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

8 de setembro de 2026 atualizado por: 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.

Visão geral do estudo

Status

Recrutamento

Condições

Tipo de estudo

Intervencional

Inscrição (Estimado)

1600

Estágio

  • Fase 3

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Ontario
      • Toronto, Ontario, Canadá, M3B 2S7
        • Recrutamento
        • Toronto Memory Program
      • Beijing, China, 100053
        • Recrutamento
        • Xuanwu Hospital, Capital Medical University
    • California
      • Irvine, California, Estados Unidos, 92614
        • Recrutamento
        • Irvine Center for Clinical Research
      • Santa Ana, California, Estados Unidos, 92705
        • Recrutamento
        • Syrentis Clinical Research
    • Florida
      • Maitland, Florida, Estados Unidos, 32751
        • Recrutamento
        • K2 Medical Research, LLC
    • New York
      • Laurelton, New York, Estados Unidos, 11413-2016
        • Recrutamento
        • Basil Clinical
      • Chertsey, Reino Unido, KT16 9AU
        • Recrutamento
        • Surrey and Borders NHS Foundation Trust

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Quadruplicar

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Trontinemab
Os participantes receberão Trontinemab intravenoso (iv).
Os participantes receberão IV Trontinemab.
Comparador de Placebo: Placebo
Os participantes receberão IV placebo.
Participants will receive IV placebo.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Time to Progression, defined as confirmed Clinical Dementia Rating - Global Score (CDR-GS) > 0
Prazo: Baseline up to approximately 6 years
Baseline up to approximately 6 years

Medidas de resultados secundários

Medida de resultado
Prazo
Change from Baseline through Week 216 in Clinical Dementia Rating, Sum of Boxes (CDR-SB)
Prazo: 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
Prazo: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Digit Symbol Substitution Test (DSST) coding score
Prazo: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Cognitive Function Instrument (CFI) study partner, total score
Prazo: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Category fluency total score
Prazo: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Mini-Mental State Examination (MMSE) total score
Prazo: 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
Prazo: 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
Prazo: Baseline through Week 216
Baseline through Week 216
Change from Baseline through Week 216 in Trail Making Test (TMT)
Prazo: Baseline through Week 216
Baseline through Week 216
Time to progression to adjudicated mild cognitive impairment (MCI) diagnosis
Prazo: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Incidence of adverse events
Prazo: 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
Prazo: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Severity of ARIA-E and ARIA-H MRI findings
Prazo: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Frequency of infusion-related reactions (IRRs)
Prazo: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Severity of IRRs
Prazo: Baseline up to approximately 6 years
Baseline up to approximately 6 years
Incidence of anti-drug antibodies (ADAs) to trontinemab
Prazo: 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
Prazo: Baseline through Week 216
Baseline through Week 216
Change from baseline through Week 216 in blood biomarker phosphorylated tau 217 (pTau217)
Prazo: Baseline through Week 216
Baseline through Week 216
Change from baseline through Week 216 in blood biomarker glial fibrillar acidic protein (GFAP)
Prazo: Baseline through Week 216
Baseline through Week 216

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Diretor de estudo: Clinical Trials, Hoffmann-La Roche

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

30 de novembro de 2026

Conclusão Primária (Estimado)

3 de setembro de 2032

Conclusão do estudo (Estimado)

3 de setembro de 2032

Datas de inscrição no estudo

Enviado pela primeira vez

17 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

17 de julho de 2026

Primeira postagem (Real)

21 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

10 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

8 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano 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

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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