US2012282248A1PendingUtilityA1
Prevention and treatment of cerebral amyloid angiopathy
Est. expiryApr 18, 2027(~0.7 yrs left)· nominal 20-yr term from priority
C07K 2317/24A61P 25/28C07K 2317/70C07K 16/18A01K 2267/0312A61K 2039/505
43
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Claims
Abstract
The invention provides improved agents and methods for treatment of cerebral amyloid angiopathy (CAA) and methods to effect prophylaxis of CAA. The methods can treat CAA concurrently with Alzheimer's disease or separately. The methods can effect prophylaxis of CAA concurrently with Alzheimer's disease or separately. The methods involve administering antibody that is specific for the N-terminus of Aβ or an agent that can induce such an antibody.
Claims
exact text as granted — not AI-modified1 - 31 . (canceled)
32 . A method of reducing vascular amyloid in a patient, comprising
administering an antibody that is specific for the N-terminus of Aβ in a treatment regime associated with efficacious vascular amyloid removal and reduced incidence of cerebral microhemorrhage.
33 . The method of claim 32 , further comprising
monitoring the patient for cerebral microhemorrhage by MRI.
34 . The method of claim 32 , further comprising
monitoring the patient for vascular amyloid removal by PET scan.
35 . The method of claim 32 , wherein the treatment regime is a chronic treatment regime.
36 . The method of claim 32 , wherein the treatment regime comprises an antibody dosage between 0.01 and 5 mg/kg body weight of the patient and administered weekly to quarterly.
37 - 42 . (canceled)
43 . The method of claim 32 , wherein the antibody is administered intravenously or subcutaneously.
44 . The method of claim 32 , wherein the antibody binds within residues 1-5 of Aβ.
45 . The method of claim 32 , wherein the antibody is a humanized, human, or chimeric antibody.
46 . The method of claim 45 , wherein the antibody is humanized 3D6 or humanized 12A11.
47 . The method of claim 46 , wherein the humanized antibody is bapineuzumab.
48 - 106 . (canceled)
107 . A method of reducing vascular amyloid in a patient, comprising
administering an antibody that is specific for the N-terminus of Aβ in a treatment regime associated with efficacious vascular amyloid removal, wherein the administration of the antibody restores normal vascular phenotype.
108 . The method of claim 107 , wherein the treatment regime is a chronic treatment regime.
109 . The method of claim 107 , wherein the treatment regime comprises an antibody dosage between 0.01 and 5 mg/kg body weight of the patient and administered weekly to quarterly.
110 - 114 . (canceled)
115 . The method of claim 109 , wherein the dosage is administered every 13 weeks.
116 . The method of claim 107 , wherein the antibody is administered intravenously or subcutaneously.
117 . The method of claim 107 , wherein the antibody binds within residues 1-5 of Aβ.
118 . The method of claim 107 , wherein the antibody is a humanized, human, or chimeric antibody.
119 . The method of claim 118 , wherein the antibody is humanized 3D6 or humanized 12A11.
120 . The method of claim 119 , wherein the humanized antibody is bapineuzumab.
121 - 135 . (canceled)Join the waitlist — get patent alerts
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