
Project Details
Start Date
August 2021
Status
Closed to Recruitment
Principal Investigator
Dr Tom Russ
NDN Study Lead
Jessica Crossan
Main Research Site
Western General Hospital
This clinical trial looks to see if the oral version of the medication semaglutide can help treat Alzheimer’s disease. The EVOKE and EVOKE Plus trials are similar, but are considered separate studies as people who also have cerebral vascular changes (heart conditions) will take part in the EVOKE Plus trial, instead.
What Happens In This Study?
You will either be given a medicine called semaglutide or a placebo (a dummy pill that looks like the medicine but has no active ingredients). Neither you, nor the research team, will know which group you are in.
Can I Join This Study?
To take part in this medical trial, you must meet these 8 requirements:
- Your Diagnosis: A doctor must have confirmed that you have MCI or mild dementia of the Alzheimer’s type.
- Your Age: You are between 55 and 85 years old.
- Your Symptoms: Your symptoms should be mild or moderate. A doctor will be able to assess your symptom severity.
- Your Current Medicine: If you are taking Alzheimer’s disease medication, you must have been taking this for at least 3 months, without making any big changes to it.
- Your Study Partner: You must have a reliable friend of family member who knows you well and you see regularly, who can also take part to provide us with information on how you are doing.
- Your Permission: You must be able to understand what happens in the study and sign a form (called informed consent) to say you agree to join.
- Your Time: You must do your best to attend all your study visits, and follow the rules of the study until it ends.
- Taking the Medicine: You must be willing and able to swallow the trial medication.
Study Length: 104 weeks (2 years), with an optional extension of 52 weeks (1 year)
Number of appointments: 13 visits, with an optional extension of 5 visits
More information on the trial can be found on the Novo Nordisk website.
To find out more about this research study, please contact:
loth.sdcrn@nhs.scot
0131 537 3804















