured by percent change in alanine aminotransferase (ALT) from baseline to weeks 12 and week 24
|
Baseline, week 12, week 24
|
|
Change in Aspartate Aminotransferase (AST)
Time Frame: Baseline, week 12, week 24
|
This is measured by change in aspartate aminotransferase (AST) from baseline to weeks 12 and week 24
|
Baseline, week 12, week 24
|
|
Percent Change in Aspartate Aminotransferase (AST)
Time Frame: Baseline, week 12, week 24
|
This is measured by percent change in aspartate aminotransferase (AST) from baseline to weeks 12 and week 24
|
Baseline, week 12, week 24
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Elif A Oral, M.D., University of Michigan
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Metabolic Diseases
- Skin Diseases
- Liver Diseases
- Genetic Diseases, Inborn
- Lipid Metabolism Disorders
- Hyperlipidemias
- Dyslipidemias
- Laminopathies
- Skin Diseases, Metabolic
- Fatty Liver
- Non-alcoholic Fatty Liver Disease
- Hypertriglyceridemia
- Lipodystrophy
- Lipodystrophy, Familial Partial
Other Study ID Numbers
Other Study ID Numbers
- HUM00130803
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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