Antibodies to amyloid beta
US-10662239-B2 · May 26, 2020 · US
US12098191B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12098191-B2 |
| Application number | US-202217673449-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 16, 2022 |
| Priority date | Oct 15, 2012 |
| Publication date | Sep 24, 2024 |
| Grant date | Sep 24, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Antibody for human amyloid beta. Antibody selectively binds human amyloid beta 42 peptide over human amyloid beta 40 peptide. Antibodies specific for amyloid beta 42 as therapeutic agents for binding amyloid beta 42 peptide and treating conditions associated with amyloidosis, such as Alzheimer's disease.
Opening claim text (preview).
What is claimed is: 1. An isolated antibody molecule that is selective for binding human amyloid beta 1-42 peptide (Aβ1-42) over human amyloid beta 1-40 peptide (Aβ1-40), wherein the antibody molecule comprises a V H domain having an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 524 and a V L domain having an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 533, wherein the V H domain of the antibody molecule comprises: a) HCDR1 of SEQ ID NO: 525, HCDR2 of SEQ ID NO: 526, and HCDR3 of SEQ ID NO: 527; b) wherein FW1 of the V H domain comprises: a methionine residue at the amino acid position corresponding to position 26 of SEQ ID NO: 524; a glycine residue at the amino acid position corresponding to position 27 of SEQ ID NO: 524; an asparagine residue at the amino acid position corresponding to position 28 of SEQ ID NO: 524; and an asparagine residue at the amino acid position corresponding to position 30 of SEQ ID NO: 524; and wherein the V L domain of the antibody molecule comprises LCDR1 of SEQ ID NO: 534, LCDR2 of SEQ ID NO: 535, and LCDR3 of SEQ ID NO: 536. 2. The isolated antibody molecule of claim 1 , wherein the antibody molecule comprises a VH domain having an amino acid sequence that is at least 95%, 98% or 99% identical to the amino acid sequence of SEQ ID NO: 524 and a VL domain having an amino acid sequence that is at least 95%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 533. 3. The isolated antibody molecule of claim 1 , wherein the antibody molecule is a monoclonal antibody. 4. The isolated antibody molecule of claim 3 , wherein the monoclonal antibody is a recombinant antibody, a humanized antibody, a human antibody, a multispecific antibody, or an antibody fragment thereof. 5. The isolated antibody molecule of claim 4 , wherein the antibody molecule is an scFv. 6. The isolated antibody molecule of claim 4 , wherein the antibody molecule is a Fab. 7. The isolated antibody molecule of claim 3 , wherein the antibody molecule is of the IgG1-, IgG2-, or IgG4-type. 8. The isolated antibody molecule of claim 1 , wherein the antibody molecule is a chimeric antibody. 9. A composition comprising an isolated antibody molecule according to claim 1 , and a pharmaceutically acceptable excipient. 10. A method of treating a human or animal subject having an amyloidosis associated with amyloid beta, the method comprising administering to the subject an antibody according to claim 1 . 11. The method of claim 10 , wherein the treatment at least reduces amyloidosis; treats Alzheimer's disease; improves cognition or reduces cognitive decline in an Alzheimer's disease or Down's syndrome patient; or treats macular degeneration. 12. A method of at least reducing amyloidosis, treating Alzheimer's disease; improving cognition or reducing cognitive decline in an Alzheimer's disease or Down's syndrome patient; and/or treating macular degeneration in an individual, the method comprising administering to the subject an antibody according to claim 1 .
characterized by non-natural combinations of immunoglobulin fragments · CPC title
Framework region [FR] · CPC title
Complete light chain, i.e. VL + CL · CPC title
Complete heavy chain or Fd fragment, i.e. VH + CH1 · CPC title
comprising antibodies · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.