| Download | - View final version: Pharmacokinetics and pharmacodynamic effect of a blood-brain barrier-crossing fusion protein therapeutic for Alzheimer’s disease in rat and dog (PDF, 1.2 MiB)
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| DOI | Resolve DOI: https://doi.org/10.1007/s11095-022-03285-z |
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| Author | Search for: Lessard, Etienne1; Search for: Rennie, Kerry1; Search for: Haqqani, Arsalan1; Search for: Ling, Binbing1; Search for: Whitfield, James1; Search for: Paradis, Andrea; Search for: Araujo, Joseph; Search for: Yoganathan, Nathan; Search for: Gillard, John; Search for: Stanimirovic, Danica1; Search for: Chakravarthy, Balu1 |
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| Affiliation | - National Research Council of Canada. Human Health Therapeutics
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| Format | Text, Article |
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| Subject | Alzheimer's disease; blood-brain barrier-crossing biologics; CNS exposure; pharmacodynamics; pharmacokinetics |
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| Abstract | We have recently demonstrated the brain-delivery of an Amyloid-ß oligomer (Aßo)-binding peptide-therapeutic fused to the BBB-crossing single domain antibody FC5. The bi-functional fusion protein, FC5-mFc-ABP (KG207-M) lowered both CSF and brain Aß levels after systemic dosing in transgenic mouse and rat models of Alzheimer’s disease (AD). For development as a human therapeutic, we have humanized and further engineered the fusion protein named KG207-H. The purpose of the present study was to carry out comparative PK/PD studies of KG207-H in wild type rat and beagle dogs (middle-aged and older) to determine comparability of systemic PK and CSF exposure between rodent species and larger animals with more complex brain structure such as dogs. |
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| Publication date | 2022-06-15 |
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| Publisher | Springer Nature |
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| Licence | |
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| In | |
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| Language | English |
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| Peer reviewed | Yes |
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| Identifier | 3285 |
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| Export citation | Export as RIS |
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| Report a correction | Report a correction (opens in a new tab) |
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| Record identifier | f46400b2-446c-49ba-a6c4-94eb4f15a6c2 |
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| Record created | 2024-02-27 |
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| Record modified | 2024-02-27 |
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