Aevita Medical

Dementia and Alzheimer’s Disease Treatment

TB006 Expanded Access for Dementia and Alzheimer’s Disease

TB006 is an investigational monoclonal antibody being studied for Alzheimer’s disease and related dementias. Through Expanded Access, eligible patients who cannot participate in a clinical trial and who do not have satisfactory alternative treatment options may be able to receive TB006 under physician supervision. Our role is to evaluate candidacy, review risks and benefits, coordinate required steps, and provide treatment oversight when appropriate.

Who This May Be For

This program may be appropriate for adults with symptomatic Alzheimer’s disease or related dementias who have significant unmet needs. Based on current program materials, candidates are generally 55 or older, have an estimated or actual MMSE score of 24 or less, and are unable to enroll in a clinical trial or have exhausted, not tolerated, or are not candidates for available treatment options. Final eligibility depends on physician review, current program requirements, and any required approvals.

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Benefits of Dementia and Alzheimer’s Disease Treatment

The TB006 Expanded Access Program is designed for families seeking a more personalized, sophisticated approach to dementia care when traditional options may feel limited. While outcomes cannot be guaranteed, this investigational pathway offers access to a promising therapy within a closely supervised medical environment. Patients benefit from individualized physician oversight, attentive monitoring, and a high-touch care experience that prioritizes clarity, comfort, and thoughtful support at every step. For many, the greatest benefit is not only access to innovation, but the reassurance of navigating that process with dedicated medical guidance and exceptional continuity of care.

What to Expect
If a patient appears to be a potential fit, we begin with a detailed consultation and record review. If appropriate, we then discuss consent, program requirements, baseline evaluation, infusion planning, monitoring, and follow-up. Current program materials describe TB006 as a monthly IV infusion, typically every 28 days, administered under medical supervision.
Potential Risks and Side Effects
Because TB006 is investigational, both known and unknown risks remain possible. Reported side effects in current materials include infusion reactions, headache, upset stomach, and back pain. A full discussion of potential risks is part of the consultation process.
Costs and Planning
Expanded Access treatment may involve medication costs, physician fees, infusion-related expenses, and laboratory or monitoring costs. Specific pricing and logistics are reviewed individually before treatment is started.
How TB006 Is Being Studied
TB006 is designed to target Galectin-3, a protein being studied for its role in neuroinflammation and toxic protein aggregation. Early company-reported clinical data have suggested encouraging signals, but TB006 remains investigational and has not been established as safe or effective for routine clinical use.
Frequently Asked Questions
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What is Expanded Access?
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