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Clinical Trials/NCT02421094
NCT02421094
Completed
Phase 2

Phase 2 Study to Evaluate Non-Invasive Imaging Methods in Efficacy Assessment of GR-MD-02 for the Treatment of Liver Fibrosis in Patients With NASH With Advanced Fibrosis

Galectin Therapeutics Inc.1 site in 1 country30 target enrollmentSeptember 2015

Overview

Phase
Phase 2
Intervention
GR-MD-02
Conditions
Nonalcoholic Steatohepatitis
Sponsor
Galectin Therapeutics Inc.
Enrollment
30
Locations
1
Primary Endpoint
Mean Change in Liver Fibrosis of Corrected T1 (cT1) Mapping (LiverMultiScan -LMS)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

A Randomized, Controlled, Double-blind, Parallel Group, Single Center Phase 2 Clinical Trial to Evaluate Multiple Non-Invasive Liver Fibrosis Imaging Methods in the Assessment of the Efficacy of GR-MD-02 for the Treatment of Liver Fibrosis in Patients with NASH with Advanced Fibrosis

Detailed Description

The primary objective is to determine the difference between placebo and GR-MD-02 treatment in the baseline adjusted mean change in liver fibrosis as measured by corrected T1 (cT1) mapping as determined from LiverMultiScan (LMS), a multi-parametric MRI protocol. Secondary objectives include evaluating differences between subjects treated with GR-MD-02 versus placebo in: * The baseline-adjusted change in liver stiffness as measured by MR-elastography * The baseline-adjusted change in liver stiffness as measured by FibroScan® scores. An exploratory objective will be to evaluate the correlation of the three diagnostic modalities of LiverMultiScan, MR-Elastography, and FibroScan®.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
September 27, 2016
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects must have liver biopsy demonstrating NASH with Brunt Stage 3 fibrosis within 12 months of randomization. The subject is ≥ 18 years of age and ≤ 75 years old at the time of screening
  • The subject is willing and able to provide written informed consent
  • The subject is not pregnant and must have a negative pregnancy test prior to start of the study. Post-menopausal women must have been amenorrheic for at least 12 months to be considered of non-child-bearing potential.
  • Fertile men and women participating in heterosexual relations must agree to use effective means of contraception throughout their participation in this study and for 90 days after discontinuation of study medication.
  • Lactating females must agree to discontinue nursing before the start of study treatment and refrain from nursing until 90 days after discontinuation of study medication.
  • Male subjects must refrain from sperm donation throughout the study period and for a period of 90 days following the last dose of study drug.

Exclusion Criteria

  • A history of hepatic decompensation including any episode of variceal bleeding, clinically detectable ascites, or overt hepatic encephalopathy.
  • Status post TIPS (Transjugular Intrahepatic Porto-systemic Shunt) procedure.
  • Evidence of other forms of chronic liver disease including viral hepatitis B or C, primary biliary cirrhosis, primary sclerosing cholangitis, Wilson's disease, alpha-1 antitrypsin deficiency, alcoholic hepatitis, hemochromatosis, liver cancer, or history of biliary diversion.
  • Any of the following laboratory values: Serum alanine aminotransferase (ALT) and aspartate aminotransferase levels \> 10X upper limits of normal, Serum creatinine ≥ 2.0 mg/dL, Platelet count \< 60,000/mm3, Serum albumin ≤ 2.8 g/dL, INR ≥ 1.7, Direct bilirubin ≥ 2.0 mg/dL
  • A MELD score ≥ 15 or Child-Pugh-Turcotte Stage B or C
  • Known positivity for Human Immunodeficiency Virus (HIV) infection
  • Any subject who had major surgery within 8 weeks of Day 1, significant traumatic injury, or anticipation of need for major surgical procedure during the course of the study.
  • Weight reduction surgery within the past 3 years.
  • Any subject with current, significant alcohol consumption or a history of significant alcohol consumption for a period of more than 3 consecutive months any time within 1 year prior to screening will be excluded.
  • Any subject with concurrent infection including diagnoses of fever of unknown origin (FUO) (subjects must be afebrile at the start of therapy).

Arms & Interventions

GR-MD-02

Active

Intervention: GR-MD-02

Placebo

Placebo

Intervention: Placebo

Outcomes

Primary Outcomes

Mean Change in Liver Fibrosis of Corrected T1 (cT1) Mapping (LiverMultiScan -LMS)

Time Frame: 16 weeks

Difference in baseline adjusted mean change in liver fibrosis of corrected T1 (cT1) mapping with LiverMultiScan (LMS). LiverMultiScan is CE marked as a class IIa medical device. Corrected T1 (cT1) is a Magnetic Resonance (MR) relaxation parameter/measure from the device.The measure cT1 can be compared across different Magnetic Resonance Imaging (MRI) systems and sites. It is an emerging biomarker for rapid quantification of hepatic fibro-inflammatory disease. In unhealthy tissue, such as in inflamed and fibrotic tissues, measures result in longer cT1-relaxation.

Secondary Outcomes

  • Baseline-adjusted Change in Liver Stiffness With MR-elastography (MRE)(16 weeks)
  • Baseline-adjusted Change in Liver Stiffness by FibroScan®(16 weeks)

Study Sites (1)

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