Claims for Patent: 8,394,367

Summary for Patent: 8,394,367

Title:	IL6R/IL6 chimera for therapy of chemotherapy-induced peripheral neuropathy
Abstract:	The invention relates to the use of IL-6R/IL-6 chimera in chemotherapy induced neuropathy.
Inventor(s):	Revel; Michel (Rehovot, IL), Chebath; Judith (Rehovot, IL), Krug; Hagit (Bar Yam, IL)
Assignee:	Yeda Research and Development Co., Ltd. (Rehovot, IL)
Application Number:	11/579,034
Patent Claims:	1. A method for treating and/or inhibiting Chemotherapy Induced Peripheral Neuropathy (CIPN), comprising administering to a patient in need thereof an effective amount of an IL6R/IL6 chimeric agent which is a) a chimera comprising a soluble IL6R moiety and an IL6 moiety, said soluble IL6R moiety comprising the cytokine receptor domain (amino acids 113 to 323 of SEQ ID NO:1) of the extracellular fragment of IL6R (gp80), and said IL6 moiety being a mature human IL6 (amino acids 28 to 212 of SEQ ID NO:2) or a contiguous fragment thereof, said IL6 moiety having IL6R binding activity and IL6R-mediated gp130 binding activity, and said soluble IL6R moiety having gp130-dimerizing activity, b) a mutein comprising an amino acid sequence that is (i) at least 80% identical to a chimera of (a), (ii) at least 80% identical to a chimera of (a) but that differs from said chimera of (a) solely by (a') one or more amino acid, substitutions, and/or (b') one or more amino acid insertions or deletions, hut the total number of insertions and deletions is under 30 amino acids, c) a derivative of (a) or (b), wherein (a) or (b) is derivatized by one or more derivatizations selected from the group consisting of an aliphatic ester derivative of a carboxyl group, an amide derivative of a carboxyl group, an N-acyl derivative of a free amino group, an O-acyl derivative of a free hydroxyl group, and PEGylation of a functional group of an amino acid residue comprised by said agent, or d) a salt of (a), (b), or (C), wherein said CIPN is not induced by administration of streptozotocin, wherein said agent has gp130 binding and gp130-dimerizing activity, optionally together with a pharmaceutically acceptable carrier, wherein at the time of administration of the chimeric agent, the patient is not suffering from diabetic neuropathy. 2. The method according to claim 1, wherein the CIPN is caused by chemotherapy agents selected from the group consisting of cisplatin, dicarbazine, streptozocin, cyclophosphamide, carmustine, lomustine, procarbazine, mitomycin, cytarabine, methotrexate, 5-fluorouracil, vinblastine, vincristine, bleomycin, paclitaxel, asparaginase, busulfan, carboplatin, dacarbazine, fludarabine, hydroxyurea, ifosfamide, mercaptopurine, mitotane, taxol and or a mixture of two or more agents thereof. 3. The method according to claim 2, wherein the chemotherapy agent is vinblastine or vincristine. 4. The method according to claim 1, wherein the chimeric agent is glycosylated at one or more sites. 5. The method according to claim 1, wherein the chimeric agent is non-glycosylated. 6. The method according to claim 1, wherein the agent is a PEGylated derivative. 7. The method according to claim 1, wherein the agent is administered by administering an expression vector comprising the coding sequence of said agent under conditions conducive to expression of said agent in said patient. 8. The method according to claim 7, wherein the vector is a lentiviral vector. 9. A method according to claim 1, wherein the administration is selected from the group consisting of intramuscular, intraperitoneal, intravenous, subcutaneous, and, topical routes. 10. The method of claim 1, wherein said chimeric agent is administered to said patient simultaneously with administration of a chemotherapeutic agent other than streptozotocin. 11. The method according to claim 10, wherein the chemotherapeutic agent is selected from the group consisting of cisplatin, dicarbazine, cyclophosphamide, carmustine, lomustine, procarbazine, mitomycin, cytarabine, methotrexate, 5-fluorouracil, vinblastine, vincristine, bleomycin, paclitaxel, asparaginase, busulfan, carboplatin, dacarbazine, fludarabine, hydroxyurea, ifosfamide, mercaptopurine, mitotane, streptozocin, taxol and a mixture of two or more agents thereof. 12. The method according to claim 11, wherein the chemotherapeutic agent comprises vincristine. 13. The method according to claim 1 wherein the chimeric agent is a fused protein comprising the IL6R/IL6 chimera of (a), or the mutein of (b), fused to an immunoglobulin or fragment thereof, or a derivative according to (c) of such a fused protein, or a salt of said fused protein or derivative thereof. 14. The method according to claim 1 wherein the mutein of (b) is at least 90% identical to a chimera of (a). 15. The method according to claim 1 wherein the chimera of (a) comprises a mature human IL6. 16. The method according to claim 1 wherein the moieties of the chimera of (a) are fused directly to one another. 17. The method according to claim 1 wherein the moieties of the chimera of (a) are connected by a linker amino acid or a linker peptide consisting of not more than 18 amino acids. 18. The method according to claim 1 wherein said mutein of (b) comprises an amino acid sequence that differs from a chimera of (a) solely by one or more amino acid substitutions. 19. The method according to claim 1 wherein said mutein of (b) comprises an amino acid sequence that differs from a chimera of (a) solely by one or more conservative substitutions. 20. The method of claim 1 wherein the chimeric agent is a chimera according to (a) or a derivative according to (c) thereof, or a salt of said chimera or derivative thereof. 21. The method of claim 1 wherein the chimeric agent is a chimera according to (a) or a salt thereof. 22. The method of claim 1 which is a method of treatment. 23. The method of claim 22 wherein the chimeric agent is administered by providing a composition comprising said chimeric agent and administering said composition to the patient. 24. The method of claim 1 wherein the agent is a chimera selected from the group consisting of SEQ ID NOs:3-5, or a derivative according to (c) thereof, or a salt of said chimera or derivative thereof. 25. The method of claim 1 wherein said IL6 moiety is human IL6 or a contiguous fragment thereof that differs from human IL6 by less than 10 amino acid deletions. 26. The method of claim 1 wherein at the time of administration of the chimeric agent, the patient is not suffering from diabetes. 27. The method of claim 1, wherein the differences between said fragment of human IL-6 and mature human IL-6 consist solely of deletion of one or more residues preceding the first alpha helix of mature human IL-6. 28. The method of claim 1, wherein said soluble IL6R moiety comprises amino acids 20-356 of SEQ ID NO:1. 29. The method of claim 28, wherein said agent is a chimera according to (a) or a derivative according to (c) thereof, or a salt of said chimera or derivative. 30. The method of claim 1, wherein said IL-6 moiety comprises amino acids 30-212 of SEQ ID NO:2. 31. The method of claim 30, wherein said agent is a chimera according to (a) or a derivative according to (c) thereof, or a salt of said chimera or derivative. 32. The method of claim 28, wherein said IL-6 moiety comprises amino acids 30-212 of SEQ ID NO:2. 33. The method of claim 32, wherein said agent is a chimera according to (a) or a derivative according to (c) thereof, or a salt of said chimera or derivative. 34. The method of claim 1, wherein the CIPN is induced by a chemotherapeutic agent that is a vinca alkaloid. 35. The method of claim 1, wherein said chimeric agent comprises, as said IL-6 moiety, amino acids 29-212 of SEQ ID NO:2. 36. The method of claim 1, wherein said chimeric agent comprises, as said soluble IL6R moiety, amino acids 20-356 of SEQ ID NO:1. 37. The method of claim 35, wherein said chimeric agent comprises, as said soluble IL6R moiety, amino acids 20-356 of SEQ ID NO:1. 38. The method of claim 37, wherein said soluble IL6R moiety and said IL6 moiety are (aa) fused directly to one another, or (bb) connected by a linker amino acid or a linker peptide consisting of not more than 30 amino acids. 39. The method of claim 1 wherein the soluble IL6R moiety precedes the IL6 moiety. 40. The method of claim 38 wherein the soluble IL6R moiety precedes the IL6 moiety. 41. The method of claim 1 wherein the chimera of (a) is SEQ ID NO:3. 42. The method of claim 41 wherein the mutein of (b) is at least 90% identical to the chimera of (a). 43. A method for increasing the dose of a chemotherapeutic agent comprising (1) treating and/or inhibiting CIPN by the method of claim 1, and (2) administering to said patient a dose of a chemotherapeutic agent that is increased relative to a dose of that chemotherapeutic agent given the same patient prior to administration of said chimeric agent, wherein said chemotherapeutic agent is not streptozotocin. 44. In a method of chemotherapy that comprises administration of an amount of a chemotherapeutic agent to a patient in need thereof, the improvement comprising inhibiting or treating peripheral neuropathy inducible or induced by said chemotherapeutic agent by the method of claim 1, whereby the amount of said chemotherapeutic agent administered to said patient is higher than the amount that could be given to said patient without inducing peripheral neuropathy in the absence of said chimeric agent, wherein the chemotherapeutic agent is not streptozotocin. 45. The method of claim 44 wherein the chimeric agent is first administered prior to commencement of chemotherapy. 46. The method of claim 44 wherein the chimeric agent is administered at least once with or after commencement of chemotherapy. 47. The method of claim 1 wherein the chimeric agent is first administered prior to commencement of chemotherapy in a patient in need of chemotherapy, and such administration results in inhibition of chemotherapy-induced peripheral neuropathy in said patient after commencement of chemotherapy. 48. The method of claim 1 wherein the total number of insertions and deletions according to (b)(ii)(b') is under 10 amino acids. 49. The method of claim 23 wherein at the time of administration of the chimeric agent, the patient is not suffering from diabetes. 50. The method of claim 49 wherein the soluble IL6R moiety precedes the IL6 moiety. 51. The method of claim 50 wherein the mutein of (b) is at least 90% identical to a chimera of (a). 52. The method of claim 51 wherein said mutein of (b) comprises an amino acid sequence that differs from a chimera of (a) solely by one or more amino acid substitutions. 53. The method of claim 52, wherein the differences between said fragment of human IL-6 and mature human IL-6 consist solely of deletion of one or more residues preceding the first alpha helix of mature human IL-6. 54. The method of claim 53, wherein said chimeric agent comprises, as said soluble IL6R moiety, amino acids 20-356 of SEQ ID NO:1. 55. The method of claim 52, wherein said chimeric agent comprises, as said IL-6 moiety, amino acids 29-212 of SEQ ID NO:2, and as said soluble IL6R moiety, amino acids 20-356 of SEQ ID NO:1. 56. The method of claim 55, wherein said soluble IL6R moiety and said IL6 moiety are (i) fused directly to one another, or (ii) connected by a linker amino acid or a linker peptide consisting of not more than 30 amino acids. 57. The method of claim 56 wherein the chimeric agent is SEQ ID NO:3, or a derivative according to (c) thereof, or a salt of SEQ ID NO:3 or said derivative. 58. The method of claim 57, wherein said chimeric agent is SEQ ID NO:3 or a salt thereof. 59. The method of claim 58 wherein the chimeric agent is administered to the patient with or after administration of a chemotherapeutic agent comprising a vinca alkaloid. 60. The method of claim 58 wherein the chimeric agent is administered to the patient with or after administration of a chemotherapeutic agent comprising vincristine. 61. The method of claim 38 wherein, if (bb) applies, the linker amino acid or linker peptide is 1-3 amino acids, or is a linker peptide selected from the group consisting of EFGAGLVLGGQFM (SEQ ID NO: 6), GGGGDPGGGGGGPG (SEQ ID NO:7), RGGGGSGGGGSVE (SEQ ID NO:8), GGGGSGGGGSGGGGS (SEQ ID NO:9), GGGGSGGGGS (amino acids 1-10 of SEQ ID NO:9), GGGGS (amino acids 1-5 of SEQ ID NO:9), and GGGG (amino acids 1-4 of SEQ ID NO:9).

Details for Patent 8,394,367

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Recordati Rare Diseases, Inc.	ELSPAR	asparaginase	For Injection	101063	01/10/1978		2024-04-29