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Clinical Trials/NCT06108219
NCT06108219
Active, not recruiting
Phase 2

A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Miricorilant in Adult Patients With Nonalcoholic Steatohepatitis/Metabolic Dysfunction-Associated Steatohepatitis (MONARCH)

Corcept Therapeutics154 sites in 2 countries175 target enrollmentOctober 25, 2023

Overview

Phase
Phase 2
Intervention
Placebo (Cohort B)
Conditions
Nonalcoholic Steatohepatitis (NASH)
Sponsor
Corcept Therapeutics
Enrollment
175
Locations
154
Primary Endpoint
Percent relative change from Baseline in liver-fat content assessed by MRI-PDFF (Cohort A and Cohort B)
Status
Active, not recruiting
Last Updated
11 days ago

Overview

Brief Summary

A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Miricorilant in Adult Patients with Nonalcoholic Steatohepatitis (MONARCH)

Detailed Description

Approximately 75 patients who are eligible for participation in the study will be randomized on Day 1 in a 2:1 ratio to 100 mg miricorilant or placebo twice weekly, for 48 weeks of treatment (Cohort A). Approximately 90 patients who are eligible for participation in the study will be randomized on Day 1 in a 2:1 ratio to 100 mg miricorilant twice a week for 6 weeks of treatment, followed by a dose escalation to 200 mg miricorilant or placebo twice weekly for an additional 18 weeks which resulting in a total treatment duration of 24 weeks, or to placebo for 24 weeks. (Cohort B).

Registry
clinicaltrials.gov
Start Date
October 25, 2023
End Date
September 1, 2026
Last Updated
11 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Cohort A: Histological diagnosis of NASH/MASH with NAS ≥ 4 (≥ 1 point in each subcomponent of steatosis, inflammation, and ballooning) and NASH-CRN fibrosis score of 2 or 3 based on the consensus method of histological assessment. A historical liver biopsy within 6 months of Screening with reading confirmed during the Screening period by a consensus panel is acceptable.
  • Cohort B: Have a liver biopsy result that does not meet with the criteria for inclusion in Cohort A and is consistent with one of the following based on the consensus method of histological assessment:
  • NAS ≥ 3 with ≥1 point in each subcomponent of steatosis, inflammation, and ballooning, and a NASH-CRN fibrosis score of F1 or
  • NAS ≥ 2 with ≥1 point in subcomponent of steatosis and ≥ 1 point in subcomponent of ballooning or inflammation and a NASH-CRN fibrosis score of F2 or 3
  • AST \> 17 U/L for women and AST \> 20 U/L for men.
  • FibroScan® liver stiffness measurement ≥ 8 kPa and CAP ≥ 280 dB/m.
  • MRI-PDFF with ≥ 8% steatosis
  • Presence of at least 1 of the following metabolic syndromes that increase the risk of NASH/MASH:
  • Diagnosis of type 2 diabetes OR
  • Presence of 2 or more components of metabolic syndrome:

Exclusion Criteria

  • Have participated in another clinical trial within the last 3 months of Screening where the patient received active treatment for NASH/MASH.
  • Have participated in a clinical trial for any other indication within the last 3 months or 5 half-lives of the treatment, whichever is longer.
  • Are pregnant or lactating women
  • Have a BMI \< 18 kg/m2 or \> 45 kg/m2.• Have had liver transplantation or plan to have liver transplantation during the study
  • Have type 1 diabetes or poorly controlled type 2 diabetes.
  • Are pregnant or lactating women
  • Have a BMI \< 18 kg/m2 or \> 45 kg/m2
  • Have had successful weight-loss surgery within 2 years prior to Screening or are planning weight-loss surgery during the study.
  • Have a \>5% weight change within 3 months prior to Screening.
  • Have significant alcohol consumption of more than 20 g per day for women and 30 g per day for men within 1 year prior to screening or score of ≥8 on AUDIT questionnaire

Arms & Interventions

Placebo (Cohort B)

Patients who meet the entry criteria for study CORT118335-862 (Cohort B) will be enrolled to receive a matching placebo twice a week for 24 weeks.

Intervention: Placebo (Cohort B)

Placebo (Cohort A)

Patients who meet the entry criteria for study CORT118335-862 (Cohort A) will be enrolled to receive a matching placebo twice a week for 48 weeks.

Intervention: Placebo (Cohort A)

Experimental (Cohort A)

Patients who meet the entry criteria for study CORT118335-862 (Cohort A) will be enrolled to receive 100 mg of miricorilant, twice a week for 48 weeks.

Intervention: Miricorilant (Cohort A)

Experimental (Cohort B)

Patients who meet the entry criteria for study CORT118335-862 (Cohort B) will be enrolled to receive 100 mg of miricorilant, twice a week for 6 weeks. Dose will be escalated to 200 mg of miricorilant, twice a week for 18 weeks.

Intervention: Miricorilant (Cohort B)

Outcomes

Primary Outcomes

Percent relative change from Baseline in liver-fat content assessed by MRI-PDFF (Cohort A and Cohort B)

Time Frame: Week 24

Secondary Outcomes

  • Change in lipids - total cholesterol, HDL, LDL, VLDL, TG, serum free fatty acids, apolipoproteins (Cohort A and Cohort B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Change in HbA1c (Cohort A and B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Change in liver stiffness and Controlled Attenuation Parameter (CAP) by FibroScan. (Cohort A and Cohort B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Change in absolute body weight (Cohort A and B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Change in Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) (Cohort A and Cohort B at Week 6 and 24, Cohort A at Week 48)(Week 6, 24 and 48)
  • Change in HOMA-IR (Cohort A and B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Change in plasma glucose (Cohort A and B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Change in ELF, Pro-C3 and other markers of liver fibrosis (Cohort A and B at Week 24, Cohort A at Week 48)(Week 24 and 48)
  • Absolute change from Baseline in liver-fat content by MRI-PDFF (Cohort A and B at Week 6 and 24, Cohort A at Week 48)(Week 6, 24, Week 48)
  • Percent relative change from Baseline in liver-fat content by MRI-PDFF (Cohort A and B at Week 6 and 24, Cohort A at Week 48)(Week 6 and 24, Week 48)
  • Resolution of steatohepatitis (defined as a ballooning grade of 0 and a lobular inflammation grade of ≤ 1) and no worsening of liver fibrosis at Week 48 assessed by biopsy (Cohort A).(Week 48)
  • Proportion of patients with at least 2 points reduction from Baseline in the NAS (NAFLD activity score) without worsening of liver fibrosis at Week 48 assessed by biopsy, with at least a 1-point reduction in ballooning or inflammation (Cohort A).(Week 48)
  • Improvement in liver fibrosis stage by at least 1-point (NASH CRN fibrosis score) from Baseline and no worsening of steatohepatitis at Week 48 assessed by biopsy (Cohort A).(Week 48)

Study Sites (154)

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