Methods for treating pancreatic cancer using combination therapies comprising liposomal irinotecan
US-9339497-B2 · May 17, 2016 · US
US9885087B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9885087-B2 |
| Application number | US-201514847304-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 8, 2015 |
| Priority date | Jul 5, 2011 |
| Publication date | Feb 6, 2018 |
| Grant date | Feb 6, 2018 |
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Anti-EGFR antibodies, therapeutic compositions comprising combinations of anti-EGFR antibodies, as well as methods for using such antibodies and compositions to treat EGFR-related disorders (e.g., cancers), are disclosed.
Opening claim text (preview).
What is claimed is: 1. A monoclonal antibody which binds EGFR extracellular domain and comprises heavy chain CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NOs: 13, 14, and 15, respectively, and light chain CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NOs: 16, 17 and 18, respectively. 2. A monoclonal antibody which binds EGFR extracellular domain and comprises a heavy chain variable region as set forth in SEQ ID NO: 23 and a light chain variable region as set forth in SEQ ID NO: 24. 3. The monoclonal antibody of claim 1 , wherein the antibody binds EGFR extracellular domain with a K D of better than 1 nM. 4. The monoclonal antibody of claim 1 , wherein the antibody is a human or humanized antibody. 5. The monoclonal antibody of claim 1 , wherein the antibody is an IgG1. 6. The monoclonal antibody of claim 2 , wherein the antibody is a human or humanized antibody. 7. The monoclonal antibody of claim 2 , wherein the antibody is an IgG1. 8. The monoclonal antibody of claim 3 , wherein the antibody is a human or humanized antibody. 9. The monoclonal antibody of claim 3 , wherein the antibody is an IgG1. 10. A composition comprising the monoclonal antibody of claim 1 and a pharmaceutically acceptable carrier. 11. The composition according to claim 10 , which is a sterile composition. 12. The composition according to claim 11 , which is formulated for intravenous injection. 13. A composition comprising the monoclonal antibody of claim 2 and a pharmaceutically acceptable carrier. 14. The composition according to claim 13 , which is a sterile composition. 15. The composition according to claim 14 , which is formulated for intravenous injection. 16. A composition comprising the monoclonal antibody of claim 3 and a pharmaceutically acceptable carrier. 17. The composition according to claim 16 , which is a sterile composition. 18. The composition according to claim 17 , which is formulated for intravenous injection. 19. A composition comprising the monoclonal antibody of claim 5 and a pharmaceutically acceptable carrier. 20. A composition comprising the monoclonal antibody of claim 7 and a pharmaceutically acceptable carrier. 21. A composition comprising the monoclonal antibody of claim 9 and a pharmaceutically acceptable carrier.
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