Recruiting
Phase 3

Trontinemab

Sponsor:

Hoffmann-La Roche

Code:

NCT07717411

Conditions

Alzheimer's Disease

Eligibility Criteria

Sex: All

Age: 55 - 70+

Healthy Volunteers: Not accepted

Interventions

Trontinemab

Placebo

Study Details

Brief summary:

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.

Conditions

Alzheimer's Disease

Study ID

NCT07717411

Start date

Nov 30, 2026

Status verified date

Oct, 2026

Completion date

Sep 3, 2032

Anticipated

Primary completion date

Sep 3, 2032

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 55 - 70+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

1600 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Trontinemab

Participants will receive intravenous (IV) trontinemab.

placebo comparator: Placebo

Participants will receive IV placebo.

Interventions

Trontinemab

Participants will receive IV trontinemab.

Placebo

Participants will receive IV placebo.

Primary outcome measure

  • Time to Progression, defined as confirmed Clinical Dementia Rating - Global Score (CDR-GS) > 0 [ Time Frame: Baseline up to approximately 6 years ]

Central Contacts and Locations

Central contacts

Reference Study ID Number: WN46072 https://forpatients.roche.com

1-888-662-6728global-roche-genentech-trials@gene.com

Locations

Irvine Center for Clinical Research

Recruiting

Irvine, California, United States, 92614

Healthy Brain Clinic

Recruiting

Long Beach, California, United States, 90804

Oakland Clinical

Recruiting

Oakland, California, United States, 94609

Syrentis Clinical Research

Recruiting

Santa Ana, California, United States, 92705

K2 Medical Research, LLC

Recruiting

Maitland, Florida, United States, 32751

Renstar Medical Research

Recruiting

Ocala, Florida, United States, 34470

Charter Research - Winter Park/Orlando

Recruiting

Orlando, Florida, United States, 32803

Conquest Research - Lake Nona

Recruiting

Orlando, Florida, United States, 32832

Charter Research - Lady Lake/The Villages

Recruiting

The Villages, Florida, United States, 32162

Conquest Research, LLC

Recruiting

Winter Park, Florida, United States, 32789

Basil Clinical

Recruiting

Laurelton, New York, United States, 11413-2016

Sana Research, LLC

Recruiting

Arlington, Virginia, United States, 22205

Kelowna Health and Memory Centre Ltd.

Recruiting

Kelowna, British Columbia, Canada, V1Y 5A8

Toronto Memory Program

Recruiting

Toronto, Ontario, Canada, M3B 2S7

More Information

Sponsor

Hoffmann-La Roche

Last update posted

Oct 13, 2026

Last verified

Oct, 2026

Keywords

  • Alzheimer's
  • Alzheimer's Disease
  • pre-clinical

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-26. This information was provided to ClinicalTrials.gov by Hoffmann-La Roche on 2026-10-13. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.