Method for the treatment of amyloidoses
First Claim
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1. A method for the treatment of an amyloidosis disease comprising administering to a subject in need thereof an agent that inhibits the interaction between Aβ
- globulomer and P/Q type voltage-gated presynaptic calcium channel, wherein the agent is an antibody that binds to the P/Q type voltage-gated presynaptic calcium channel, wherein the amyloidosis disease is selected from the group consisting of Alzheimer'"'"'s disease and Down'"'"'s syndrome, wherein the antibody is raised against a peptide mapping near the C-terminus of the α
1A subunit of the P/Q type voltage-gated presynaptic calcium channel, and wherein the antibody is sc-16228.
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Abstract
The present invention relates to a method for the treatment of an amyloidosis such as Alzheimer'"'"'s disease in a subject in need thereof, characterized in that it comprises administering an inhibitor of the interaction between Aβ globulomer and the P/Q type voltage-gated presynaptic calcium channel to said subject.
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Citations
3 Claims
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1. A method for the treatment of an amyloidosis disease comprising administering to a subject in need thereof an agent that inhibits the interaction between Aβ
- globulomer and P/Q type voltage-gated presynaptic calcium channel, wherein the agent is an antibody that binds to the P/Q type voltage-gated presynaptic calcium channel, wherein the amyloidosis disease is selected from the group consisting of Alzheimer'"'"'s disease and Down'"'"'s syndrome, wherein the antibody is raised against a peptide mapping near the C-terminus of the α
1A subunit of the P/Q type voltage-gated presynaptic calcium channel, and wherein the antibody is sc-16228. - View Dependent Claims (2, 3)
- globulomer and P/Q type voltage-gated presynaptic calcium channel, wherein the agent is an antibody that binds to the P/Q type voltage-gated presynaptic calcium channel, wherein the amyloidosis disease is selected from the group consisting of Alzheimer'"'"'s disease and Down'"'"'s syndrome, wherein the antibody is raised against a peptide mapping near the C-terminus of the α
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