An observational study in Alzheimer, sponsored by Firalis SA. Recruiting at 1 site in France. Open to participants aged 45 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-02.
Sponsored by Firalis SA · Observational
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Among 438 studies in Alzheimer Disease with a site in France — 80 open to participants now, 97 under way, 19 of them phase 3. Alzheimer Disease · France.
Among the 438 studies in Alzheimer Disease with a site in France, this one is the 3rd largest by planned enrollment of the 93 observational ones that give a count, is one of 15 that started in 2026, is one of 95 observational ones, reaches primary completion later than 40 of the 96 other live ones, and was the 436th registered.
3,968 studies on the registry are indexed under Alzheimer Disease; 928 are open to participants now.
Browse Alzheimer Disease studies →80 of the 438 studies in Alzheimer Disease with a site in France are open now. Recruiting first, the newest first:
Hoffmann-La Roche · Sites in France, United States, Australia
Ages 50–90
Centre Hospitalier Universitaire de Saint Etienne · Sites in France
Ages 60+ · Healthy volunteers
University Hospital, Toulouse · Sites in France
Ages 50–85
Central Hospital, Nancy, France · Sites in France
Ages 18–99
Assistance Publique - Hôpitaux de Paris · Sites in France
Ages 50–80
A study can be open while its sites in France have not opened yet or have stopped. Only those recruiting at a site in France →
Of the 643 Alzheimer Disease studies recruiting now, 284 (44%) set no upper age limit and 55 (9%) stop at 75 or younger; 34 take children under 18; 285 take healthy volunteers.
This study: 45 Years and older · all sexes · healthy volunteers too.
The full table on the hub →This tab as a report to print or save as PDF → With an account.
438 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 1 24 · Phase 2 72 · Phase 3 88 · Phase 4 7
First in 2001; this study’s year is marked. 15 started in 2026.
By drug class, each counting the studies that test any of its medicines:
This study's planned enrollment of 50,000 is above the median of 200 across 815 observational studies indexed under Alzheimer Disease.
Median enrollment 154 across the 342 interventional studies, 140 across the 93 observational. Of the 290 that completed or were terminated, 74 (26%) have results posted.
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156 of 438 have an industry lead sponsor. The 10 most frequent:
Firalis SA is the lead sponsor of 7 studies on the registry; 3 are open to participants now.
Firalis SA has 2 studies filed under Alzheimer Disease — fewer than ten, so there is no comparison to draw.
32 of the studies in Alzheimer Disease with a site in France that are under way reach primary completion within a year, 3 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT06585787Phase 3Karuna Therapeutics, Inc., a Bristol Myers Squibb companyA Study to Evaluate KarXT as a Treatment for Psychosis Associated With Alzheimer's Disease (ADEPT-4) | 2026-11-24 |
| NCT03887455Phase 3Eisai Inc.A Study to Confirm Safety and Efficacy of Lecanemab in Participants With Early Alzheimer's Disease | 2026-12-31 |
| NCT05980949Phase 3Karuna Therapeutics, Inc., a Bristol Myers Squibb companyOpen-Label Extension Study to Assess the Long-Term Safety and Tolerability of KarXT in Subjects With Psychosis Associated With Alzheimer's Disease (ADEPT-3) | 2027-09-07 |
| NCT06080659Rennes University HospitalNetwork-based biOmarker Discovery of Neurodegenerative Diseases Using Multimodal Connectivity | 2026-11 |
| NCT06402838Hoffmann-La RocheA Study to Evaluate the Safety and Biomarker Effects of RO7269162 in Participants at Risk for or at the Prodromal Stage of Alzheimer's Disease (AD) | 2026-11-19 |
Add all 32 to your calendar (.ics) → With an account.
Among the 438 studies in Alzheimer Disease with a site in France, from their registry updates:
This tab as a report to print or save as PDF → With an account.
ALZEVIT is a nationwide, decentralized, digital-first cohort study in France designed to establish a large-scale Apolipoprotein E (APOE) genotyping registry and enable precision prevention strategies for Alzheimer's disease (AD). Sponsored by Firalis SA and conducted in collaboration with French memory centers, it addresses the need for early identification of individuals at high genetic risk, particularly APOE ε4 carriers and ε4/ε4 homozygotes, in the context of emerging disease-modifying therapies most effective in preclinical or early disease stages.
Using an online recruitment platform, participants aged ≥45 years provide electronic informed consent and self-collected saliva samples via home collection kits for centralized APOE genotyping using the APO-Easy® assay, compliant with EU IVDR and US FDA requirements. Data are stored in a secure registry compliant with GDPR.
Phase A (0-18 months) will enroll 50,000 participants to determine national APOE genotype distribution, identify high-risk individuals, and evaluate feasibility of large-scale digital genetic screening, with longitudinal online follow-up including cognitive and risk factor assessments.
Phase B (12-24 months) includes detailed phenotyping of \~2,350 selected participants across all APOE genotypes, including \~750 ε4/ε4 homozygotes. Participants undergo clinical evaluation, MRI, cognitive testing, and multi-omics biomarker profiling (genomics, proteomics, metabolomics, environmental exposure), conducted at memory centers or via telemedicine.
The study classifies participants along the cognitive continuum, including cognitively normal individuals, preclinical AD, mild cognitive impairment (MCI), and mild or moderate AD, to identify genotype-specific trajectories and modifiable risk and resilience factors. ALZEVIT aims to establish a scalable national infrastructure linking genetic stratification with longitudinal biomarker and clinical data to support prevention trials, improve understanding of APOE-related heterogeneity, and advance precision medicine for Alzheimer's disease.
ALZEVIT is a nationwide, decentralized, digital-first observational cohort designed to establish a large-scale APOE genotyping registry in France and create a trial-ready infrastructure for precision prevention in Alzheimer's disease (AD). The study is sponsored by Firalis SA and conducted in collaboration with multiple French memory research centers, including the Centres Mémoire de Ressources et de Recherche (CMRR) network and Centres Hospitaliers Universitaires (CHU). The study integrates digital health tools, centralized genetic testing, and longitudinal phenotyping to address the need for early identification and stratification of individuals at risk for late-onset Alzheimer's disease.
Alzheimer's disease is a progressive neurodegenerative disorder and the leading cause of dementia worldwide. Recent advances, including disease-modifying therapies such as anti-amyloid monoclonal antibodies, have demonstrated that treatment is most effective when initiated during the earliest stages of disease before extensive neurodegeneration occurs. However, implementation remains limited by safety considerations, including amyloid-related imaging abnormalities (ARIA), substantial infrastructure requirements, and restricted access in many healthcare systems. These challenges highlight the need to identify individuals at elevated risk before symptom onset and to facilitate scalable and ethically appropriate recruitment into prevention trials.
Genetic stratification has emerged as one of the most robust approaches for identifying individuals at increased risk of Alzheimer's disease. Among known genetic factors, APOE ε4 is the strongest common genetic risk allele for late-onset Alzheimer's disease and is associated with increased amyloid deposition, tau pathology, neuroinflammation, lipid dysregulation, and earlier disease onset. APOE ε4/ε4 homozygotes represent a particularly high-risk subgroup with earlier biomarker changes and accelerated cognitive decline. Although they comprise approximately 1.5% to 2.5% of the general population, they account for a disproportionately large proportion of Alzheimer's disease cases. Conversely, APOE ε2 is associated with reduced risk, and APOE ε2/ε2 homozygosity represents a model of resilience. Emerging evidence supports classification of APOE ε4/ε4 homozygosity as a distinct genetic subtype of Alzheimer's disease characterized by specific biological trajectories and early amyloid accumulation.
The therapeutic landscape for Alzheimer's disease continues to evolve, with investigational therapies targeting multiple biological pathways, including synaptic resilience, cellular stress responses, autophagy modulation, and APOE-directed interventions. This evolving landscape reinforces the need for genetically and biologically stratified populations to support precision prevention and treatment. Consequently, well-characterized longitudinal cohorts are becoming essential infrastructure for future clinical research.
Within this context, ALZEVIT is designed as a scalable national platform enabling population-level APOE genotyping and longitudinal characterization of cognitive, clinical, and biological trajectories. Participants enroll online, provide electronic informed consent, and receive ORAcollect® Dx saliva collection kits. Samples are returned to a centralized laboratory for APOE genotyping using the APO-Easy® assay, a European Union In Vitro Diagnostic Regulation (IVDR)- and United States Food and Drug Administration (FDA)-compliant diagnostic platform with high concordance to sequencing methods.
Phase A (Months 0-18) aims to enroll 50,000 adults aged 45 years and older across France. Participants are stratified into five age groups (45-54, 55-64, 65-74, 75-84, and 85 years or older) to estimate age-specific genotype frequencies. The primary objectives are to determine the national distribution of APOE genotypes, establish a secure General Data Protection Regulation (GDPR)-compliant registry, identify individuals at highest genetic risk, particularly APOE ε4/ε4 homozygotes, and evaluate the feasibility and scalability of decentralized digital genetic screening.
Participants provide self-reported information on demographics, family history of dementia, vascular and metabolic risk factors including hypertension, diabetes mellitus, dyslipidemia, and body mass index (BMI), lifestyle factors including physical activity, diet, smoking, alcohol consumption, sleep quality, mood, hearing status, and medication use. Participants also complete validated cognitive assessments and questionnaires assessing subjective cognitive decline. Periodic remote follow-up assessments monitor cognitive changes and risk factor evolution.
The registry is intended to serve as a national infrastructure for Alzheimer's disease prevention research by supporting longitudinal follow-up, facilitating recruitment into prevention trials, and providing evidence regarding genotype-specific disease trajectories.
Phase B (Months 12-24) includes comprehensive phenotyping of approximately 2,350 participants representing all APOE genotypes, including approximately 750 APOE ε4/ε4 homozygotes. Participants undergo clinical evaluations, standardized neuropsychological testing, magnetic resonance imaging (MRI), and biomarker assessments at participating memory centers or through telemedicine.
Neuropsychological testing includes the Mini-Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), and digital cognitive batteries. Core Alzheimer's disease biomarkers, including amyloid-beta peptide 40 (Aβ40), amyloid-beta peptide 42 (Aβ42), phosphorylated tau 217 (p-tau217), phosphorylated tau 181 (p-tau181), and total tau, are measured using validated in vitro diagnostic (IVD) platforms. Additional genetic analyses are performed using extended neurodegeneration gene panels. Participants are classified as cognitively normal, having preclinical Alzheimer's disease, having Mild Cognitive Impairment due to Alzheimer's disease, or having mild to moderate Alzheimer's disease.
A major component of Phase B is integrated multi-omics and environmental exposure profiling. Saliva, whole blood, serum, plasma, and urine samples are collected and stored in a biobank certified according to International Organization for Standardization (ISO) 20387. Analyses include genomic, transcriptomic, proteomic, metabolomic, and environmental exposure analyses to identify biological pathways and biomarkers associated with disease onset and progression.
The study also evaluates modifiable risk and resilience factors, including cardiovascular and metabolic health, physical activity, sleep, dietary habits, mood, anxiety symptoms, social engagement, hearing impairment, and medication use. These variables will be examined in relation to cognitive trajectories, biomarker evolution, and clinical progression.
Comparative analyses across APOE genotypes are central to the study design. APOE ε4/ε4 homozygotes will be compared with other genotype groups to characterize differences in biomarker profiles, neuroimaging findings, and cognitive trajectories across age groups. These analyses aim to improve understanding of APOE ε4/ε4 as a distinct genetic subtype of Alzheimer's disease and to inform future population screening strategies.
Operationally, ALZEVIT will evaluate the feasibility of large-scale decentralized neurological research, including recruitment efficiency, participant adherence, sample return rates, data completeness, and the quality of remotely collected genetic and clinical data. Hybrid approaches combining digital follow-up with targeted in-person assessments will also be evaluated.
Ethical oversight includes compliance with the General Data Protection Regulation (GDPR), implementation of data minimization principles, independent data protection monitoring, and secure management of genetic information. Participants retain full informed consent rights, and study data are used only for approved research purposes.
ALZEVIT is intended to establish a national infrastructure supporting Alzheimer's disease prevention and precision medicine by integrating population-scale APOE genotyping with longitudinal cognitive, clinical, and biomarker data. The study is expected to facilitate recruitment into prevention and early intervention trials, improve understanding of genotype-specific disease trajectories, support personalized risk prediction, and contribute to strategies that reduce the future burden of Alzheimer's disease.
Phase A: ALZEVIT will enroll 50,000 French adults aged ≥45 years, stratified across five age groups. Participants will complete online risk-factor and cognitive assessments and provide a home-collected saliva sample for APOE genotyping. The study is expected to identify approximately 750 APOE ε4/ε4 homozygotes and establish a secure, GDPR-compliant national APOE registry.
Phase B: A subset of 2,350 participants representing all six APOE genotypes, including 750 ε4/ε4 homozygotes, will undergo detailed clinical, cognitive, MRI, and biomarker evaluations. The objective is to characterize genotype-specific trajectories and classify participants according to Alzheimer's disease stage, from cognitively normal to preclinical AD, MCI-AD, and mild/moderate AD.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ε2/ε2 (45-54)
ε2/ε2 (55-64)
ε2/ε2 (65-74)
ε2/ε2 (75-84)
ε2/ε2 (≥85)
ε2/ε3 (45-54)
ε2/ε3 (55-64)
ε2/ε3 (65-74)
ε2/ε3 (75-84)
ε2/ε3 (≥85)
ε2/ε4 (45-54)
ε2/ε4 (55-64)
ε2/ε4 (65-74)
ε2/ε4 (75-84)
ε2/ε4 (≥85)
ε3/ε4 (45-54)
ε3/ε4 (55-64)
ε3/ε4 (65-74)
ε3/ε4 (75-84)
ε3/ε4 (≥85)
ε3/ε3 (45-54)
ε3/ε3 (55-64)
ε3/ε3 (65-74)
ε3/ε3 (75-84)
ε3/ε3 (≥85)
ε4/ε4 (45-54)
ε4/ε4 (55-64)
ε4/ε4 (65-74)
ε4/ε4 (75-84)
ε4/ε4 (≥85)
1. APOE genotype distribution in the study population
Proportion and frequency of APOE genotypes (ε2/ε2, ε2/ε3, ε2/ε4, ε3/ε3, ε3/ε4, ε4/ε4) in adults aged ≥45 years in France, stratified by age group.
Time frame: through study completion, an average of 2 years
2. Feasibility of large-scale decentralized APOE genotyping registry
Operational performance of the digital-first model, including rates of electronic consent completion, home saliva kit return, DNA sample adequacy, and successful centralized APOE genoty
Time frame: through study completion, an average of 2 years
3. Identification of APOE ε4/ε4 homozygotes in the national cohort
Number and proportion of ε4/ε4 individuals identified across age strata and successfully enrolled in the registry.
Time frame: through study completion, an average of 2 years
4. Establishment of a secure longitudinal APOE registry
Creation of a GDPR-compliant database enabling longitudinal follow-up of participants with APOE genotype linked to minimal clinical and demographic data for future risk stratification and trial read
Time frame: through study completion, an average of 2 years
Plan to share: Yes — Results will be share with participants who are willing to have them
Start is estimated for Sep 2026; primary completion for May 2027, 8 months later.
How these figures are worked out, and which studies are left out of them.
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Firalis SA