- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07717411
A Study of Trontinemab in Cognitively Unimpaired Individuals at Risk for Progression to Symptomatic Alzheimer's Disease (PrevenTRON)
8. September 2026 aktualisiert von: 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.
Studienübersicht
Status
Rekrutierung
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Geschätzt)
1600
Phase
- Phase 3
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Reference Study ID Number: WN46072 https://forpatients.roche.com
- Telefonnummer: 1-888-662-6728
- E-Mail: global-roche-genentech-trials@gene.com
Studienorte
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Beijing, China, 100053
- Rekrutierung
- Xuanwu Hospital, Capital Medical University
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Ontario
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Toronto, Ontario, Kanada, M3B 2S7
- Rekrutierung
- Toronto Memory Program
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California
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Irvine, California, Vereinigte Staaten, 92614
- Rekrutierung
- Irvine Center for Clinical Research
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Santa Ana, California, Vereinigte Staaten, 92705
- Rekrutierung
- Syrentis Clinical Research
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Florida
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Maitland, Florida, Vereinigte Staaten, 32751
- Rekrutierung
- K2 Medical Research, LLC
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New York
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Laurelton, New York, Vereinigte Staaten, 11413-2016
- Rekrutierung
- Basil Clinical
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Chertsey, Vereinigtes Königreich, KT16 9AU
- Rekrutierung
- Surrey and Borders NHS Foundation Trust
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
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
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Trontinemab
Die Teilnehmer erhalten intravenöses (IV) Trontinemab.
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Die Teilnehmer erhalten IV Trontinemab.
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Placebo-Komparator: Placebo
Die Teilnehmer erhalten IV Placebo.
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Participants will receive IV placebo.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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Time to Progression, defined as confirmed Clinical Dementia Rating - Global Score (CDR-GS) > 0
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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Change from Baseline through Week 216 in Clinical Dementia Rating, Sum of Boxes (CDR-SB)
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Free and Cued Selective Reminding Test (FCSRT) total recall score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Digit Symbol Substitution Test (DSST) coding score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Cognitive Function Instrument (CFI) study partner, total score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Category fluency total score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Mini-Mental State Examination (MMSE) total score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Wechsler Memory Scale, Logical Memory II Delayed Paragraph Recall (WMS LM II [DR]) score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Amsterdam Instrumental Activities of Daily Living Questionnaire-Short Version (A-IADL-Q-SV) study partner, total score
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from Baseline through Week 216 in Trail Making Test (TMT)
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Time to progression to adjudicated mild cognitive impairment (MCI) diagnosis
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Incidence of adverse events
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Frequency of amyloid-related imaging abnormalities-edema/effusion (ARIA-E) and amyloid-related imaging abnormalities-hemosiderin deposition (ARIA-H) magnetic resonance imaging (MRI) findings
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Severity of ARIA-E and ARIA-H MRI findings
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Frequency of infusion-related reactions (IRRs)
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Severity of IRRs
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Incidence of anti-drug antibodies (ADAs) to trontinemab
Zeitfenster: Baseline up to approximately 6 years
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Baseline up to approximately 6 years
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Change from baseline through Week 216 in brain amyloid load, as measured by amyloid positron emission tomography (PET) scan
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from baseline through Week 216 in blood biomarker phosphorylated tau 217 (pTau217)
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Change from baseline through Week 216 in blood biomarker glial fibrillar acidic protein (GFAP)
Zeitfenster: Baseline through Week 216
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Baseline through Week 216
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Studienleiter: Clinical Trials, Hoffmann-La Roche
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
30. November 2026
Primärer Abschluss (Geschätzt)
3. September 2032
Studienabschluss (Geschätzt)
3. September 2032
Studienanmeldedaten
Zuerst eingereicht
17. Juli 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
17. Juli 2026
Zuerst gepostet (Tatsächlich)
21. Juli 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
10. September 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
8. September 2026
Zuletzt verifiziert
1. September 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- WN46072
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
JA
Beschreibung des IPD-Plans
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
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Ja
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .