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Recruiting

NCT Number: NCT05018481

HA35 Moderate Alcoholic Hepatitis (AH) Study

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.

Recruiting

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Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Location status: Recruiting

Location contact

Annette Bellar

CONTACT

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of alcoholic hepatitis defined as:
  • Regular consumption of alcohol with an intake of >60 g daily or >420 g weekly on average for men and >40 g daily or >280 g weekly on average for women for 6 months or 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 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 Institute Withdrawal 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 alcoholic liver 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 blood clotting

Treatment and study plan

Sodium Hyaluronate

Drug

Sodium hyaluronate of molecular weight 35kDa will be given in capsule form to study participants

Other names: HA35

Placebo

Drug

A placebo will be given in capsule form to study participants

Primary outcomes

  1. Compare percent change of skeletal muscle mass

    Time frame: Baseline to 90 days

Study contacts

Contact information is provided by the study sponsor or research team.

Annette Bellar

CONTACT

[email protected]

Srinivasan Dasarathy, MD

CONTACT

[email protected]

216-318-7010

Sponsors and collaborators

Lead sponsor

The Cleveland Clinic

Other

Registry information

Official study title

Mechanism of HA35 in Patients With Alcoholic Liver Disease

Important dates

Study start
2022
Primary completion
2026
Study completion
2027
First posted
Aug 24, 2021
Registry last updated
Nov 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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