Preventron: Trontinemab in people at risk of developing Alzheimer’s disease

Last updated 10 September 2026

Status

Open
Phase 3

Contact

The Clinical Trial Finder is for information only. To join a clinical trial you must meet the eligibility criteria set by the study and the research team will discuss this with you.

Full title
A phase III, multicenter, randomized, double-blind, placebo-controlled, parallel-group efficacy and safety study of trontinemab in cognitively unimpaired individuals at risk for progression to symptomatic Alzheimer’s disease.

Trial description

What is the aim of the study? 

The main aim of the PrevenTRON study is to find out if a new medicine called trontinemab can help stop or slow down the development of Alzheimer’s disease before it causes memory and thinking problems.

Here is what the study is testing: 

  • Helping before symptoms start: The study focuses on adults who currently have no problems with their memory or thinking, but who have changes in their brain or blood that may be linked to Alzheimer's disease. For example, they may have a build-up of a protein called amyloid, which can increase the chance of developing Alzheimer's disease in the future. 
  • Testing a new way to reach the brain: Trontinemab is designed to find amyloid in the brain and help remove it. Getting medicines into the brain can be difficult because the brain has a protective barrier that blocks many medicines. Trontinemab uses a special method called 'Brainshuttle' to help the medicine cross this barrier and reach the brain.
  • Comparing treatments: Some people in the study will get trontinemab, while others will get a placebo (a treatment that looks the same but has no medicine in it). Researchers will compare the groups over several years to see if the medicine helps keep people's brains healthy for longer.

In short, the study aims to prove whether treating the root causes of Alzheimer's disease before memory loss appears an effective way to stop or slow the disease. 

What will you be asked to do during the study? 

  • Eligibility Screening (Up to 10 weeks): Complete basic health checks, blood tests, brain scans and memory questionnaires to see if you can join the study.
  • Treatment Schedule (4 to 6 years): Receive monthly intravenous (IV) infusions of either the study drug or a placebo for the first 6 months, followed by maintenance infusions once every 6 months thereafter. 
  • Safety & Memory Tracking: Complete interactive memory tests on a tablet and undergo safety brain MRI scans roughly every 6 months. 
  • Observations & Pre-Medications: Take standard pre-medications (paracetamol and a steroid) to prevent side effects before each infusion, then stay at the clinic for 1 to 2 hours of observation. 
  • Mandatory Study Partner: Bring a close friend or family member to appointments who can answer brief questionnaires about your day-to-day routine. 

Eligibility criteria

You may be able to take part if you:

  • don't have problems with memory and daily thinking
  • have an elevated pTau217 biomarker level (this is a blood test that will be checked by the research team at the point of screening)
  • have a study partner (a close friend or family member who can come to appointments who can answer brief questionnaires about your day-to-day routine)
  • have a willingness and ability to undergo brain scans and procedures.  

You cannot take part if you:

  • have an existing diagnosis of memory impairment or dementia
  • are unable to have MRI brain scans
  • take certain medications such as blood thinners or medication to treat memory loss 
  • have uncontrolled or significant medical conditions such as high blood pressure or anaemia.

If you are unsure about whether you can or can't take part in the study, but you are interested in taking part, we recommend you send an enquiry anyway and the research team will be able to confirm if you are are eligible or not.
 

Clinical trial team

Sponsor
Roche
Chief investigator
Professor Ramin Nilforooshan, Surrey & Borders Partnership NHS Trust

Age range

55-80 years old

Recruitment start

September 2026

Disease type

Alzheimer's disease
Dementia prevention

Mechanism of action

Disease modifying therapy

Trial locations

Surrey

Length of participation

4 years

Eligibility criteria

You may be able to take part if you:

  • don't have problems with memory and daily thinking
  • have an elevated pTau217 biomarker level (this is a blood test that will be checked by the research team at the point of screening)
  • have a study partner (a close friend or family member who can come to appointments who can answer brief questionnaires about your day-to-day routine)
  • have a willingness and ability to undergo brain scans and procedures.  

You cannot take part if you:

  • have an existing diagnosis of memory impairment or dementia
  • are unable to have MRI brain scans
  • take certain medications such as blood thinners or medication to treat memory loss 
  • have uncontrolled or significant medical conditions such as high blood pressure or anaemia.

If you are unsure about whether you can or can't take part in the study, but you are interested in taking part, we recommend you send an enquiry anyway and the research team will be able to confirm if you are are eligible or not.
 

Clinical trial team

Sponsor
Roche
Chief investigator
Professor Ramin Nilforooshan, Surrey & Borders Partnership NHS Trust