Antibody therapeutics that bind CD38

US11999792B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11999792-B2
Application numberUS-202017016104-A
CountryUS
Kind codeB2
Filing dateSep 9, 2020
Priority dateApr 8, 2015
Publication dateJun 4, 2024
Grant dateJun 4, 2024

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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.

There is disclosed compositions and methods relating to or derived from anti-CD38 antibodies. More specifically, there is disclosed fully human antibodies that bind CD38, CD38-antibody binding fragments and derivatives of such antibodies, and CD38-binding polypeptides comprising such fragments. Further still, there is disclosed 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 a disease.

First claim

Opening claim text (preview).

We claim: 1. One or more nucleic acids encoding an antibody of an IgG class that binds to a CD38 epitope, wherein said antibody comprises (i) a heavy chain variable domain sequence comprising the amino acid sequence of SEQ ID NO: 3; and a light chain variable domain sequence comprising the amino acid sequence of SEQ ID NO: 4; or (ii) a heavy chain variable domain comprising CDR1, CDR2, and CDR3 of the amino acid sequence of SEQ ID NO: 3 and a light chain variable domain comprising CDR1, CDR2, and CDR3 of the amino acid sequence of SEQ ID NO: 4. 2. The one or more nucleic acids of claim 1 , wherein said antibody comprises the heavy chain variable domain sequence comprising the amino acid sequence of SEQ ID NO: 3 and the light chain variable domain sequence comprising the amino acid sequence of SEQ ID NO: 4. 3. The one or more nucleic acids of claim 1 , wherein the antibody is an IgG1 antibody. 4. The one or more nucleic acids of claim 1 , wherein the antibody is an IgG4 antibody. 5. The one or more nucleic acids of claim 1 , wherein the antibody is a full-length antibody. 6. The one or more nucleic acids of claim 1 , wherein the antibody is an antibody fragment or single chain antibody comprising the heavy chain variable domain sequence and the light chain variable domain sequence. 7. The one or more nucleic acids of claim 6 , wherein the antibody fragment or single chain antibody is a Fab or F(ab')2 fragment or an scFv. 8. The one or more nucleic acids of claim 1 , wherein the antibody binds CD38 with a binding affinity of at least 10 −6 M. 9. The one or more nucleic acids of claim 1 , wherein the antibody binds CD38 with a binding affinity of at least 10 −8 M. 10. The one or more nucleic acids of claim 2 , wherein the antibody is an IgG1 antibody. 11. The one or more nucleic acids of claim 2 , wherein the antibody is an antibody fragment or single chain antibody comprising the heavy chain variable domain sequence and the light chain variable domain sequence. 12. The one or more nucleic acids of claim 2 , wherein the antibody is an IgG4 antibody. 13. The one or more nucleic acids of claim 2 , wherein the antibody binds CD38 with a binding affinity of at least 10 −6 M. 14. The one or more nucleic acids of claim 2 , wherein the antibody binds CD38 with a binding affinity of at least 10 −8 M. 15. The one or more nucleic acids of claim 1 , wherein the antibody comprises a heavy chain variable domain comprising the amino acid sequence that is at least 95% identical to SEQ ID NO: 3, a light chain variable domain comprising the amino acid sequence that is at least 95% identical to SEQ ID NO: 4, three heavy chain complementarity determining regions (CDRs) as set forth in the heavy chain variable domain amino acid sequence of SEQ ID NO: 3, and three light chain CDRs as set forth in the light chain variable domain amino acid sequence of SEQ ID NO: 4. 16. One or more vectors comprising the one or more nucleic acids of claim 1 . 17. A host cell comprising the one or more nucleic acids of claim 1 . 18. A host cell comprising the one or more vectors of claim 16 . 19. A method of producing an antibody, comprising culturing the cell of claim 17 under conditions wherein the antibody is produced. 20. A method of producing an antibody, comprising culturing the cell of claim 18 under conditions wherein the antibody is produced.

Assignees

Inventors

Classifications

  • Medicinal preparations containing antigens or antibodies (materials for immunoassay G01N33/53) · CPC title

  • against molecules with a "CD"-designation, not provided for elsewhere · CPC title

  • Antibodies (agglutinins A61K38/36 {; as drug carriers A61K47/50}); Immunoglobulins; Immune serum, e.g. antilymphocytic serum · CPC title

  • against tumor tissues, cells, antigens · CPC title

  • against enzymes · CPC title

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Frequently asked questions

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What does patent US11999792B2 cover?
There is disclosed compositions and methods relating to or derived from anti-CD38 antibodies. More specifically, there is disclosed fully human antibodies that bind CD38, CD38-antibody binding fragments and derivatives of such antibodies, and CD38-binding polypeptides comprising such fragments. Further still, there is disclosed nucleic acids encoding such antibodies, antibody fragments and deri…
Who is the assignee on this patent?
Sorrento Therapeutics Inc, Vivasor Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/2896. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 04 2024 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 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).