Skip to main content
Update Location

My Location

Update your location to show providers, locations, and services closest to you.

Enter a zip code
Or
Select a campus/region

Effects of NNC0194-0499, cagrilintide, and semaglutide alone or in combinations on liver damage and alcohol use in people with alcohol-related liver disease

  • Status
    Accepting Candidates
  • Age
    21 Years - NA Years
  • Sexes
    All
  • Healthy Volunteers

Description

We are doing this study to look at the effects of NNC0194-0499 (alone and in fixed-dose combination with semaglutide), cagrilintide (alone and in fixed-dose combination with semaglutide called CagriSema) and semaglutide (alone), on liver damage and alcohol use in people with Alcoholic Liver Disease. The study will include people with history of alcohol overuse and scar tissue build up in the liver. The study will last about 39 weeks.

Details

Protocol number 1380458

Eligibility

Women cannot take part if pregnant, breast-feeding or plan to get pregnant during the study period. Women who are able to become pregnant must use highly effective birth control throughout the study and will be counselled on the use of birth control. You cannot take part if you currently have infectious hepatitis or HIV.

Lead researcher

Participate in a study

Here are some general steps to consider when participating in a research study:

  1. Step
    1

    Contact the research team

    Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.

    Primary contact

  2. Step
    2

    Get screened to confirm eligibility

    You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.

  3. Step
    3

    Provide your consent to participate

    If you are eligible and want to join the clinical trial or study, a member of the research team will ask for your consent to participate. To give consent, you will be asked to read and sign a consent form for the study. This consent form explains the study's purpose, procedures, risks, benefits and provides other important information, such as the study team's contact information.

  4. Step
    4

    Participate

    If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.