US2008181902A1PendingUtilityA1
Prevention and treatment of alzheimer's disease
Est. expiryJul 7, 2020(expired)· nominal 20-yr term from priority
A61P 37/04C07K 14/4711A61P 25/00A61K 38/00A61P 25/28A61P 25/16A61K 2039/505
61
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Claims
Abstract
The present invention relates to prevention and treatment of Alzheimer's disease (AD). More specifically, the invention relates to use of a non-wild type protofibril or compound(s) with protofibril forming activity for active immunisation in the purpose of treating or preventing AD. The invention further relates to a peptide, Aβ-Arc, with high protofibril forming activity as well as several applications thereof, such as antibodies against said peptide for passive immunisation against AD.
Claims
exact text as granted — not AI-modified1 - 21 . (canceled)
22 . An antibody suitable for prevention or treatment of an α-synuclein-related disorder, wherein said antibody binds protofibrils comprising an α-synuclein peptide.
23 . The antibody according to claim 22 , wherein said antibody is monoclonal.
24 . The antibody according to claim 22 , wherein said antibody is humanized.
25 . The antibody according to claim 22 , wherein said antibody binds protofibrils comprising an α-synuclein peptide comprising an Ala53Thr and/or Ala30Pro mutation.
26 . A method of preventing or treating an α-synuclein-related disorder, comprising the step of administering, to a patient having or suspected of having an α-synuclein-related disorder, the antibody according to claim 22 .
27 . The method according to claim 26 , wherein said alpha-synuclein-related disorder is selected from a group of disorders comprised of Parkinson's disease, dementia with Lewy Bodies, Lewy neuritis, Alzheimer's disease or Lewy Body Pathology.
28 . The method of producing the antibody according to claim 22 , comprising the steps of: immunizing a non-human animal with a protofibril comprising an α-synuclein peptide, such that antibodies against said protofibril are generated; and extracting said antibodies from said non-human animal.
29 . The method according to claim 28 , wherein said protofibril further comprises an Ala53Thr and/or Ala30Pro mutation.
30 . The method according to claim 28 , wherein said antibody is monoclonal.
31 . The method according to claim 28 , wherein said antibody is humanized.Join the waitlist — get patent alerts
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