Antibody fragments against the insulin receptor and uses thereof to treat hypoglycemia
View Patent ↗The present disclosure relates, in general, to methods of treating or preventing hypoglycemia using a negative modulator antibody fragment that binds to the insulin receptor and modulates the action of insulin at the insulin receptor.
1. An antibody or fragment thereof comprising three heavy chain CDRs having the amino acid sequence set out in SEQ ID NOs: 5-7, 8-10 and 50-112 and three light chain CDRs have the amino acid sequences set out in SEQ ID NOs: 14-16 or SEQ ID NOs: 20-28 wherein the antibody or fragment thereof binds to i) insulin receptor or (ii) a complex comprising insulin and insulin receptor, or both (i) and (ii).
2. An antibody or fragment thereof of claim 1 wherein the heavy chain variable region amino acid sequence is set out in SEQ ID NOs: 1, 2 or 29-49, and the light chain variable region amino acid sequence is set out in SEQ ID NOs: 4 or 17-19.
3. The antibody fragment of claim 1 which is a Fab fragment.
4. The antibody or antibody fragment of claim 1 , wherein said antibody is a human antibody.
5. An antibody or fragment thereof comprising three heavy chain CDRs having the amino acid sequence set out in SEQ ID NOs: 8-10 and three light chain CDRs have the amino acid sequences set out in SEQ ID NOs: 14-16, wherein the antibody or fragment thereof binds to i) insulin receptor or (ii) a complex comprising insulin and insulin receptor, or both (i) and (ii).
6. The antibody or fragment thereof of claim 5 wherein the heavy chain variable region amino acid sequence is set out in SEQ ID NO: 2 and the light chain variable region amino acid sequence is set out in SEQ ID NO: 4.
7. The antibody fragment of claim 5 wherein the heavy chain variable region amino acid sequence is set out in SEQ ID NO: 1 or 2 and the light chain variable region amino acid sequence is set out in SEQ ID NO: 3 or 4.
8. An antibody fragment comprising three heavy chain CDRs having the amino acid sequences set out in SEQ ID NOs: 5-7 or 8-10 and three light chain CDRs having the amino acid sequences set out in SEQ ID NOs: 11-13 or 14-16, wherein the antibody fragment binds to i) insulin receptor or (ii) a complex comprising insulin and insulin receptor, or both (i) and (ii).
9. The antibody fragment of claim 8 or 7 wherein the three heavy chain CDRs have the amino acid sequences set out in SEQ ID NOs: 8-10 and three light chain CDRs have the amino acid sequences set out in SEQ ID NOs: 14-16.
10. The antibody fragment of claim 8 wherein the heavy chain variable region amino acid sequence is set out in SEQ ID NO: 2 and the light chain variable region amino acid sequences is set out in SEQ ID NO: 4.
11. A sterile composition comprising the antibody of any of one of claims 1 to 3 and 4 , and a sterile pharmaceutically acceptable diluent.
12. A method of treating hypoglycemia, comprising administering to a subject in need thereof an antibody fragment according to claim 1 , that is a negative modulator of insulin binding to the insulin receptor and/or insulin action at the insulin receptor in an amount effective to ameliorate hypoglycemia.
13. The method of claim 12 , wherein the hypoglycemia is selected from the group consisting of sulfonylurea-induced hypoglycemia, insulin-induced hypoglycemia, nocturnal hypoglycemia, hypoglycemia following post-bariatric surgery, and hypoglycemia in subjects with inherited metabolic and insulin sensitivity disorders.
14. A method for treating nocturnal hypoglycemia comprising administering to a subject in need thereof an antibody fragment according to claim 1 , that is a negative modulator of insulin binding to the insulin receptor and/or insulin action at the insulin receptor in an amount effective to ameliorate nocturnal hypoglycemia.
15. The method of any one of claims 12 to 14 wherein the antibody fragment comprises three heavy chain CDRs set out in SEQ ID NOs: 5-7, 8-10 or 50-112 and three light chain CDRs set out in SEQ ID NOs: 11-13, 14-16 or 20-28.
16. The method of any one of claims 12 to 14 , wherein the antibody fragment comprises a heavy chain variable region selected from the group consisting of SEQ ID NO: 1 or 2 and a light chain variable region selected from the group consisting of SEQ ID NO: 3 or 4.
17. The method of claim 14 , wherein the antibody fragment is from a human antibody.
18. The method of claim 14 , wherein the antibody fragment is a Fab fragment.
19. The method of claim 14 , wherein the antibody fragment reduces hyperinsulinemia or excess insulin signaling in the subject.
20. The method of claim 14 , wherein the subject has a blood glucose level of less than 70 mg/dL prior to administration.
21. The method of claim 14 , wherein the antibody fragment is administered at a dose of from 0.1 to 25 mg/kg.
22. The method of claim 14 , wherein the antibody fragment is administered in a single bolus, once every 12 hours or once per day, until hypoglycemia is eliminated.
23. The method of claim 14 , wherein the antibody is administered intravenously, intraarterially, intraperitoneally, intramuscularly, intradermally, subcutaneously or orally.
24. The method of claim 14 , wherein administration increases blood glucose in the subject by 1.5 to 10 fold or by 10 to 40%, optionally wherein administration increases blood glucose in the subject by at least 10 mg/dL.
25. The method of claim 14 , wherein the subject is also on a restricted diet regimen.
26. The method of claim 14 , further comprising administering a second agent.
27. The method of claim 14 , wherein the administration ameliorates one or more symptoms of hypoglycemia selected from the group consisting of pancreatic nesidioblastosis, islet cell enlargement, islet cell hyperplasia, β cell budding, tachycardia, diaphoresis, flushing and reduced cognitive function.
28. The method of claim 14 , wherein the administration reduces or eliminates hypoglycemia within 20 minutes.
29. The method of claim 14 , wherein the antibody fragment has a duration of action of approximately 4 hours.
30. The method of claim 14 , wherein the subject is non-responsive to dextrose or glucagon therapy.
31. The method of claim 14 , wherein the administration reduces or eliminates hypoglycemia within 15 minutes.
32. The method of claim 26 , wherein the second agent is glucagon and/or insulin.
33. A method of preparing a sterile pharmaceutical composition, comprising adding a sterile pharmaceutically acceptable diluent to an antibody of any one of claims 1 - 3 and 4 .