Immunoglobulin fusion proteins and compositions thereof
US-2016237156-A1 · Aug 18, 2016 · US
US11161891B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11161891-B2 |
| Application number | US-201616060384-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 9, 2016 |
| Priority date | Dec 9, 2015 |
| Publication date | Nov 2, 2021 |
| Grant date | Nov 2, 2021 |
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Disclosed herein are relaxin immunoglobulin fusion proteins useful for the treatment or prevention of a disease or condition in a subject.
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What is claimed is: 1. An immunoglobulin fusion protein comprising a therapeutic peptide inserted into a light chain complementarity determining region 3 (CDR3) of an antibody variable region comprising: a heavy chain comprising a CDR1 of SEQ ID NO: 72, a CDR2 of SEQ ID NO: 73, and a CDR3 sequence selected from SEQ ID NOS: 75-78; and a light chain comprising a CDR1 of SEQ ID NO: 89, a CDR2 of SEQ ID NO: 90, and a CDR3 sequence comprising at least three contiguous amino acids of SEQ ID NO: 91. 2. The immunoglobulin fusion protein of claim 1 , comprising SEQ ID NO: 75: SMITX(1)X(2)X(3)FDV; wherein X(1) is F, A, G, or P; X(2) is G, A, S, T, or P; and X(3) is G, A, V, L, or P. 3. The immunoglobulin fusion protein of claim 2 , wherein X(1) is F. 4. The immunoglobulin fusion protein of claim 2 , wherein X(2) is G. 5. The immunoglobulin fusion protein of claim 2 , wherein X(3) is G. 6. The immunoglobulin fusion protein of claim 1 , wherein the sequence selected from SEQ ID NOS: 75-78 comprises a sequence selected from SEQ ID NOS: 79-88. 7. The immunoglobulin fusion protein of claim 6 , comprising the SEQ ID NO: 79. 8. A method comprising administering to a subject in need thereof the immunoglobulin fusion protein of claim 1 . 9. An antibody comprising the immunoglobulin fusion protein of claim 1 and a Fc domain at least 90% homologous to SEQ ID NO: 98. 10. The antibody of claim 9 , comprising SEQ ID NO: 16. 11. An antibody comprising a Fc region having SEQ ID NO: 98, and an antibody variable region comprising a heavy chain comprising a sequence at least about 95% identical to SEQ ID NO: 16, and a light chain comprising a therapeutic peptide and a sequence at least about 95% identical to SEQ ID NO: 9. 12. The antibody of claim 11 , wherein the therapeutic peptide is positioned within the antibody variable region. 13. The antibody of claim 11 , wherein the therapeutic peptide is inserted into the antibody variable region.
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containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title
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