At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Trontinemab (drug), Placebo (other)
- How long the study runs
- Study runs about 27 months (dates as stated)
- About the drug or intervention
- Trontinemab — drug: Participants will receive IV trontinemab · Placebo — other: Participants will receive IV placebo
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 50 Years to 90 Years
- Who
- All
- Number of participants
- 1,060
- Started
- 2025-11-12
- Last checked
- 2026-09
Plain English Summary
What is this study?
- • Testing a new treatment for alzheimers disease
- • Phase3 - 1,060 participants
- • The purpose of this study is to assess the efficacy and safety of trontinemab in participants with early symptomatic Alzheimer's disease (AD) (mild cognitive impairment \[MCI\] to mild dementia due to AD)
Who can take part?
- • Ages 50 Years to 90 Years
- • Diagnosed with alzheimers disease
Where?
- • Bath - ReMind UK
- • Birmingham - Re:Cognition Health Birmingham
- • Edinburgh - Scottish Brain Sciences
- • Glasgow - Queen Elizabeth University Hospital Glasgow
- • +7 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The purpose of this study is to assess the efficacy and safety of trontinemab in participants with early symptomatic Alzheimer's disease (AD) (mild cognitive impairment \[MCI\] to mild dementia due to AD).
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 50 Years - 90 Years
- Who can join: All genders
What the study is looking for
- ✓Adequate visual and auditory acuity, in the investigator's judgment, sufficient to perform the neuropsychological...
- ✓Evidence of AD pathological process, as confirmed on amyloid PET scan. A CSF tau181/Aβ42 ratio may be used as an...
- ✓Probable AD dementia or MCI due to AD, also known as an Alzheimer's clinical syndrome clinical Stage 3 or Stage 4
- ✓Screening MMSE score ≥ 22 and CDR-GS of 0.5 or 1.0
- ✓Participant- and/or Informant-reported history of cognitive decline with gradual onset and progression over the last...
Who cannot take part
- ✗Any evidence of a condition other than AD that may affect cognition
- ✗History or presence of clinically significant cerebrovascular disease
- ✗History of severe, clinically significant (persistent neurologic deficit or structural brain damage) central nervous...
- ✗MRI evidence of significant cerebral abnormalities or inability to tolerate MRI procedures or safety concern to MRI
- ✗History of cancer with the following exceptions: if considered to be cured; malignancies with a negligible risk...
See the full criteria
Where Is This Study? (11 UK sites)
ReMind UK
Bath BA1 3NG, United Kingdom
Re:Cognition Health Birmingham
Birmingham B16 8QQ, United Kingdom
Scottish Brain Sciences
Edinburgh EH12 9DQ, United Kingdom
Queen Elizabeth University Hospital Glasgow
Glasgow G51 4TF, United Kingdom
St George?s Hospital
London SW17 ORE, United Kingdom
Ruth Lambley-Burke & Tilly Grocott
researchsupportservices@mpft.nhs.uk07813400821RE:Cognition Health
London W1G 8TA, United Kingdom
UCL Institute of Neurology
London WC1N 3BG, United Kingdom
Manchester Mental Health and Social Care Trust
Manchester M13 9WL, United Kingdom
Warneford Hospital
Oxford OX3 7JX, United Kingdom
Lancashire and South Cumbria NHS Foundation Trust
Preston PR2 8DW, United Kingdom
Southampton University Hospitals NHS Trust
Southampton SO16 6YD, United Kingdom
