Anti-activin A antibodies and uses thereof

US11542325B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11542325-B2
Application numberUS-201816128831-A
CountryUS
Kind codeB2
Filing dateSep 12, 2018
Priority dateSep 8, 2006
Publication dateJan 3, 2023
Grant dateJan 3, 2023

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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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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The disclosure provides compositions and methods relating to or derived from anti-activin A binding proteins, including antibodies. In particular embodiments, the disclosure provides fully human, humanized, and chimeric anti-activin A antibodies that bind human activin A, activin A-binding fragments and derivatives of such antibodies, and activin A-binding polypeptides comprising such fragments. Other embodiments provide nucleic acids encoding such antibodies, antibody fragments and derivatives and polypeptides, cells comprising such polynucleotides, methods of making such antibodies, antibody fragments and derivatives and polypeptides, and methods of using such antibodies, antibody fragments and derivatives and polypeptides, including methods of treating or diagnosing subjects having activin A-related disorders or conditions including cachexia related to gonadal cancer, other cancers, rheumatoid arthritis, and other diseases.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of attenuating cachexia in a subject, comprising administering an effective amount of a pharmaceutically acceptable composition comprising a pharmaceutically acceptable excipient and an isolated antibody or antigen binding fragment thereof, comprising: a. a light chain variable domain (VL) comprising: i. a light chain CDR1 sequence of SEQ ID NO:11; ii. a light chain CDR2 sequence of SEQ ID NO:12; and iii. a light chain CDR3 sequence of SEQ ID NO:13; and b. a heavy chain variable domain (VH) comprising: i. a heavy chain CDR1 sequence of SEQ ID NO:62; ii. a heavy chain CDR2 sequence of SEQ ID NO:63; and iii. a heavy chain CDR3 sequence of SEQ ID NO:64. 2. A method of ameliorating the loss of body weight in a subject, comprising administering an effective amount of a pharmaceutically acceptable composition comprising a pharmaceutically acceptable excipient and an isolated antibody or antigen binding fragment thereof, comprising: a. a light chain variable domain (VL) comprising: i. a light chain CDR1 sequence of SEQ ID NO:11; ii. a light chain CDR2 sequence of SEQ ID NO:12; and iii. a light chain CDR3 sequence of SEQ ID NO:13; and b. a heavy chain variable domain (VH) comprising: i. a heavy chain CDR1 sequence of SEQ ID NO:62; ii. a heavy chain CDR2 sequence of SEQ ID NO:63; and iii. a heavy chain CDR3 sequence of SEQ ID NO:64. 3. A method of ameliorating the loss of muscle mass in a subject, comprising administering an effective amount of a pharmaceutically acceptable composition comprising a pharmaceutically acceptable excipient and an isolated antibody or antigen binding fragment thereof, comprising: a. a light chain variable domain (VL) comprising: i. a light chain CDR1 sequence of SEQ ID NO:11; ii. a light chain CDR2 sequence of SEQ ID NO:12; and iii. a light chain CDR3 sequence of SEQ ID NO:13; and b. a heavy chain variable domain (VH) comprising: i. a heavy chain CDR1 sequence of SEQ ID NO:62; ii. a heavy chain CDR2 sequence of SEQ ID NO:63; and iii. a heavy chain CDR3 sequence of SEQ ID NO:64. 4. A method of ameliorating the loss of fat mass in a subject, comprising administering an effective amount of a pharmaceutically acceptable composition comprising a pharmaceutically acceptable excipient and an isolated antibody or antigen binding fragment thereof, comprising: a. a light chain variable domain (VL) comprising: i. a light chain CDR1 sequence of SEQ ID NO:11; ii. a light chain CDR2 sequence of SEQ ID NO:12; and iii. a light chain CDR3 sequence of SEQ ID NO:13; and b. a heavy chain variable domain (VH) comprising: i. a heavy chain CDR1 sequence of SEQ ID NO:62; ii. a heavy chain CDR2 sequence of SEQ ID NO:63; and iii. a heavy chain CDR3 sequence of SEQ ID NO:64.

Assignees

Inventors

Classifications

  • comprising antibodies · CPC title

  • of the anterior pituitary hormones, e.g. TSH, ACTH, FSH, LH, PRL, GH · CPC title

  • Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title

  • Drugs for disorders of the endocrine system · CPC title

  • Anorexiants; Antiobesity agents · CPC title

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Frequently asked questions

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What does patent US11542325B2 cover?
The disclosure provides compositions and methods relating to or derived from anti-activin A binding proteins, including antibodies. In particular embodiments, the disclosure provides fully human, humanized, and chimeric anti-activin A antibodies that bind human activin A, activin A-binding fragments and derivatives of such antibodies, and activin A-binding polypeptides comprising such fragments…
Who is the assignee on this patent?
Amgen Inc
What technology area does this patent fall under?
Primary CPC classification A61P1/00. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jan 03 2023 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).