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
- Remternetug (SC) (drug), Matching Placebo (Remternetug) (drug)
- How long the study runs
- Study runs about 117 months (dates as stated)
- About the drug or intervention
- Remternetug (SC) — drug: Administered subcutaneously every 12 weeks · Matching Placebo (Remternetug) — drug: Administered as subcutaneous injection of placebo every 12 weeks
- Patient visit burden
- Not specified by the sponsor
In plain English
This study, run by Washington University School of Medicine, is looking at possible treatments that may change the course of Alzheimer's disease in people who carry, or may carry, a genetic mutation that causes an inherited, early-onset form of the condition. It focuses on people who have not yet shown cognitive symptoms. Details of what the treatment involves are not stated — ask the trial team.
Who can take part
- You are at least 18 years old and can give written informed consent (with a study partner)
- You carry a mutation in the APP, PSEN1 or PSEN2 gene linked to inherited Alzheimer's, or you do not know your status but the mutation runs in your family
- You are estimated to be 11 to 25 years before the age at which cognitive symptoms would be expected to start
- Your thinking and memory are currently normal (a score called CDR-SB of 0)
- You can speak a language the study tests are available in, and can see and hear well enough to do the tests
- You have a study partner who knows you well and can answer questions about your memory and daily abilities
- Any regular medicines you take for other health problems have been at a stable dose for at least 30 days before the baseline visit
- You agree not to donate blood during the study and for a period after the final dose
- If you could become pregnant, you must not be pregnant, must avoid pregnancy and breastfeeding until 20 weeks after the last dose, and use highly effective contraception if needed
Who may not be able to
- Significant brain (other than Alzheimer's) or mental health conditions that could affect memory or your ability to take part, such as epilepsy, schizophrenia, bipolar disorder or major depression
- High risk of suicide, or thoughts of suicide or an attempt within the last 12 months
- History of stroke, mini-stroke (TIA) in the last 12 months, or major stroke risk factors
- Alcohol or drug misuse within the past year
- Brain scan findings such as certain bleeds, bruising or aneurysms, or other significant abnormalities
- Certain implanted metal devices (such as some pacemakers or heart valves) that prevent MRI scans
- Serious heart problems such as uncontrolled high blood pressure, past heart attack, heart failure or atrial fibrillation
- Significant liver or kidney problems
- HIV, recent hepatitis B, untreated hepatitis C, or certain nervous system infections such as syphilis or Lyme disease
- Severe allergies or past serious skin reactions, or sensitivity to the PET scan substances used
- Use of immunosuppressive medicines (such as steroid tablets) in the last 90 days, or cancer chemotherapy in the last 3 years
- Significant thyroid problems or vitamin B12 deficiency
- Unstable or poorly controlled diabetes (you may be retested after 3 months)
- Severe obesity with major other health problems, or that would prevent MRI scanning
- Current use of blood-thinning medicines (anticoagulants), though low-dose daily aspirin is allowed
- Having had a monoclonal antibody treatment targeting amyloid beta within the past 6 months or 5 half-lives, whichever is longer
- Taking part in another research study of an experimental drug within the past 3 months or 5 half-lives, whichever is longer
- Poor vein access for blood tests
- Abnormal blood test results that matter clinically
- A cancer history with a high risk of returning, in the researcher's view
- Any other health problem that could affect the study results or put you at extra risk
- Having taken part in another study in the last month without approval
- Having the 'Dutch' APP E693Q mutation
- Being unable to complete the baseline visit tests with suitable scores
What taking part involves
- • The specific treatments being tested are not stated — ask the trial team
- • The study includes tests such as MRI and PET scans, blood tests and memory and thinking assessments, based on the criteria above
Time commitment: Frequency of visits, how long the study lasts, and dosing details are not stated — ask the trial team.
Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 280
- Started
- 2024-11-22
- Last checked
- 2026-07
Plain English Summary
What is this study?
- • Testing a new treatment for alzheimers disease
- • Phase2/Phase3 - 280 participants
- • The purpose is to evaluate the biomarker effect, safety, and tolerability of investigational study drugs in participants who are known to have an Alzheimer's disease (AD)-causing mutation
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with alzheimers disease
Where?
- • London - The National Hospital for Neurology and Neurosurgery
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The purpose is to evaluate the biomarker effect, safety, and tolerability of investigational study drugs in participants who are known to have an Alzheimer's disease (AD)-causing mutation. Stage 1 will determine if treatment with the study drug prevents or slows the rate of amyloid beta (Aβ) pathological disease accumulation demonstrated by Aβ positron emission tomography (PET) imaging. Stage 2 will evaluate the effect of early Aβ plaque reduction/prevention on disease progression by assessing downstream non-Aβ biomarkers of AD (e.g., CSF total tau, p-tau, NfL) compared to an external control group from the DIAN-OBS natural history study and the DIAN-TU-001 placebo-treated participants.
More detail
This study will recruit participants from the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS), a multicenter international study supported by the National Institutes of Health (Grant Number U01-AG032438; RJ Bateman), Dominantly Inherited Alzheimer Network Trials Unit (DIAN-TU) sites, DIAN-TU partner sites, DIAN Expanded Registry (DIAN-EXR), and families identified by the sites. As part of the DIAN-TU-002 protocol, participants undergo longitudinal assessments that include clinical assessment, cognitive testing, magnetic resonance imaging (MRI) and amyloid imaging, and analysis of cerebrospinal fluid (CSF). Participants in DIAN are recruited from families that have at least one member who has been identified as having a mutation linked to dominantly inherited Alzheimer's disease (DIAD). The mutations in presenilin 1 (PSEN1), presenilin 2 (PSEN2) and amyloid precursor protein (APP) genes that are associated with DIAD have very high penetrance (near 100%). This study will enroll individuals who are either known to have a known disease-causing mutation, or who are at risk for such a mutation (the child or sibling of a proband with a known mutation) and unaware of their genetic status. Because the age at onset of cognitive changes is relatively consistent within each family and for each mutation, an age at onset is determined for each affected parent or mutation as part of the DIAN-OBS study protocol. This study will enroll participants who are asymptomatic and are within a specific window of time of expected age at onset for their family and/or mutation. The ability to identify individuals destined to develop Alzheimer's disease (AD) with a high degree of confidence provides a unique opportunity to assess the efficacy of therapies at asymptomatic and very early stages of dementia. Families with known disease-causing mutations are extremely rare and are geographically dispersed throughout the world. These constraints necessitate a specialized study design. Participants in this study will not yet have developed any symptoms of AD; they will be "asymptomatic" carriers of mutations that cause DIAD and would be expected to perform normally on standard cognitive and functional testing. Further, most mutation carriers will have levels of AD-associated amyloid beta (Aβ) and non-Aβ biomarkers that are the same as non-carriers. Imaging and fluid biomarkers will be used to demonstrate that the treatment compounds have engaged their therapeutic targets. A set of cognitive measures designed to assess the very earliest and most subtle cognitive changes will be collected. However, the goal of this study is to address whether decreasing plaque prone Aβ peptides in the absence of measurable or mild elevations of Aβ plaques in participants with minimal to no amyloid plaque at baseline can lead to the subsequent prevention of non-Aβ biomarkers of disease progression. Additionally, because many at-risk individuals decide not to know whether they have the disease-associated mutation, some of the at-risk individuals enrolled in this study will not have the disease-causing mutations; they will be "mutation-negative." It is important to enroll these participants to avoid coercion (e.g., potential participants may feel pressured into genetic testing to learn their genetic status to be eligible for the trial). These mutation-negative individuals will be assigned to the placebo group and data will be used to determine normal ranges of outcome. Participants and site study staff will remain blinded as to these individuals' active or placebo group assignment and mutation status. Thus, the study will be blinded for placebo and for mutation status, except for mutation carriers who are aware of their genetic status. There may be exceptional circumstances as required by local regulation or health authorities where enrollment may be restricted to mutation carriers only, but such mandates will be thoroughly documented and agreed upon by the governing regulatory agency and the study sponsor. This study is an adaptive-platform-based study. Several different therapies (each referred to as a study drug arm) may be tested in order to increase the likelihood that an effective treatment will be discovered. The compounds are selected for this trial based on mechanism of action and available data on efficacy and safety profile. In the case of multiple study arms, the study design includes a pooled placebo group (referred to as the mutation positive placebos) shared by all study drug arms. Mutation carriers will be assigned to a study drug arm and subsequently randomized within that arm in an overall 1:1 ratio to active drug: placebo. Mutation-negative participants will all receive placebo treatment. Participants and study staff will not be blinded as to which study drug arm each participant has been assigned; they will be blinded to whether participants have been randomized to receive active drug or placebo. The study has 2 treatment periods: Stage 1 is a blinded placebo-controlled period that will continue until the last randomized participant completes 4 years of treatment (i.e., a common close design), and Stage 2 is an open-label period of 4 years (with a planned 2-year interim efficacy analysis) in which all mutation carriers will receive active drug. At the start of Stage 2, participants who were randomized to placebo in Stage 1 will follow the same dose titration schedule and MRI safety schedule used in Stage 1. Participants who were randomized to active drug in Stage 1 will follow a mock dose titration and will have the same MRI safety schedule used during the initial drug titration as Stage 1 but will remain on the dose that they were on at the end of Stage 1. This will protect the blind to the original treatment assignment from Stage 1. Participants, investigators, and the sponsor's clinical team will remain blinded throughout the study to the Stage 1 treatment assignment. Stage 1 of the study is designed to test whether the study drug can slow, prevent, or reverse progression of Aβ pathology associated with AD and Stage 2 is designed to assess the study drug's effect on non-amyloid biomarkers of AD that may lead to future slowing or prevention of clinical symptoms of dementia. Biomarker, cognitive, and/or clinical endpoints will be specified for each study drug arm. Biomarker data will be analyzed for pre-specified endpoints consistent with the drug's mechanism of action and other AD biomarker outcomes. The clinical and cognitive assessments are designed to assess subtle cognitive changes that may be detectable before the onset of dementia as well as cognitive and clinical decline in symptomatic groups. Roche announced a decision to discontinue most of the company's global trials of gantenerumab. The DIAN-TU has paused the DIAN-TU-002 Primary Prevention Trial related to gantenerumab while considering other potential options for this platform trial. The DIAN-TU has re-launched the DIAN-TU-002 Primary Prevention Trial with remternetug in collaboration with Eli Lilly and Company as part of this Master Protocol. The remternetug arm is posted under NCT06647498.
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: 18 Years and over
- Who can join: All genders
Biomarkers mentioned
Treatment history
Treatments you must have had:
- ✓ a negative serum pregnancy test at screening (V1)
- ✓ study partner input for scale completion, and who signs the necessary ICF, if applicable
Treatments you must NOT have had:
- ✗ approval
What the study is looking for
- ✓Participant is at least 18 years old.
- ✓People of childbearing potential
- ✓Must have a negative serum pregnancy test at screening (V1)
- ✓Must agree not to try to become pregnant from the time of signed ICF until twenty (20) weeks after the last dose of...
- ✓Must agree not to breastfeed from the time of signed ICF until twenty (20) weeks after the last dose of any the study treatment.
Who cannot take part
- ✗Alcohol or substance use sufficient to meet DSM-V criteria currently or within the past year.
- ✗liver or kidney abnormalities that in the opinion of the investigator would interfere with participation in or...
- ✗Morbid obesity with significant other health conditions or that would preclude MRI imaging.
- ✗Current use of anticoagulants (e.g., warfarin, dabigatran, rivaroxaban, or apixaban). Daily use of low dose (\< 325...
- ✗Have been exposed to a monoclonal antibody targeting Aβ peptide within the past 6 months or 5 half-lives from...
See the full criteria
Where Is This Study? (1 UK site)
The National Hospital for Neurology and Neurosurgery
London WC1B 3BG, United Kingdom
How to Get in Touch
Jamie Bartzel
Sponsor contactCONTACT
Ellen Ziegemeier
Sponsor contactCONTACT
