Human antigen binding proteins that bind to a complex comprising β-Klotho and an FGF receptor

US9574002B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9574002-B2
Application numberUS-201213487061-A
CountryUS
Kind codeB2
Filing dateJun 1, 2012
Priority dateJun 6, 2011
Publication dateFeb 21, 2017
Grant dateFeb 21, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention provides compositions and methods relating to or derived from antigen binding proteins capable of inducing B-Klotho, and or FGF21-like mediated signaling.

First claim

Opening claim text (preview).

What is claimed is: 1. An isolated antigen binding protein that induces FGF21-mediated signaling, wherein the antigen binding protein comprises a light chain CDR1 comprising the sequence of SEQ ID NO: 821, a light chain CDR2 comprising the sequence of SEQ ID NO: 900, a light chain CDR3 comprising the sequence of SEQ ID NO: 954, a heavy chain CDR1 comprising the sequence of SEQ ID NO: 611, a heavy chain CDR2 comprising the sequence of SEQ ID NO: 664, and a heavy chain CDR3 comprising the sequence of SEQ ID NO: 741. 2. The antigen binding protein of claim 1 , comprising one or more of: (a) a light chain variable domain sequence comprising V L 47 of Table 2A (SEQ ID NO. 263); (b) a heavy chain variable domain sequence comprising V H 46 of Table 2B (SEQ ID NO: 361); or (c) a combination comprising a light chain variable domain of (a) and a heavy chain variable domain of (b). 3. The antigen binding protein of claim 2 , wherein the light chain variable domain and the heavy chain variable domain comprise V L 47 and V H 46. 4. The antigen binding protein of claim 3 , further comprising: (a) the kappa light chain constant sequence of SEQ ID NO: 12 (b) the lambda light chain constant sequence of SEQ ID NO: 13 (c) the heavy chain constant sequence of SEQ ID NO: 11; or (d) (i) the kappa light chain constant sequence of SEQ ID NO: 12 or the lambda light chain constant sequence of SEQ ID NO: 13, and (ii) the heavy chain constant sequence of SEQ ID NO: 11. 5. The antigen binding protein of claim 1 , wherein the antigen binding protein is a human antibody, a humanized antibody, chimeric antibody, a monoclonal antibody, a polyclonal antibody, a recombinant antibody, an antigen-binding antibody fragment, a single chain antibody, a diabody, a triabody, a tetrabody, a Fab fragment, an F(fab′) 2 fragment, an IgD antibody, an IgE antibody, an IgM antibody, an IgG1 antibody, an IgG2 antibody, an IgG3 antibody, an IgG4 antibody, or an IgG4 antibody having at least one mutation in the hinge region. 6. A pharmaceutical composition comprising one or more antigen binding proteins of claim 1 , 2 , 3 , 4 or 5 in admixture with a pharmaceutically acceptable carrier thereof. 7. The antigen binding protein of claim 1 , wherein the antigen binding protein comprises one or more non-naturally occurring or encoded amino acids. 8. A method of treating a condition in a subject in need of such treatment comprising administering a therapeutically effective amount of the composition of claim 6 to the subject, wherein the condition is treatable by lowering one or more of blood glucose, insulin or serum lipid levels. 9. The method of claim 8 , wherein the condition is type 2 diabetes, obesity, dyslipidemia, NASH, cardiovascular disease or metabolic syndrome. 10. An isolated nucleic acid comprising a polynucleotide sequence encoding the light chain variable domain amino acid sequence, the heavy chain variable domain amino acid sequence, or both amino add sequences, of an antigen binding protein that induces FGF21-mediated signaling, wherein the antigen binding protein comprises a light chain CDR1 comprising the sequence of SEQ ID NO: 821, a light chain CDR2 comprising the sequence of SEQ ID NO: 900, a light chain CDR3 comprising the sequence of SEQ ID NO: 954, a heavy chain CDR1 comprising the sequence of SEQ ID NO: 611, a heavy chain CDR2 comprising the sequence of SEQ ID NO: 664, and a heavy chain CDR3 comprising the sequence of SEQ ID NO: 741. 11. An expression vector comprising the nucleic acid of claim 10 . 12. An isolated cell comprising the nucleic acid of claim 11 . 13. An isolated cell comprising the expression vector of claim 12 . 14. A method of producing an antigen binding protein comprising incubating the host cell of claim 13 under conditions that allow it to express the antigen binding protein.

Assignees

Inventors

Classifications

  • Drugs for disorders of the cardiovascular system · CPC title

  • Antihyperlipidemics · CPC title

  • for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

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

  • Drugs for disorders of the metabolism (of the blood or the extracellular fluid A61P7/00) · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9574002B2 cover?
The present invention provides compositions and methods relating to or derived from antigen binding proteins capable of inducing B-Klotho, and or FGF21-like mediated signaling.
Who is the assignee on this patent?
Li Yang, Stevens Jennitte, King Chadwick Terence, and 5 more
What technology area does this patent fall under?
Primary CPC classification C07K16/2863. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 21 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).