Dual specificity antibody fusions

US9828438B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9828438-B2
Application numberUS-201615058460-A
CountryUS
Kind codeB2
Filing dateJul 6, 2016
Priority dateSep 26, 2007
Publication dateNov 28, 2017
Grant dateNov 28, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

The present invention provides dual specificity antibody fusion proteins comprising an antibody Fab or Fab′ fragment with specificity for an antigen of interest, said fragment being fused to at least one single domain antibody which has specificity for a second antigen of interest.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for the treatment of a disease or disorder, comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a dual specificity antibody fusion protein comprising an antibody Fab fragment or an antibody Fab′ fragment with specificity for an antigen of interest, the fragment being fused to two single domain antibodies that have specificity for serum albumin, wherein one single domain antibody is fused to a C-terminus of a light chain of the Fab fragment or the Fab′ fragment and the other single domain antibody is fused to a C-terminus of a heavy chain of the Fab fragment or the Fab′ fragment, and wherein one single domain antibody is a VH domain comprising the sequence given in SEQ ID NO: 56 for CDRH 1, the sequence given in SEQ ID NO: 57 for CDR-H2 and the sequence given in SEQ ID NO: 58 for CDR-H3, and the other single domain antibody is a VL domain comprising the sequence given in SEQ ID NO: 59 for CDR-L1, the sequence given in SEQ ID NO: 60 for CDR-L2 and the sequence given in SEQ ID NO: 61 for CDR-L3, wherein the VH domain is fused to the C-terminus of the heavy chain of the Fab fragment or the Fab′ fragment and the VL domain is fused to the C-terminus of the light chain of the Fab fragment or the Fab′ fragment. 2. The method of claim 1 , wherein the pharmaceutical composition additionally comprises other active ingredients and/or carriers. 3. The method of claim 1 , wherein each single domain antibody humanised. 4. The method of claim 1 , wherein the Fab or Fab′ is fully human or humanised. 5. The method of claim 1 , wherein each single domain antibody fused to the antibody Fab or Fab′ fragment is fused via a linker of the amino acid sequence SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 or SEQ ID NO: 45. 6. The method of claim 1 , in which the VH domain is linked to the C-terminus of the heavy chain of the Fab or Fab′ fragment via a linker having the sequence given in SEQ ID NO: 2 or SEQ ID NO: 45 and the VL domain is linked to the C-terminus of the light chain of the Fab or Fab′ fragment via a linker having the sequence given in SEQ ID NO: 1 or SEQ ID NO: 45. 7. The method of claim 1 , wherein the serum albumin is human serum albumin. 8. The method of claim 1 , wherein the disease or disorder is an inflammatory disease or disorder, an immune disease or disorder, a fibrotic disorder and/or a cancer; wherein the inflammatory disease or disorder and/or the immune disease or disorder comprise rheumatoid arthritis, psoriatic arthritis, still's disease, Muckle Wells disease, psoriasis, Crohn's disease, ulcerative colitis, SLE (Systemic Lupus Erythematosus), asthma, allergic rhinitis, atopic dermatitis, multiple sclerosis, vasculitis, Type I diabetes mellitus, transplantation and graft-versus-host disease; wherein the fibrotic disorder comprises idiopathic pulmonary fibrosis (IPF), systemic sclerosis (or scleroderma), kidney fibrosis, diabetic nephropathy, IgA nephropathy, hypertension, end-stage renal disease, peritoneal fibrosis (continuous ambulatory peritoneal dialysis), liver cirrhosis, age-related macular degeneration (ARMD), retinopathy, cardiac reactive fibrosis, scarring, keloids, burns, skin ulcers, angioplasty, coronary bypass surgery, arthroplasty and cataract surgery; and wherein the cancer comprises (i) a malignant new growth that arises from epithelium, found in skin or the lining of breast, ovary, prostate, lung, kidney, pancreas, stomach, bladder or bowel and/or (ii) bone, liver, lung or brain cancer.

Assignees

Inventors

Classifications

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • Antihypertensives · CPC title

  • Drugs for disorders of the cardiovascular system · CPC title

  • for hyperglycaemia, e.g. antidiabetics · CPC title

  • Antineoplastic agents · CPC title

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Frequently asked questions

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What does patent US9828438B2 cover?
The present invention provides dual specificity antibody fusion proteins comprising an antibody Fab or Fab′ fragment with specificity for an antigen of interest, said fragment being fused to at least one single domain antibody which has specificity for a second antigen of interest.
Who is the assignee on this patent?
Ucb Pharma Sa
What technology area does this patent fall under?
Primary CPC classification C07K16/468. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).