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A Study of Trontinemab in Cognitively Unimpaired Individuals at Risk for Progression to Symptomatic Alzheimer's Disease (PrevenTRON)

8 septembre 2026 mis à jour par: Hoffmann-La Roche

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

This study will evaluate the efficacy and safety of trontinemab in participants with biomarker evidence of Alzheimer's Disease (AD) pathology but with no cognitive or functional impairment, who are at risk for progression to mild cognitive impairment (MCI) due to AD or dementia due to AD.

Aperçu de l'étude

Statut

Recrutement

Les conditions

Type d'étude

Interventionnel

Inscription (Estimé)

1600

Phase

  • Phase 3

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Ontario
      • Toronto, Ontario, Canada, M3B 2S7
        • Recrutement
        • Toronto Memory Program
      • Beijing, Chine, 100053
        • Recrutement
        • Xuanwu Hospital, Capital Medical University
      • Chertsey, Royaume-Uni, KT16 9AU
        • Recrutement
        • Surrey and Borders NHS Foundation Trust
    • California
      • Irvine, California, États-Unis, 92614
        • Recrutement
        • Irvine Center for Clinical Research
      • Santa Ana, California, États-Unis, 92705
        • Recrutement
        • Syrentis Clinical Research
    • Florida
      • Maitland, Florida, États-Unis, 32751
        • Recrutement
        • K2 Medical Research, LLC
    • New York
      • Laurelton, New York, États-Unis, 11413-2016
        • Recrutement
        • Basil Clinical

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Body weight of 150 kg or less
  • Willingness and ability to complete all aspects of the study for the duration of the study
  • Adequate visual and auditory acuity, in the investigator's judgment, sufficient to perform the neuropsychological testing (eyewear and hearing aids are permitted)
  • Cognitively and functionally unimpaired as defined by the protocol
  • Availability of a study partner as defined by the protocol
  • A plasma pTau217 level consistent with a high likelihood of future clinical progression

Exclusion Criteria:

  • Any evidence of a condition other than AD that may affect cognition, including, but not limited to, frontotemporal dementia, dementia with Lewy bodies, vascular dementia, Parkinson disease, corticobasal syndrome, Creutzfeldt-Jakob disease, progressive supranuclear palsy, frontotemporal lobar degeneration (other than frontotemporal dementia), Huntington disease, normal pressure hydrocephalus, seizure disorder, delirium, or hypoxia
  • Mild cognitive impairment (MCI; may be referred to as prodromal AD), or any form of dementia
  • History or presence of clinically significant cerebrovascular disease
  • History of severe, clinically significant (persistent neurologic deficit or structural brain damage) central nervous system (CNS) trauma
  • History or presence of clinically significant intracranial mass
  • History of schizophrenia, schizoaffective disorder, major depression, or bipolar disorder
  • History or presence of any stroke with clinical symptoms within the past 12 months, or documented history within the last 12 months of an acute event that is consistent, in the opinion of the PI, with a transient ischemic attack
  • At risk for suicide in the opinion of the investigator
  • Substance abuse disorder within 12 months prior to screening (nicotine use is allowed)
  • Any other medical conditions (e.g., cardiovascular, hepatic, renal disease) which are not stable and adequately controlled or which in the opinion of the investigator could affect the participant's safety in the study or interfere with the study assessments
  • Uncontrolled hypertension
  • Impaired hepatic function
  • History or presence of any clinically significant hematological diseases
  • Diagnosis of a wet age-related macular degeneration (AMD)
  • Abnormal thyroid function
  • Abnormally low serum levels of folic acid or vitamin B12 deficiency that are judged to be clinically significant and/or may impact cognition as per the investigator's judgment
  • Current HIV, hepatitis B, or hepatitis C infection that has not been adequately treated in the opinion of the investigator
  • History of malignancy
  • Any previous administration of active immunotherapy (vaccine) that is being evaluated to prevent or postpone cognitive decline
  • Any previous or current use of passive immunotherapy (immunoglobulin) or other long-acting biologic agent that is approved or under evaluation or has been evaluated to prevent or postpone cognitive decline
  • Any other investigational treatment within 5 half-lives or 4 months prior to screening, whichever is longer
  • Intravenous (IV) or subcutaneous immunoglobulin therapy within 5 half-lives or 4 months prior to baseline whichever is longer
  • Anticoagulation medications at screening and there should be no plans to initiate any prior to or after randomization
  • Any treatment with cholinesterase inhibitors
  • Antipsychotic or neuroleptic medications within 3 months of screening, except as brief treatment for a non-psychiatric indication
  • Individuals with chronic use of opiates or opioids, benzodiazepines, barbiturates, or hypnotics, antidepressants or medication to treat anxiety should be on a stable dose for at least 8 weeks before baseline
  • Currently enrolled in an interventional study including those requiring investigational medicinal product (IMP) or involving any type of medical research that may interfere with study cognitive assessments
  • Residence in a skilled nursing facility such as a convalescent home or long-term care facility

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Trontinémab
Les participants recevront un trontemab intraveineux (IV).
Les participants recevront un trontinemab IV.
Comparateur placebo: Placebo
Les participants recevront un placebo IV.
Participants will receive IV placebo.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Time to Progression, defined as confirmed Clinical Dementia Rating - Global Score (CDR-GS) > 0
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years

Mesures de résultats secondaires

Mesure des résultats
Délai
Change from Baseline through Week 216 in Clinical Dementia Rating, Sum of Boxes (CDR-SB)
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Free and Cued Selective Reminding Test (FCSRT) total recall score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Digit Symbol Substitution Test (DSST) coding score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Cognitive Function Instrument (CFI) study partner, total score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Category fluency total score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Mini-Mental State Examination (MMSE) total score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Wechsler Memory Scale, Logical Memory II Delayed Paragraph Recall (WMS LM II [DR]) score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Amsterdam Instrumental Activities of Daily Living Questionnaire-Short Version (A-IADL-Q-SV) study partner, total score
Délai: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Trail Making Test (TMT)
Délai: Baseline through Week 216
Baseline through Week 216
Time to progression to adjudicated mild cognitive impairment (MCI) diagnosis
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Incidence of adverse events
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Frequency of amyloid-related imaging abnormalities-edema/effusion (ARIA-E) and amyloid-related imaging abnormalities-hemosiderin deposition (ARIA-H) magnetic resonance imaging (MRI) findings
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Severity of ARIA-E and ARIA-H MRI findings
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Frequency of infusion-related reactions (IRRs)
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Severity of IRRs
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Incidence of anti-drug antibodies (ADAs) to trontinemab
Délai: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Change from baseline through Week 216 in brain amyloid load, as measured by amyloid positron emission tomography (PET) scan
Délai: Baseline through Week 216
Baseline through Week 216
Change from baseline through Week 216 in blood biomarker phosphorylated tau 217 (pTau217)
Délai: Baseline through Week 216
Baseline through Week 216
Change from baseline through Week 216 in blood biomarker glial fibrillar acidic protein (GFAP)
Délai: Baseline through Week 216
Baseline through Week 216

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Directeur d'études: Clinical Trials, Hoffmann-La Roche

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

30 novembre 2026

Achèvement primaire (Estimé)

3 septembre 2032

Achèvement de l'étude (Estimé)

3 septembre 2032

Dates d'inscription aux études

Première soumission

17 juillet 2026

Première soumission répondant aux critères de contrôle qualité

17 juillet 2026

Première publication (Réel)

21 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

10 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

8 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

For eligible studies, qualified researchers may request access to individual patient level clinical data. See Roche's commitment to transparency of clinical study information here: https://go.roche.com/data_sharing

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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