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Be Part of Research - Trial Details - Research Study on Whether Semaglutide Works in People With Non-alcoholic Steatohepatitis (NASH)

Research Study on Whether Semaglutide Works in People With Non-alcoholic Steatohepatitis (NASH)

Medical Conditions

Fatty Liver
Non-alcoholic Fatty Liver Disease


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Semaglutide is a medicine studied in patients with NASH. Semaglutide is a well-known medicine, which is already used by doctors to treat type 2 diabetes in many countries.

Participants will either get semaglutide or a dummy medicine - which treatment participants get is decided by chance.

Participants will need to inject themselves with medicine under the skin. Participants will need to do this once a week.

The study will last for about 5 years. Participants will have up to 21 clinic visits and 9 phone calls with the clinical staff during the study. Some of the clinic visits may be spread over more than one day.

Participants with other chronic liver diseases cannot take part in this study. Women cannot take part in the study if they are pregnant, breast-feeding or plan to become pregnant during the study period.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Apr 2021 Apr 2029

Publications

"Newsome PN, Sanyal AJ, Engebretsen KA, Kliers I, Ostergaard L, Vanni D, Bugianesi E, Rinella ME, Roden M, Ratziu V. Semaglutide 2.4 mg in Participants With Metabolic Dysfunction-Associated Steatohepatitis: Baseline Characteristics and Design of the Phase 3 ESSENCE Trial. Aliment Pharmacol Ther. 2024 Dec;60(11-12):1525-1533. doi: 10.1111/apt.18331. Epub 2024 Oct 16."; "39412509"

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Semaglutide administrated subcutaneously (under the skin) once weekly there will be a period of dose escalation before reaching the target dose.

Intervention Arm Group : Semaglutide OW (once weekly );

Intervention Type : DRUG
Intervention Description : Placebo administrated subcutaneously (under the skin) once weekly.

Intervention Arm Group : Placebo;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Ninewells Hospital
    Dundee
    DD1 9SY
  • Southampton General Hospital
    Southampton
    SO16 6YD
  • John Radcliffe Hospital
    Oxford
    OX3 9DU
  • Royal Derby Hospital
    Derby
    DE22 3NE
  • Chelsea & Westminster Hospital
    London
    SW10 9NH
  • Imperial College London
    London
    W2 1NY
  • Nottingham University Hospital
    Nottingham
    NG7 2UH
  • St. James University Hospital
    Leeds
    LS9 7TF
  • New Queen Elizabeth Hospital Birmingham
    Birmingham
    B15 2TH
  • Joint Clinical Research Facility - Swansea
    Swansea
    SA2 8PP
  • Hull Royal Infirmary_Hull
    Hull
    HU3 2GZ
  • The Diabetes Centre
    Ipswich
    IP4 5RH
  • Royal Free - Immunity & Transplantation
    London
    NW3 2QG
  • Freeman Hospital, Newcastle
    Newcastle-Upon Tyne
    NE7 7DN
  • Royal Devon University Healthcare NHS Foundation Trust
    Exeter
    EX2 5DW
  • Freeman Hospital, Newcastle
    Newcastle upon Tyne
    NE7 7DN
  • Derriford Hospital
    Plymouth
    PL6 8DH


The study is sponsored by Novo Nordisk A/S




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Read full details for Trial ID: NCT04822181
Last updated 28 March 2025

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