Glucose-regulating polypeptides and methods of making and using same
The present invention relates to compositions comprising glucose regulating peptides linked to extended recombinant polypeptide (XTEN), isolated nucleic acids encoding the compositions and vectors and host cells containing the same, and methods of making and using such compositions in treatment of glucose regulating peptide-related diseases, disorders, and conditions.
1. A kit comprising a pharmaceutical composition for use in treating a glucose regulating peptide-related condition in a subject, wherein the kit comprises
(a) a first container;
(b) the pharmaceutical composition comprising:
(i) a fusion protein comprising a glucose regulating peptide that is at least 90% identical to a glucose regulating peptide sequence selected from Tables 1-3, wherein said glucose regulating peptide is linked to an extended recombinant polypeptide (XTEN), wherein the XTEN sequence exhibits at least 90% sequence identity to a sequence selected from Table 5; and
ii) an amount of a pharmaceutically acceptable carrier.
2. The kit of claim 1 , wherein the glucose regulating peptide-related condition is selected from the group consisting of juvenile diabetes, type I diabetes, type II diabetes, obesity, acute hypoglycemia, acute hyperglycemia, nocturnal hypoglycemia, chronic hyperglycemia, glucagonomas, secretory disorders of the airway, arthritis, osteoporosis, central nervous system disease, restenosis, neurodegenerative disease, renal failure, congestive heart failure nephrotic syndrome, cirrhosis, hypertension, irritable bowel syndrome, myocardial infarction, post-surgical catabolic changes, diabetic cardiomyopathy, insufficient urinary sodium excretion, excessive urinary potassium concentration, polycystic ovary syndrome, respiratory distress, nephropathy, left ventricular systolic dysfunction, gastrointestinal disorders, postoperative dumping syndrome, irritable bowel syndrome, dyslipidemia, and critical illness polyneuropathy (CIPN).
3. The kit of claim 1 , wherein the fusion protein comprises a glucose regulating peptide that is at least 90% identical to SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, or SEQ ID NO:10 linked to an XTEN, wherein the XTEN sequence is at least 90% identical to a sequence selected from SEQ ID NO: 189, SEQ ID NO: 190, SEQ ID NO: 191, SEQ ID NO: 192, SEQ ID NO: 193, SEQ ID NO: 194, SEQ ID NO: 195, SEQ ID NO: 196, SEQ ID NO: 197, SEQ ID NO: 198, SEQ ID NO: 199, SEQ ID NO: 200, SEQ ID NO: 201, SEQ ID NO: 202, SEQ ID NO: 203, SEQ ID NO: 204, SEQ ID NO: 205, SEQ ID NO: 206, or SEQ ID NO: 207.
4. The kit of claim 3 , wherein the glucose regulating peptide of the fusion protein is at least 90% identical to the amino acid sequence SEQ ID NO:4.
5. The kit of claim 3 , wherein the glucose regulating peptide of the fusion protein is at least 90% identical to the amino acid sequence SEQ ID NO:5.
6. The kit of claim 3 , wherein the glucose regulating peptide of the fusion protein is at least 90% identical to the amino acid sequence SEQ ID NO:6.
7. The kit of claim 3 , wherein the glucose regulating peptide of the fusion protein is at least 90% identical to the amino acid sequence SEQ ID NO:10.
8. The kit of claim 3 , wherein the XTEN sequence is at least 90% identical to SEQ ID NO:189, SEQ ID NO:191, SEQ ID NO: 195, or SEQ ID NO:199.
9. The kit of claim 1 , wherein the fusion protein is at least 90% identical to SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 890, SEQ ID NO: 896, SEQ ID NO: 979, SEQ ID NO: 980, SEQ ID NO: 983, or SEQ ID NO: 986.
10. The kit of claim 1 , wherein the fusion protein comprises the sequence of SEQ ID NO: 896.
11. The kit of any one of claim 1 or claim 9 , comprising a second container that can carry a suitable diluent for the pharmaceutical composition, and a sheet of instructions for the reconstitution and/or administration of the pharmaceutical composition to a subject.
12. A syringe comprising a pharmaceutical composition for use in treating a glucose regulating peptide-related condition in a subject, wherein the pharmaceutical composition is supplied as a liquid in a pre-filled syringe, the pharmaceutical composition comprising:
(a) a fusion protein comprising a glucose regulating peptide that is at least 90% identical to a glucose regulating peptide sequence selected from Tables 1-3, wherein said glucose regulating peptide is linked to an extended recombinant polypeptide (XTEN), wherein the XTEN sequence exhibits at least 90% sequence identity to a sequence selected from Table 5; and
(b) an amount of a pharmaceutically acceptable carrier in the liquid.
13. The syringe of claim 12 , wherein the liquid formulation is an aqueous formulation.
14. The syringe of claim 12 , wherein the liquid formulation is capable of passing through a needle of gauge size 25 to 32 for administration to the subject.
15. The syringe of claim 12 , wherein the syringe is for administration of the pharmaceutical composition to a subject via a route selected from the group consisting of intravenous, intramuscular, intraarticular, and subcutaneous.
16. The syringe of any one of claims 12 - 15 , wherein the fusion protein is at least 90% identical to SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 890, SEQ ID NO: 896, SEQ ID NO: 979, SEQ ID NO: 980, SEQ ID NO: 983, or SEQ ID NO: 986.
17. The syringe of claim 16 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 896.