- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05402371
A Study to Evaluate the Efficacy and Safety of Rencofilstat in Subjects With NASH and Advanced Liver Fibrosis (ASCEND)
A Phase 2B, Randomized, Multi-Center, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Rencofilstat in Adult Subjects With Nonalcoholic Steatohepatitis and Advanced Liver Fibrosis
Study Overview
Status
Intervention / Treatment
Detailed Description
This is a randomized, double-blind, placebo-controlled, parallel-dosing, multi-center study to evaluate the efficacy and safety of Rencofilstat as evidenced by histopathological improvements in fibrosis in adult NASH subjects with F2 or F3 fibrosis (NASH CRN system). Antifibrotic biomarker activity will be evaluated on an exploratory basis.
This study consists of 3 phases: (i) Screening and Randomization; (ii) treatment; and (iii) follow up. During Screening, each subject will provide informed consent prior to starting any study specific procedures. The randomization of the F2/F3 NASH subjects will be performed in a 1:1:1:1 ratio between Rencofilstat 75mg, Rencofilstat 150mg, Rencofilstat 225mg, and matching placebo. Subjects will be stratified by presence or absence of Type 2 diabetes, fibrosis stage and a maximum of 34 F2 subjects in each cohort.
Study Type
Enrollment (Anticipated)
Phase
- Phase 2
Contacts and Locations
Study Contact
- Name: Kristen Fetchko
- Phone Number: 732-902-4000
- Email: ascendnashstudy@hepionpharma.com
Study Locations
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Pessac, France, 33604
- Recruiting
- Hôpital du Haut Lévêque
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Contact:
- Hepion Investigator
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Mexico City, Mexico, 06700
- Recruiting
- Centro de Investigacion y Gastroenterologia SC
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Contact:
- Hepion Investigator
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Alabama
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Huntsville, Alabama, United States, 35801
- Recruiting
- Medical Affiliated Research Center
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Contact:
- Hepion Investigator
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Arizona
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Chandler, Arizona, United States, 85224
- Recruiting
- Arizona Liver Health-Chandler
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Contact:
- Hepion Investigator
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Peoria, Arizona, United States, 85381
- Recruiting
- Arizona Liver Health
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Contact:
- Hepion Investigator
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Tucson, Arizona, United States, 85712
- Recruiting
- Adobe Clinical Research, LLC
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Contact:
- Hepion Investigator
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Tucson, Arizona, United States, 85712
- Recruiting
- Arizona Liver Health-Tuscon
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Contact:
- Hepion Investigator
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Arkansas
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Little Rock, Arkansas, United States, 72211
- Recruiting
- Preferred Research Partners, Inc.
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Contact:
- Hepion Investigator
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North Little Rock, Arkansas, United States, 72117
- Recruiting
- Arkansas Gastroenterology
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Contact:
- Hepion Investigator
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California
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Huntington Park, California, United States, 90255
- Recruiting
- National Research Institute
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Contact:
- Hepion Investigator
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Los Angeles, California, United States, 90057
- Recruiting
- National Research Institute
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Contact:
- Hepion Investigator
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Panorama City, California, United States, 91402
- Recruiting
- National Research Institute
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Contact:
- Hepion Investigator
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Santa Ana, California, United States, 92704
- Recruiting
- National Research Institute
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Contact:
- Hepion Investigator
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Florida
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Bradenton, Florida, United States, 34208
- Recruiting
- Synergy Healthcare, LLC
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Contact:
- Hepion Investigator
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Clearwater, Florida, United States, 33761
- Recruiting
- Tampa Bay Medical Research, Inc.
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Contact:
- Hepion Investigator
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Cutler Bay, Florida, United States, 33189
- Recruiting
- Top Medical Research, Inc.
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Contact:
- Hepion Investigator
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Doral, Florida, United States, 33166
- Recruiting
- Integrity Clinical Research, LLC
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Contact:
- Hepion Investigator
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Hialeah Gardens, Florida, United States, 33016
- Recruiting
- Evolution Clinical Trials, Inc.
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Contact:
- Hepion Investigator
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Jacksonville, Florida, United States, 32256
- Recruiting
- Borland Groover Clinical Research
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Contact:
- Hepion Investigator
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Lady Lake, Florida, United States, 32159
- Recruiting
- Ocala GI Research
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Contact:
- Hepion Investigator
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Lakeland, Florida, United States, 33803
- Recruiting
- Accel Research Sites-Lakeland CRU
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Contact:
- Hepion Investigator
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Miami, Florida, United States, 33165
- Recruiting
- Future Care Solutions, LLC
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Contact:
- Hepion Investigator
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Miami, Florida, United States, 33176
- Recruiting
- Entrust Clinical Research
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Contact:
- Hepion Investigator
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Miami, Florida, United States, 33186
- Recruiting
- United Reseach Group
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Contact:
- Hepion Investigator
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Orlando, Florida, United States, 32810
- Recruiting
- Omega Research Consultants, LLC
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Contact:
- Hepion Investigator
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Port Orange, Florida, United States, 32127
- Recruiting
- Progressive Medical Research
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Contact:
- Hepion Investigator
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Sarasota, Florida, United States, 34240
- Recruiting
- Covenant Research and Clinics
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Contact:
- Hepion Investigator
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Georgia
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Dalton, Georgia, United States, 30720
- Recruiting
- Southeast Clinical Research Center
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Contact:
- Hepion Investigator
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Marietta, Georgia, United States, 30060
- Recruiting
- Gastrointestinal Specialists of Georgia, PC
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Contact:
- Hepion Investigator
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Indiana
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South Bend, Indiana, United States, 46635
- Recruiting
- Digestive Research Alliance of Michiana, LLC
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Contact:
- Hepion Investigator
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Louisiana
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Bastrop, Louisiana, United States, 71220
- Recruiting
- Delta Research Partners
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Contact:
- Hepion Investigator
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Maryland
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Greenbelt, Maryland, United States, 20770
- Recruiting
- Mid-Atlantic GI Research, LLC
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Contact:
- Hepion Investigator
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New Jersey
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Florham Park, New Jersey, United States, 07932
- Recruiting
- AIG Digestive Disease Research, LLC
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Contact:
- Hepion Investigator
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Texas
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Austin, Texas, United States, 78757
- Recruiting
- Pinnacle Clinical Research-Austin
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Contact:
- Hepion Investigator
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Brownsville, Texas, United States, 78520
- Recruiting
- South Texas Research Institute
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Contact:
- Hepion Investigator
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Edinburg, Texas, United States, 78539
- Recruiting
- South Texas Research Institute
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Contact:
- Hepion Investigator
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Pearland, Texas, United States, 77584
- Recruiting
- Linq Research, Llc
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Contact:
- Hepion Investigator
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San Antonio, Texas, United States, 78229
- Recruiting
- Pinnacle Clinical Research-San Antonio
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Contact:
- Hepion Investigator
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Virginia
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Newport News, Virginia, United States, 23602
- Recruiting
- Bon Secours Liver Institute of Hampton Roads
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Contact:
- Hepion Investigator
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Richmond, Virginia, United States, 23236
- Recruiting
- GI Select Health Research, LLC
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Contact:
- Hepion Investigator
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Washington
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Spokane, Washington, United States, 99202
- Recruiting
- Velocity Clinical Spokane
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Contact:
- Hepion Investigator
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria Subjects must fulfill all the following inclusion criteria to be eligible for participation in the study.
- Male or female between 18 and 75 years of age (inclusive).
- Capable of giving written informed consent and able to effectively communicate with the investigator and study personnel.
Histologic evidence of NASH based on central readings of the screening biopsy obtained no more than 6 months before Screening defined by presence of all 3 key histological features, Nonalcoholic Fatty Liver Disease Activity Score (NAS) ≥ 4 with at least 1 point each in lobular inflammation and hepatocyte ballooning.
a. Historical biopsy may be substituted for Screening biopsy to determine eligibility if the following are met: i. Historical biopsy was obtained no more than 180 ± 5 days prior to the first day of Screening.
ii. Hepatic tissue or slides are available for central histologic evaluation. iii. No new therapeutic intervention for NASH was made 90 days prior to screening (e.g., obeticholic acid, vitamin E ≥ 400 IU/day, pioglitazone, incretins [e.g., liraglutide, semaglutide], sodium-glucose cotransporter-2 [SGLT2] inhibitors).
iv. Subjects must have been metabolically stable since the biopsy (no significant weight loss ≥ 7% of body weight, no major deterioration of glycemic control, and no introduction of new or investigational drugs for the treatment of Type 2 Diabetes).
- Histologic liver fibrosis stage 2 or 3 as defined by the Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) scoring of liver fibrosis based on central reading of the Screening biopsy (refer to criteria 4a regarding use of a historical biopsy as a substitute for the Screening biopsy).
- Blood pressure up to 160/100 mmHg; potential subjects who meet other eligibility requirements, but who have out of range blood pressure measurements deemed to be not clinically significant by the investigator, may still be considered for study inclusion.
Exclusion Criteria Subjects who meet any of the following criteria prior to the first dose of study drug are not eligible for randomization.
- Pregnant or breastfeeding or planning to become pregnant during the study period.
- Known allergy to Rencofilstat, cyclosporine, or any of their inactive ingredients.
- Positive test for hepatitis B surface antigen (HBsAg), hepatitis C virus antibodies (HCVAb) or human immunodeficiency virus antibodies (HIVAb). If HCVAb test is positive, then an HCV-RNA test will be performed. If this test is negative, the subject is allowed to participate in the study, as long as the subject meets all other inclusion criteria and has never been treated for HCV or was treated >2 years ago and achieved a sustained virologic response at that time.
- Subjects with suspected and symptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection identified prior to first dose.
- Subjects with a history of clinically significant acute cardiac events within 30 days prior to Screening such as stroke, transient ischemic attack, or coronary heart disease (angina pectoris requiring therapy, myocardial infarction, revascularization procedures with left ventricular ejection fraction [LVEF] <50% as determined by previous echocardiography or multiple gated acquisition [MUGA] scan).
Subjects with uncontrolled or unstable cardiac arrhythmias:
- Severe conduction disturbance (e.g., second-degree or third-degree AV block).
- History of congenital long QT syndrome, congenital short QT syndrome, Torsades de Pointes, or Wolff Parkinson White syndrome.
- Subjects with transaminases >5 x upper limit of normal (ULN).
- Subjects with ALP >2 x ULN.
- Subjects with total serum bilirubin >1.5 x ULN.
- Subjects with a platelet count <100,000/mm3.
- Subjects with an INR ≥ 1.3 in the absence of anticoagulants.
- Subjects with albumin <3.5 g/dL.
- Model for End-Stage Liver Disease (MELD) score >12, unless due to an alternate etiology such as therapeutic anticoagulation.
- Current or previous (within the past 6 months) Child-Pugh (CP) score ≥ 7 for F2 or F3 subjects, unless due to an alternative etiology such as Gilbert's syndrome or therapeutic anticoagulation.
- An estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2 (calculated by the Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI] method).
- Subjects with hemoglobin A1c (HbA1c) >9.5%.
- Subjects with any history or presence of decompensated cirrhosis including ascites, hepatic encephalopathy or variceal bleeding.
Other well documented causes of chronic liver disease according to standard diagnostic procedures including, but not restricted to:
- Suspicion of drug-induced liver disease.
- Alcoholic liver disease.
- Autoimmune hepatitis.
- Wilson's disease.
- Primary biliary cholangitis, primary sclerosing cholangitis.
- Genetic hemochromatosis (Homozygosity for C282Y or C282Y/H63D compound heterozygote).
- Known or suspected hepatocellular carcinoma (HCC).
- History or planned liver transplant.
- Clinical evidence of portal hypertension such as esophageal varices, ascites, history of hepatic encephalopathy, or splenomegaly.
- History of hepatic decompensating events or subjects who develop manifestations of hepatic decompensation between screening and enrollment should not be randomized, inclusive of new or worsening jaundice and ascites, new esophageal varices, etc.
- Subjects with Type 2 diabetes who have recent (< 3 months) changes in medication class or dose of the following antidiabetic medications: Glucagon-like-peptide-1 (GLP-1) receptor agonist, dipeptidyl peptidase-4 (DPP-4) inhibitor, sodium/glucose cotransporter 2 (SGLT2) inhibitor, thiazolidinediones (TZD).
- Received an investigational drug or investigational vaccine or used an investigational medical device within 60 days prior to first dose of study drug.
- Received any investigation products being evaluated for the treatment of liver fibrosis or NASH in the 6 months prior to the Screening liver biopsy.
- Inability to undergo MRE procedure due to unremovable metal or foreign object(s) or contraindication for any other reason including but not limited to pacemaker, shrapnel injury, extensive tattoos, severe claustrophobia, ear (cochlea) implant.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Cohort A: Rencofilstat 75 mg
Eighty-four (84) biopsy-proven NASH F2/F3 subjects to complete study on Rencofilstat 75 mg daily.
|
Rencofilstat soft gel capsule
Other Names:
|
Experimental: Cohort B: Rencofilstat 150 mg
Eighty-four (84) biopsy-proven NASH F2/F3 subjects to complete study on Rencofilstat 150 mg daily.
|
Rencofilstat soft gel capsule
Other Names:
|
Experimental: Cohort C: Rencofilstat 225 mg
Eighty-four (84) biopsy-proven NASH F2/F3 subjects to complete study on Rencofilstat 225 mg daily.
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Rencofilstat soft gel capsule
Other Names:
|
Placebo Comparator: Cohort D: Placebo
Eighty-four (84) biopsy-proven NASH F2 / F3 subjects to complete study on matching placebo.
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placebo soft gel capsule
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of subjects with improvement in fibrosis by at least 1 stage (NASH CRN system) OR NASH resolution without worsening of fibrosis.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
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Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of subjects with improvement in fibrosis by at least 1 stage (NASH CRN system), regardless of effect on NASH.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
|
Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Proportion of subjects with improvement in fibrosis by at least 2 stages (NASH CRN system), regardless of effect on NASH.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
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Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Proportion of subjects with improvement in fibrosis by at least 2 stages (NASH CRN system) AND no worsening of NASH.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
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Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Change from baseline in ALT.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
|
Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Change from baseline in AST.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
|
Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Change from baseline in Pro-C3, type III collagen neo-epitopes.
Time Frame: dosing period of 1 year with 1 month observation and follow up period
|
Efficacy
|
dosing period of 1 year with 1 month observation and follow up period
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Stephen Harrison, MD, Pinnacle Clinical Research
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HEPA-CRV431-207
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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