Anti-hemojuvelin (hjv) antibodies for treating myelofibrosis
US-2023174645-A1 · Jun 8, 2023 · US
US12098192B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12098192-B2 |
| Application number | US-202418638307-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 17, 2024 |
| Priority date | Dec 14, 2011 |
| Publication date | Sep 24, 2024 |
| Grant date | Sep 24, 2024 |
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Provided herein are methods of using the antibodies that bind to RGMc to treat and diagnose iron-related disorders.
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We claim: 1. A composition comprising an anti-Repulsive Guidance Molecule c (RGMc) antibody that comprises: (i) a variable heavy chain region comprising a complementary determining region (CDR)1 with the amino acid sequence set forth in SEQ ID NO: 17, a CDR2 with the amino acid sequence set forth in SEQ ID NO: 18, a CDR3 with the amino acid sequence set forth in SEQ ID NO: 19, and a variable light chain region comprising a CDR1 with the amino acid sequence set forth in SEQ ID NO: 20, a CDR2 with the amino acid sequence set forth in SEQ ID NO: 21, and a CDR3 with the amino acid sequence set forth in SEQ ID NO:22; and (ii) a human IgG1 constant domain. 2. The composition of claim 1 , wherein the antibody is affinity matured. 3. The composition of claim 1 , wherein the variable light chain region has the amino acid sequence set forth in SEQ ID NO: 6. 4. The composition of claim 1 , wherein the variable heavy chain region has the amino acid sequence set forth in SEQ ID NO: 5 with up to one amino acid difference in a framework region. 5. The composition of claim 3 , wherein the variable heavy chain region has the amino acid sequence set forth in SEQ ID NO: 5 with up to one amino acid difference in a framework region. 6. The composition of claim 1 , further comprising a pharmaceutically acceptable carrier. 7. The composition of claim 1 , wherein the composition is in a lyophilized form. 8. The composition of claim 1 , wherein the composition is in a solution form. 9. The composition of claim 5 , wherein the composition is in a lyophilized form. 10. The composition of claim 5 , wherein the composition is in a solution form. 11. A composition comprising an anti-Repulsive Guidance Molecule c (RGMc) antibody that comprises: a variable heavy chain region linked to a heavy chain constant domain, the heavy chain variable region comprises a complementary determining region (CDR)1 comprising the amino acid sequence set forth in SEQ ID NO: 17, a CDR2 comprising the amino acid sequence set forth in SEQ ID NO: 18, a CDR3 comprising the amino acid sequence set forth in SEQ ID NO: 19, and a variable light chain region linked to a light chain constant domain, the light chain variable region comprises a CDR1 comprising the amino acid sequence set forth in SEQ ID NO: 20, a CDR2 comprising the amino acid sequence set forth in SEQ ID NO: 21, and a CDR3 comprising the amino acid sequence set forth in SEQ ID NO:22. 12. The composition of claim 11 , wherein the antibody is affinity matured. 13. The composition of claim 11 , wherein the variable light chain region has the amino acid sequence set forth in SEQ ID NO: 6. 14. The composition of claim 11 , wherein the variable heavy chain region has the amino acid sequence set forth in SEQ ID NO: 5 with up to one amino acid difference in a framework region. 15. The composition of claim 13 , wherein the variable heavy chain region has the amino acid sequence set forth in SEQ ID NO: 5 with up to one amino acid difference in a framework region. 16. The composition of claim 11 , further comprising a pharmaceutically acceptable carrier. 17. The composition of claim 11 , wherein the composition is in a lyophilized form. 18. The composition of claim 11 , wherein the composition is in a solution form. 19. The composition of claim 15 , wherein the composition is in a lyophilized form. 20. The composition of claim 15 , wherein the composition is in a solution form.
comprising antibodies · CPC title
against receptors, cell surface antigens or cell surface determinants · CPC title
Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title
Complementarity determining region [CDR] · CPC title
containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title
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