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A Phase 3 Study to Evaluate the Safety and Biomarkers of Resmetirom (MGL-3196) in Non Alcoholic Fatty Liver Disease (NAFLD) Patients (MAESTRO-NAFLD1)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04197479 |
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Recruitment Status :
Recruiting
First Posted : December 13, 2019
Last Update Posted : July 7, 2020
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Sponsor:
Madrigal Pharmaceuticals, Inc.
Information provided by (Responsible Party):
Madrigal Pharmaceuticals, Inc.
- Study Details
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Brief Summary:
A double-blind placebo controlled randomized Phase 3 study to evaluate the safety and tolerability of once-daily, oral administration of 80 or 100 mg resmetirom versus matching placebo. 100 patients will be enrolled in a 100 mg open-label arm.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Non-Alcoholic Fatty Liver Disease | Drug: Placebo Drug: Resmetirom | Phase 3 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 700 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | A 52-Week, Phase 3 Study to Evaluate Safety and Biomarkers of Resmetirom (MGL-3196) in Patients With Non-alcoholic Fatty Liver Disease (NAFLD) (MAESTRO-NAFLD-1) |
| Actual Study Start Date : | December 16, 2019 |
| Estimated Primary Completion Date : | December 2021 |
| Estimated Study Completion Date : | December 2021 |
Resource links provided by the National Library of Medicine
MedlinePlus Genetics related topics:
Non-alcoholic fatty liver disease
| Arm | Intervention/treatment |
|---|---|
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Experimental: Open label: resmetirom
100 mg daily
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Drug: Resmetirom
Tablet
Other Name: MGL-3196 |
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Placebo Comparator: Double blinded: matching placebo
Placebo daily
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Drug: Placebo
Matching tablets |
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Experimental: Double blinded: resmetirom 80 mg
80 mg daily
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Drug: Resmetirom
Tablet
Other Name: MGL-3196 |
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Experimental: Double blinded: resmetirom 100 mg
100 mg daily
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Drug: Resmetirom
Tablet
Other Name: MGL-3196 |
Primary Outcome Measures :
- The effect of once daily, oral administration of 80 or 100 mg resmetirom versus placebo on the incidence of adverse events. [ Time Frame: 52 weeks ]
Secondary Outcome Measures :
- The effect of once daily, oral administration of 80 or 100 mg resmetirom versus placebo on the percent change in low density lipoprotein C (LDL-C) from baseline to Week 24 [ Time Frame: 24 weeks ]
- The effect of once daily, oral administration of 80 or 100 mg resmetirom versus placebo on the percent change in apolipoprotein B (ApoB) from baseline to Week 24 [ Time Frame: 24 weeks ]
- The effect of once daily, oral administration of 80 or 100 mg resmetirom versus placebo on the percent change in hepatic fat fraction as determined by MRI-PDFF from baseline to Week 16. [ Time Frame: 16 weeks ]
- The effect of once daily, oral administration of 80 or 100 mg resmetirom versus placebo on the percent change in triglycerides (TGs) from baseline to Week 24 in patients with baseline TG > 150 mg/dL. [ Time Frame: 24 weeks ]
- The effect of once daily, oral administration of 80 or 100 mg resmetirom versus placebo after 52 weeks on N-terminal type III collagen propeptide (PRO-C3) in patients with baseline PRO-C3 ≥10 ng/mL. [ Time Frame: 52 weeks ]
Information from the National Library of Medicine
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Must be willing to participate in the study and provide written informed consent.
- Male and female adults ≥18 years of age.
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Suspected or confirmed diagnosis of NASH or NAFLD (presumed NASH):
- Fibroscan with kPa ≥5.5 and <8.5; CAP ≥280 dB.m-1 OR
- MRE >2 and <4.0; MRI-PDFF ≥8% liver fat consistent with steatosis and fibrosis stage ≥1 and <4. OR
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Recent liver biopsy (within past 2 years) documenting NASH/NAFLD with steatosis showing one of the following:
- NAS ≥4, steatosis ≥1, fibrosis stage 0 or 1A/1C with PRO-C3 <14
- NAS <4, steatosis ≥1, with fibrosis stage ≤3
- NAS ≥4, steatosis ≥1, fibrosis stage ≤3 without ballooning
- MRI-PDFF fat fraction ≥8% obtained during the Screening Period (baseline MRI-PDFF) or a historic MRI-PDFF ≤8 weeks old at the time of randomization.
- Stable dyslipidemia therapy for ≥30 days prior to randomization.
Exclusion Criteria:
- History of significant alcohol consumption for a period of more than 3 consecutive months within 1 year prior to Screening.
- Regular use of drugs historically associated with NAFLD.
- History of bariatric surgery or intestinal bypass surgery within the 5 years prior to randomization or planned during the conduct of the study.
- Weight gain or loss ≥5% total body weight within 12 weeks prior to randomization.
- HbA1c >9.0%.
- Glucagon-like peptide 1 [GLP-1] agonist therapy or high dose vitamin E (>400 IU/day) unless stable for 24 weeks prior to biopsy.
- Presence of cirrhosis on liver biopsy defined as stage 4 fibrosis.
- Diagnosis of hepatocellular carcinoma (HCC).
- Model for End-stage Liver Disease (MELD) score ≥12, as determined at Screening, unless due to therapeutic anti coagulation or Gilbert syndrome.
- Hepatic decompensation.
- Chronic liver diseases.
- Has an active autoimmune disease.
- Serum ALT >250 U/L.
- History of biliary diversion.
- Uncontrolled hypertension (either treated or untreated).
- Active, serious medical disease with a likely life expectancy <2 years.
- Participation in an investigational new drug trial in the 60 days or 5 half-lives, whichever is longer, prior to randomization.
- Any other condition which, in the opinion of the Investigator, would impede compliance, hinder completion of the study, compromise the well-being of the patient, or interfere with the study outcomes.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04197479
Contacts
| Contact: Edward Chiang | 267-520-0252 | info@madrigalpharma.com |
Locations
Show 67 study locations
Sponsors and Collaborators
Madrigal Pharmaceuticals, Inc.
Investigators
| Study Director: | Rebecca Taub, MD | Madrigal Pharmaceuticals, Inc. |
| Responsible Party: | Madrigal Pharmaceuticals, Inc. |
| ClinicalTrials.gov Identifier: | NCT04197479 |
| Other Study ID Numbers: |
MGL-3196-14 |
| First Posted: | December 13, 2019 Key Record Dates |
| Last Update Posted: | July 7, 2020 |
| Last Verified: | July 2020 |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
Keywords provided by Madrigal Pharmaceuticals, Inc.:
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NASH NASH resolution Fatty liver disease NAFLD Hyperlipidemia Resmetirom Thyroid hormone receptor beta |
Hepatic Fibrosis Thyroid hormone receptor agonist Cardiovascular Dyslipidemia Nonalcoholic steatohepatitis |
Additional relevant MeSH terms:
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Liver Diseases Fatty Liver Non-alcoholic Fatty Liver Disease Digestive System Diseases |