Ph 2 Study of the Safety and Efficacy of Three HU6 Dose Levels and Placebo in Nonalcoholic Steatohepatitis

April 16, 2024 updated by: Rivus Pharmaceuticals, Inc.

A 6-Month, Randomized, Double-Blind, Placebo-controlled, Phase 2 Study of the Safety and Efficacy of Three HU6 Dose Levels and Placebo in Nonalcoholic Steatohepatitis

This is a phase 2 randomized, double-blind, placebo-controlled parallel group study of 3 dose levels of HU6 in subjects with nonalcoholic steatohepatitis (NASH). Six months (26 weeks) of dosing is planned, and subjects will be followed for safety, efficacy, pharmacodynamics (PD), and pharmacokinetics (PK) during this time. The end-of-study visit will take place approximately 4 weeks after the last dose of the study drug (Week 30).

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This is a phase 2 randomized, double-blind, placebo-controlled parallel group study of 3 dose levels of HU6 (150 mg, 300 mg, and 450 mg) and placebo in approximately 204 subjects with NASH.

Subjects will be screened over a 49-day period to determine their eligibility based on specific history, physical, laboratory, and imaging evaluations, which will require more than one visit during the screening period. On Day 1, subjects will be randomized 2:1:2:2 into 1 of 4 treatment groups (placebo, 150 mg HU6, 300 mg HU6, or 450 mg HU6). Six months (26 weeks) of dosing is planned, and subjects will be followed for safety, efficacy, PD, and PK during this time. The end-of-study visit will take place approximately 4 weeks after the last dose of the study drug (Week 30).

Study Type

Interventional

Enrollment (Estimated)

204

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • United States
    • California
      • Chula Vista, California, United States, 91911
      • Los Angeles, California, United States, 90057
      • Montclair, California, United States, 91763
      • Sacramento, California, United States, 95821
        • Recruiting
        • Northern California Research Center
        • Contact:
        • Principal Investigator:
          • Douglas Young, MD
      • San Bernardino, California, United States, 92404
        • Recruiting
        • Metro Clinical Trials
        • Principal Investigator:
          • Cecilia Casaclang, MD
        • Contact:
    • Florida
      • Bradenton, Florida, United States, 34208
      • Cape Coral, Florida, United States, 33914
        • Recruiting
        • ABMED Clinical Research Corp.
        • Contact:
        • Principal Investigator:
          • Paige Kreegel, MD
      • Fort Myers, Florida, United States, 33907
        • Recruiting
        • Southwest General Healthcare Center
        • Principal Investigator:
          • Jose Rodriguez, MD
        • Contact:
        • Contact:
      • Miami, Florida, United States, 33155
      • Miami, Florida, United States, 33176
      • Miami, Florida, United States, 33173
      • Miami, Florida, United States, 33156
      • Miami Lakes, Florida, United States, 33014
        • Recruiting
        • Panax Clinical Research
        • Principal Investigator:
          • Robert Perry, MD
        • Contact:
        • Contact:
    • Louisiana
    • New Jersey
      • Berlin, New Jersey, United States, 08009
        • Recruiting
        • CenExel HRI
        • Principal Investigator:
          • Michael Hassman, MD
        • Contact:
        • Contact:
    • North Dakota
      • Fargo, North Dakota, United States, 58104
    • Texas
      • Austin, Texas, United States, 78745
        • Recruiting
        • IMA Clinical Research-Austin
        • Contact:
        • Principal Investigator:
          • Kim Nomita, MD
      • Houston, Texas, United States, 77079
      • Houston, Texas, United States, 77030
      • San Antonio, Texas, United States, 78215
        • Recruiting
        • Texas Liver Institute
        • Principal Investigator:
          • Eric Lawitz, MD
        • Contact:
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Able to understand the procedures and requirements of the study and provide written informed consent and authorization for protected health information disclosure.
  2. Willing and able to comply with the requirements of the study protocol.
  3. Male or female ≥18 years of age at time of informed consent.
  4. Subject has a screening Fibroscan® CAP score >306 decibels per meter (dB/m) and interquartile range to median ratio (IQR/Med) <30%.
  5. Subject has ≥8% liver fat determined by screening Magnetic Resonance Imaging Proton Density Fat Fraction (MRI-PDFF).
  6. Subject has moderate to advanced liver fibrosis based on documented history of biopsy score of F2 or F3 within 12 months prior to Screening, or subject has a screening Fibroscan® vibration-controlled transient elastography (VCTE) score ≥ 7.0 to ≤ 15.0 kPa.
  7. Body mass index (BMI) ≥27.0 kg/m2.
  8. Clinically euthyroid as assessed by a thyroid profile utilizing TSH and T4 testing at screening as assessed by the investigator based on the medical history of the subject.
  9. Subjects with a diagnosis of glaucoma must be controlled and stable (no changes in treatment regimen within 3 months prior to Screening).
  10. Inclusion as per investigator assessment of general medical status and as documented by medical history, physical examination, vital sign assessments, 12-lead ECG, clinical laboratory assessments, and general observations.

Exclusion Criteria:

Subjects will be excluded from the study if any of the following criteria are met:

  1. The subject has a history of cirrhosis and/or hepatic decompensation, including ascites, hepatic encephalopathy, or variceal bleeding.
  2. The subject has a history of acute pancreatitis within 1 year of Screening or chronic pancreatitis of any cause.
  3. History of any bariatric surgery intervention, including but not limited to lap banding, intragastric balloon, duodenal-jejunal sleeve, or bariatric surgery or plans for bariatric surgery prior to conclusion of study participation.
  4. Have obesity induced by other endocrinologic disorders (e.g., Cushing Syndrome, polycystic ovarian syndrome) or diagnosed monogenetic or syndromic forms of obesity (e.g., Melanocortin 4 Receptor deficiency or Prader-Willi Syndrome).
  5. Any surgical or medical condition or history that, in the opinion of the investigator in consultation with the medical monitor, may potentially alter the absorption, metabolism, or excretion of study treatment.
  6. History of or treatment for clinically significant gastroparesis, inflammatory bowel disease, or any surgery of the upper gastrointestinal tract with the exception of cholecystectomy, or minor gastric procedures that are approved by the medical monitor.
  7. History (including any family history) of malignant hyperthermia.
  8. History of chronic serious recurrent skin rashes of unknown cause.
  9. History of malignancy within 5 years (except cutaneous basal or squamous cell carcinoma, carcinoma-in-situ, or low-grade prostate cancer).
  10. History of the following cardiovascular conditions within 3 months prior to randomization: acute myocardial infarction, cerebrovascular accident (stroke), unstable angina, hospitalization due to congestive heart failure (CHF), or acute CHF.
  11. NYHA Functional Class II, III, or IV heart failure.
  12. Subject has a pacemaker.
  13. Active kidney disease requiring therapy, kidney transplant, or eGFR <45 mL/min/1.73 m2 based on the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) Creatinine Equation.
  14. Significant and unstable lung disease (chronic obstructive pulmonary disease [COPD], emphysema, pulmonary fibrosis, or asthma) requiring oxygen or chronic daily medication. Note that mild, stable COPD and asthma on inhalers are allowed.
  15. Subject has a diagnosed history of obstructive sleep apnea or uses continuous positive airway pressure (CPAP).
  16. Subject has a history of ketoacidosis or hyperosmolar state requiring hospitalization in the 6 months prior to Screening.
  17. Subject has any history of agranulocytosis.
  18. Subject has Wilson's disease.
  19. Familial (mother/father/sibling) and/or personal history of retinal detachment any time in the past.
  20. Subject has history of prior vitrectomy due to prior retinal condition.
  21. Subject has a contraindication to dilation for ophthalmologic examination.

  22. Evidence of the following on screening ophthalmologic examination:

    1. Peripheral retinal pathology, retinal tears, lattice, or nondiabetic ocular condition that requires treatment or intervention within 3 months of Screening.
    2. Diabetic retinopathy with macular exudates or macular edema (evidence of microaneurysms is not an exclusion).
    3. Any active macular disease that affects the vision, including macular pucker (epiretinal membrane), retinal vein occlusion, and macular degeneration.
    4. Subjects with significant visual impairment due to lens opacity from cataracts such that surgery will be required within the duration of the study in the opinion of the consulting ophthalmologist. (Subjects with cataract surgery >3 months prior to Screening may be included.)
    5. Subject has substantial media opacities that preclude successful retinal imaging.
  23. Any condition (e.g., ongoing substance, drug, or alcohol abuse) that may interfere with participation or safety of investigations, in the opinion of the Investigator.
  24. A history of moderate alcohol consumption defined as drinking ≥ 2 drinks per day for men or ≥ 1 drink per day for women. (A drink is defined as 12 ounces of beer, 5 ounces of wine, 1.5 ounces of distilled spirits.).
  25. Subjects with untreated, uncontrolled, or unstable hypertension (systolic blood pressure [SBP] >160 and/or diastolic blood pressure [DBP] >100 mmHg upon repeat evaluation at screening). If subject is treated with antihypertensive medication, the regimen must be stable at least 1 month prior to screening.
  26. Subjects with untreated or persistent hypotension (SBP <90 mmHg) or symptomatic hypotension (that, in the opinion of the Investigator, requires active treatment).
  27. Tachycardia (>100 beats/minute) at screening.
  28. QTcF > 450 msec at screening for males and QTcF > 470 msec at screening for females.

  29. Use of any of the following medications:

    1. The following oral antidiabetic drugs are prohibited within 3 months prior to screening and continuing throughout the study: insulin, meglitinides, thiazolidinediones, glucagon-like peptide (GLP-1) agonists, and gastric inhibitory polypeptide (GIP)/GLP-1 agonists.
    2. The following are prohibited within 3 months prior to screening (or planned use during the study) when used for weight loss: herbal preparation, over the counter (OTC) drug, mail order or prescription drug.
    3. Prescription or OTC stimulants including: dextroamphetamine/Dexedrine, dextroamphetamine/amphetamine combination product/Adderall, or methylphenidate (Ritalin®, Concerta®).
    4. Recent (within 3 months of screening) or current use of obeticholic acid/Ocaliva, systemic corticosteroids, methotrexate, tamoxifen, amiodarone, or long-term use of tetracyclines.
    5. Warfarin, heparin, factor Xa inhibitors (e.g., dabigatran, betrixaban, edoxaban, apixaban, and rivaroxaban).
    6. Vitamin E: use of ursodiol or high-dose vitamin E (>400 IU/day) for at least 1 month within the previous 6 months or started high dose vitamin E within the previous 3 months of Screening.
    7. Drugs with high risk of idiosyncratic drug-induced neutropenia (IDIN) or agranulocytosis (Andres 2018, Curtis 2017): antithyroid drugs (propylthiouracil and methimazole), ticlopidine, clozapine, phenothiazines, sulfasalazine, vancomycin, amoxicillin, ceftriaxone, ciprofloxacin, cotrimaxozole, piperacillin-tazobactam, and trimethoprim-sulfamethoxazole (Bactrim® or Septra®).
    8. Concomitant medications that prolong the QT/QTc interval and are known to be associated with increased risk of Torsade des pointes as identified in the https://crediblemeds.org/ website list category of 'Known Risk.'

  30. Have acute or chronic hepatitis, signs, and symptoms of any other liver disease other than nonalcoholic fatty liver disease (NAFLD)/NASH, or any of the following, as determined by the central laboratory during screening:

    1. International normalized ratio (INR) ≥1.3, or
    2. ALT >5.0× the ULN for the reference range, or
    3. AST >5.0× the ULN for the reference range, or
    4. Alkaline phosphatase (ALP) >2.0× the ULN for the reference range, or
    5. Total bilirubin >1.2× the ULN for the reference range (except for cases of known Gilbert's Syndrome).

  31. Laboratory Values at Screening:

    1. Hemoglobin <9.5 g/dL, or
    2. ANC ≤1500/μL, or
    3. Marked hypertriglyceridemia (>1000 mg/dL), or
    4. Copper <LLN for the reference range, or
    5. Ceruloplasmin <LLN for the reference range, or
    6. Serologic evidence of hepatitis B based on hepatitis B surface antigen (HBsAG), or
    7. Serologic evidence of hepatitis C antibody (HCV Ab) and HCV RNA, or
    8. Serologic evidence of human immunodeficiency virus (HIV).
    9. Hemoglobin A1c (HbA1c) > 9.5%.

  32. Intolerance to MRI or with conditions contraindicated for MRI procedures including but not limited to:

    1. Having surgical clips/metallic implants/shrapnel -or-
    2. Claustrophobia, have a history of claustrophobia, or intolerance of closed or small spaces.
  33. Participation in another clinical trial at the time of screening or exposure to any investigational agent, including topical agents, within 30 days or 5 half-lives prior to Day 1, whichever is longer.
  34. For subjects with a recent active viral, bacterial, or parasitic infection, they must have discontinued any treatment for their infection at least 5 days prior to screening. Patients who test positive for COVID-19 during the screening period must have a negative rapid antigen test prior to randomization.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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: Active Treatment: HU6 Planned doses of HU6
Drug: HU6
HU6 is being evaluated for its efficacy in improving liver fat content in subjects with Nonalcoholic Steatohepatitis (NASH)
Placebo Comparator: Placebo Comparator Non-active study drug
Other: Placebo
Placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Percent change from baseline in liver fat, as assessed by magnetic resonance imaging liver proton density fat fraction (MRI-Liver PDFF) at 6 months (26 weeks)
Time Frame: 6 months
6 months

Secondary Outcome Measures

Outcome Measure
Time Frame
Percent change from baseline in body weight at 6 months (26 weeks)
Time Frame: 6 months
6 months
Change from baseline in HbA1c at 6 months (26 weeks).
Time Frame: 6 months
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Rivus Pharmaceuticals, Inc.

Investigators

  • Study Director: Rob Schott, MD, Rivus Pharmaceuticals, Inc.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 5, 2023

Primary Completion (Estimated)

February 1, 2025

Study Completion (Estimated)

April 1, 2025

Study Registration Dates

First Submitted

July 31, 2023

First Submitted That Met QC Criteria

July 31, 2023

First Posted (Actual)

August 7, 2023

Study Record Updates

Last Update Posted (Actual)

April 17, 2024

Last Update Submitted That Met QC Criteria

April 16, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RIV-HU6-2202

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

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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