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R44NIH · NATIONAL INSTITUTE ON AGINGNIH

Single domain antibody development for improving vascular dysfunction in Alzheimer’s disease

Hussain, Sazid (Contact)·AIVOCODE, LLP, CA·2025–2027·ACTIVE
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INSTITUTION

AIVOCODE, LLP, CA

PRINCIPAL INVESTIGATOR

Hussain, Sazid (Contact)

FUNDING

$1.2M

YEAR

2025

MOONBASE SCORE

Still being scored

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Abstract

Alzheimer's disease (AD) is the most common form of neurodegenerative disorder associated with aging. One of the hallmarks of this disorder is the progressive loss of neuronal cells, which ultimately becomes fatal. Several lines of investigations characterized by the loss of mural cells (pericytes) and compromised blood-brain-barrier, in pathogenesis of AD. Academic collaborators and founders of AivoCode Inc., the applicant company, have employed unbiased screening with in vivo phage display to probe specific vascular signature present in the brains of transgenic AD mice. This new approach to AD studies has generated a new and understudied therapeutic target, connective tissue growth factor (CTGF). CTGF binds extracellular matrices and cell surfaces including brain vasculature in AD mice and can stimulate endothelial cell migration and angiogenesis. Our preliminary data suggests that CTGF plays a role in causing abnormalities in AD brain vessels and can potentially be a new therapeutic target for AD drug development. In this Phase II application, we propose to test single domain antibodies against CTGF to neutralize CTGF activity in mouse models of AD to improve vascular dysfunction and test if it leads to slower disease progression. The results of this study will provide a lead single domain antibody as a drug candidate for further development for AD.

R44NATIONAL INSTITUTE ON AGINGSpecial Emphasis Panel[ZAG1 ZIJ-2 (M2)]modelsdomainbraincandidatefurthervesselsleadsphasebecomespresentabnormalitiesfactorultimatelydiseaselinesscreeningprogressivephageaivocode

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