Irvine, CANCT07717411Now EnrollingIRB Ready

Alzheimer's Disease Clinical Trial in Irvine, CA

Access cutting-edge alzheimer's disease treatment through this phase 3 clinical trial at a research site in Irvine. Study-provided care at no cost to qualified participants.

Sponsored by Hoffmann-La Roche

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Expert Care in Irvine

Access alzheimer's disease specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related alzheimer's disease treatment provided free

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Check if you qualify for this alzheimer's disease clinical trial in Irvine, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Irvine

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Irvine site if eligible
  4. 4Begin participation

About This Alzheimer's Disease Study in Irvine

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.

Sponsor: Hoffmann-La Roche

Who Can Participate

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Irvine?

Yes, this clinical trial (NCT07717411) has an active research site in Irvine, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Alzheimer's Disease Treatment Options in Irvine, CA

If you're searching for alzheimer's disease treatment options in Irvine, CA, this clinical trial (NCT07717411) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Irvine research site is actively enrolling participants for this phase 3 clinical trial. You'll receive care from experienced alzheimer's disease specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all alzheimer's disease clinical trials near you to find additional studies recruiting in your area.

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See all alzheimers disease clinical trials recruiting in Irvine — not just this study.

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Secure · Expert Care · Irvine, CA