- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07717411
A Study of Trontinemab in Cognitively Unimpaired Individuals at Risk for Progression to Symptomatic Alzheimer's Disease (PrevenTRON)
8. september 2026 oppdatert av: 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.
Studieoversikt
Status
Rekruttering
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
1600
Fase
- Fase 3
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Reference Study ID Number: WN46072 https://forpatients.roche.com
- Telefonnummer: 1-888-662-6728
- E-post: global-roche-genentech-trials@gene.com
Studiesteder
-
-
Ontario
-
Toronto, Ontario, Canada, M3B 2S7
- Rekruttering
- Toronto Memory Program
-
-
-
-
California
-
Irvine, California, Forente stater, 92614
- Rekruttering
- Irvine Center for Clinical Research
-
Santa Ana, California, Forente stater, 92705
- Rekruttering
- Syrentis Clinical Research
-
-
Florida
-
Maitland, Florida, Forente stater, 32751
- Rekruttering
- K2 Medical Research, LLC
-
-
New York
-
Laurelton, New York, Forente stater, 11413-2016
- Rekruttering
- Basil Clinical
-
-
-
-
-
Beijing, Kina, 100053
- Rekruttering
- Xuanwu Hospital, Capital Medical University
-
-
-
-
-
Chertsey, Storbritannia, KT16 9AU
- Rekruttering
- Surrey and Borders NHS Foundation Trust
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Trontinemab
Deltakerne vil motta intravenøs (iv) trontinemab.
|
Deltakerne vil motta IV Trontinemab.
|
|
Placebo komparator: Placebo
Deltakerne vil motta IV placebo.
|
Participants will receive IV placebo.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Time to Progression, defined as confirmed Clinical Dementia Rating - Global Score (CDR-GS) > 0
Tidsramme: Baseline up to approximately 6 years
|
Baseline up to approximately 6 years
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change from Baseline through Week 216 in Clinical Dementia Rating, Sum of Boxes (CDR-SB)
Tidsramme: 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
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from Baseline through Week 216 in Digit Symbol Substitution Test (DSST) coding score
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from Baseline through Week 216 in Cognitive Function Instrument (CFI) study partner, total score
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from Baseline through Week 216 in Category fluency total score
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from Baseline through Week 216 in Mini-Mental State Examination (MMSE) total score
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from Baseline through Week 216 in Trail Making Test (TMT)
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Time to progression to adjudicated mild cognitive impairment (MCI) diagnosis
Tidsramme: Baseline up to approximately 6 years
|
Baseline up to approximately 6 years
|
|
Incidence of adverse events
Tidsramme: 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
Tidsramme: Baseline up to approximately 6 years
|
Baseline up to approximately 6 years
|
|
Severity of ARIA-E and ARIA-H MRI findings
Tidsramme: Baseline up to approximately 6 years
|
Baseline up to approximately 6 years
|
|
Frequency of infusion-related reactions (IRRs)
Tidsramme: Baseline up to approximately 6 years
|
Baseline up to approximately 6 years
|
|
Severity of IRRs
Tidsramme: Baseline up to approximately 6 years
|
Baseline up to approximately 6 years
|
|
Incidence of anti-drug antibodies (ADAs) to trontinemab
Tidsramme: 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
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from baseline through Week 216 in blood biomarker phosphorylated tau 217 (pTau217)
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
|
Change from baseline through Week 216 in blood biomarker glial fibrillar acidic protein (GFAP)
Tidsramme: Baseline through Week 216
|
Baseline through Week 216
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studieleder: Clinical Trials, Hoffmann-La Roche
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
30. november 2026
Primær fullføring (Antatt)
3. september 2032
Studiet fullført (Antatt)
3. september 2032
Datoer for studieregistrering
Først innsendt
17. juli 2026
Først innsendt som oppfylte QC-kriteriene
17. juli 2026
Først lagt ut (Faktiske)
21. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
10. september 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
8. september 2026
Sist bekreftet
1. september 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- WN46072
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
JA
IPD-planbeskrivelse
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
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Ja
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .