Agents, uses and methods for the treatment of synucleinopathy
US-2018194833-A1 · Jul 12, 2018 · US
US10364286B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10364286-B2 |
| Application number | US-201715848999-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2017 |
| Priority date | Dec 22, 2016 |
| Publication date | Jul 30, 2019 |
| Grant date | Jul 30, 2019 |
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The invention relates to a novel use of monoclonal anti-alpha-synuclein antibodies. The antibodies can be used to prevent tau aggregation and thereby treating tauopathies such as Alzheimer's disease.
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The invention claimed is: 1. A method for treating Alzheimer's disease without Lewy body pathology in a patient comprising: providing a monoclonal antibody, or an antigen-binding fragment thereof, that specifically binds alpha-synuclein to a patient having Alzheimer's disease without Lewy body pathology in an amount effective to inhibit aggregation of tau in the patient, wherein: (i) the antibody, or antigen-binding fragment thereof, comprises: a Heavy Chain CDR1 having the amino acid sequence of SEQ ID NO:1; a Heavy Chain CDR2 having the amino acid sequence selected from SEQ ID NO:2, SEQ ID NO:33, SEQ ID NO:34, or SEQ ID NO:35; a Heavy Chain CDR3 having the amino acid sequence of SEQ ID NO:3; a Light Chain CDR1 having the amino acid sequence of SEQ ID NO:4; a Light Chain CDR2 having the amino acid sequence of SEQ ID NO:5; and a Light Chain CDR3 having the amino acid sequence of SEQ ID NO:6; or (ii) the antibody, or antigen-binding fragment thereof, comprises: a Heavy Chain CDR1 having the amino acid sequence of SEQ ID NO:20; a Heavy Chain CDR2 having the amino acid sequence of SEQ ID NO:21; a Heavy Chain CDR3 having the amino acid sequence of SEQ ID NO:22; a Light Chain CDR1 having the amino acid sequence of SEQ ID NO:23; a Light Chain CDR2 having the amino acid sequence of SEQ ID NO:24; and a Light Chain CDR3 having the amino acid sequence of SEQ ID NO:25. 2. The method of claim 1 , wherein the antibody binds aggregated soluble forms of alpha-synuclein. 3. The method of claim 1 , wherein the patient does not have Lewy body variant of Alzheimer's disease or combined Parkinson and Alzheimer's disease. 4. The method of claim 1 , wherein said antibody or antigen-binding fragment thereof binds to the C-terminal part of alpha-synuclein. 5. The method of claim 4 , wherein the antibody or antigen-binding fragment thereof binds to an epitope within the C-terminal amino acids 110-140 of human alpha-synuclein (SEQ ID NO 10). 6. The method of claim 4 , wherein said epitope is within amino acids 112-117, 112-115, 118-126, 126-138 or 136-140 of human alpha-synuclein (SEQ ID NO 10). 7. A pharmaceutical composition comprising the monoclonal antibody, or antigen-binding fragment thereof, according to claim 1 , and a pharmaceutical acceptable carrier.
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