Non-Alcoholic Fatty Liver Disease, the Hepatic Response to Oral Glucose, and the Effect of Semaglutide (NAFLD HEROES)

Who is this study for? Patients with non-alcoholic fatty liver disease
What treatments are being studied? Semaglutide
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Background: In non-alcoholic fatty liver disease (NAFLD), fat accumulates in the liver and can cause damage. Researchers want to learn what causes the damage NAFLD, and to see if a medication can help.

Objective: To find out how the liver in people with NAFLD responds to feeding, and how this relates to their response to the drug semaglutide.

Eligibility: People with NAFLD and healthy volunteers ages 18 and older

Design: Participants will be screened with: Medical history Physical exam Blood tests Imaging: A machine will take pictures of the participant s body. Within 2-8 weeks of enrollment, participants will stay in the clinic for several days. This includes: Blood, urine, heart, and imaging tests For NAFLD participants only: A needle-like device will remove a small biopsy of the liver and fatty tissue. Participants will be alone in a special room for 5 hours. They will breathe through a tube under the nostrils. They will have blood drawn several times. The baseline visit concludes participation for healthy volunteers but NAFLD participants will contine. About 6 weeks after discharge, participants will stay in the clinic again and repeat the tests. They will get their first semaglutide dose by injection. Participants will have visits weeks 1, 2, 4, 8, 12, 16, 20, and 24 of treatment. Visits include blood tests. Participants will inject semaglutide once a week at home. At week 30, participants will stay in the clinic again and repeat the tests. Participants will have a final visit 12 weeks after stopping treatment. This includes blood and urine tests. ...

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: t
View:

• Male or female Aged greater than or equal to 18 years of age.

• No evidence of hepatic steatosis by imaging or histology.

• No history of known liver disease.

• Individuals on regular systemic medications may be considered eligible, and their eligibility will be determined by the principal investigator.

• BMI less than or equal to 25 kg/m2

• Non-diabetic.

• Normal transaminases (ALT less than or equal to 31 U/L for men or less than or equal to 19 U/L for women, and AST less than or equal to 30 U/L).

• Fasting glucose less than or equal to 95 mg/dL.

• Ability of subject to understand and the willingness to sign a written informed consent document.

Locations
United States
Maryland
National Institutes of Health Clinical Center
RECRUITING
Bethesda
Contact Information
Primary
Yaron Rotman, M.D.
rotmanyaron@mail.nih.gov
(301) 451-6553
Time Frame
Start Date: 2019-07-24
Estimated Completion Date: 2026-10-02
Participants
Target number of participants: 84
Treatments
Experimental: Arm A: Steatosis
Participants with steatosis on baseline biopsy
Experimental: Arm B: NASH
Participants with NASH on baseline biopsy
No_intervention: Arm C: Healthy
Healthy Volunteers
Related Therapeutic Areas
Sponsors
Collaborators: National Cancer Institute (NCI)
Leads: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

This content was sourced from clinicaltrials.gov