HA35 Moderate Alcoholic Hepatitis (AH) Study

Last updated: January 8, 2025
Sponsor: The Cleveland Clinic
Overall Status: Active - Recruiting

Phase

1

Condition

Hepatitis

Liver Disorders

Treatment

Sodium Hyaluronate

Placebo

Clinical Study ID

NCT05018481
21-605
  • Ages 21-65
  • All Genders

Study Summary

Eligible participants will be asked to take a placebo/treatment capsule for 90 days and participate in two in-person study visits, one at the start of the 90 days and the second at the completion of study supplement administration. Both visits will include a physical exam, clinical labs, body composition measurements, muscle strength tests, questionnaires, and urine and stool collections. Additionally, a sugar cocktail will be consumed to measure gut permeability and a muscle biopsy will be collected. The day after the visits, you will need to return to drop off the 24-hour urine collection.

Two phone visits will be performed in between the in-person visits at day 30 and 60 where you will be asked a series of questionnaires as well as asked about study supplement compliance.

Eligibility Criteria

Inclusion

Inclusion Criteria:

• Clinical diagnosis of alcoholic hepatitis defined as:

  • Regular consumption of alcohol with an intake of >60 g daily or >420 g weekly onaverage for men and >40 g daily or >280 g weekly on average for women for 6 monthsor more

AND

  • MELD <21

  • Serum total bilirubin >3 mg/dL

  • AST >50 IU/I; AST:ALT ratio >1.5; Both AST and ALT <400 IU/I

OR Histologic evidence of AH.

Exclusion

Exclusion Criteria:

  • Pregnant or breastfeeding women

  • Patients with gastrointestinal bleeding within 2 weeks

  • Active infection (positive blood or ascitic fluid culture)

  • Overt encephalopathy

  • Renal failure and/or on dialysis

  • Medications that alter muscle protein metabolism

  • Myopathies

  • Other end-stage organ diseases

  • Malignancy

  • Solid organ or hematopoietic transplantation

  • Active alcohol withdrawal or ongoing participation in a Clinical InstituteWithdrawal Assessment (CIWA) protocol

  • History of recent upper gastrointestinal resection within past 6 months

  • Acute or chronic liver disease due to other active causes, in addition to alcoholicliver disease

  • Inability to provide consent

  • Creatinine >2mg/dL

  • Platelets <60,000k/ul

  • PT/INR >1.7

  • Presence of pedal edema

  • Use of anti-platelet/anticoagulation drugs or medications that interfere with bloodclotting

Study Design

Total Participants: 54
Treatment Group(s): 2
Primary Treatment: Sodium Hyaluronate
Phase: 1
Study Start date:
September 01, 2022
Estimated Completion Date:
October 01, 2026

Study Description

Written informed consent will be obtained during the baseline visit (day 1). Patients will given a physical exam and a blood test will be obtained if not in their medical chart. The subjects who meet the criteria after the screening visit will have the following procedures: A. Body composition will be quantified by whole-body dual energy X-ray absorptiometry (DEXA), Bioelectric Impedance Analysis (BIA), chair stands, 3 position balance and hand grip strength by dynamometry. B. Muscle biopsy from the lateral portion of vastus lateralis, about 20 cm above knee, C. Questionnaires, D. Blood collection, E. Collection of stool samples, F. Sugar cocktail administration, and G. Urine collection (24 hour)

After baseline measures have been completed, patients will be randomized in a 1:1 ratio to either standard of care (SOC) + HA35 or SOC + placebo (140 mg/d) for a total of 3 months post enrollment.

The subjects will be recalled after 3 months. The visit and the procedures conducted on day 90 will be similar to the baseline study visit.

Connect with a study center

  • Cleveland Clinic

    Cleveland, Ohio 44195
    United States

    Active - Recruiting

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