ADDIA blood biomarkers
Validate the performance of ADDIA' blood biomarkers for diagnosis of Alzheimer's disease. ADDIA clinical study is a multi-centre, non-interventional, prospective, proof-of-performance study with only one visit.
400 patients with Alzheimer's disease (AD) (200 patients with mild AD, 200 patients with moderate-to-severe AD), 200 patients with non-Alzheimer's neurodegenerative diseases (NAD), and 200 controls (healthy as compared to their age)
800
blood draw, mild discomfort, in clinic visits
phlebotomist, equipped lab (e.g., centrifuge), a way to measure the peptide (e.g., mass spectrometer, protein assay kit, ELISA, western blot, or qPCR)
Amoneta Diagnostics SAS; European Commission; Firalis SA; University Hospital, Strasbourg; Centre Hospitalier Universitaire Vaudois; IRCCS Centro San Giovanni di Dio Fatebenefratelli; Hôpitaux Civils de Colmar; Istanbul University; Assistance Publique - Hôpitaux de Paris ;University Hospital, Lille; University Hospital, Geneva; Cliniques universitaires Saint-Luc- Université Catholique de Louvain; Erasme University Hospital; University Hospital, Montpellier; Centre Hospitalier Universitaire de Besancon; Centre Hospitalier Universitaire de Nice
-
“ADDIA Proof-of-Performance Clinical Study (ADDIA).” ClinicalTrials.gov. Accessed July 28, 2018. https://clinicaltrials.gov/ct2/show/NCT03030586?term=biomarker&recrs=abdf&cond=Alzheimer+Disease&draw=3&rank=30
- “Diagnosis of Alzheimer's Disease in a single drop of blood: "ADDIA ".” https://www.addia-project-h2020.eu/