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Glycopegylated Erythropoietin

a technology of erythropoietin and erythropoietin, which is applied in the field of glycopegylated erythropoietin, can solve the problems of microheterogeneity, protein glycosylation, and numerous problems, and achieve the effect of improving pharmacokinetic properties and cost-effectiveness

Inactive Publication Date: 2007-11-01
NOVO NORDISK AS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0016] It has now been discovered that the controlled modification of erythropoietin (EPO) with one or more poly(ethylene glycol) moieties affords novel EPO derivatives with improved pharmacokinetic properties. Furthermore, cost effective methods for reliable production of the modified EPO peptides of the invention have been discovered and developed.

Problems solved by technology

Unfortunately, one frustrating, and well known aspect of protein glycosylation is the phenomenon of microheterogeneity.
The problem of microheterogeneity thus poses numerous problems for the large industrial scale production of therapeutic glycoproteins.
Further complications arise from the fact that different production batches may vary with respect to the percentage of the desired glycoform comprising the batch of glycoprotein therapeutic.
Thus, large, not always predictable portions of each preparation may be have to be discarded, so that ultimately the final yield of a desired glycoform can be low.
Overall, the problem of microheterogeneity means that therapeutic glycopeptides produced by mammalian cell culture require higher production costs, which ultimately translate to higher health care costs than might be necessary if a more efficient method for making longer lasting, more effective glycoprotein therapeutics was available.
Of course, random addition of PEG molecules has its drawbacks, including a lack of homogeneity of the final product, and the possibility for reduction in the biological or enzymatic activity of the peptide.
Although commercially available forms of EPO are in use today, these peptides are less than maximally effective due factors including microheterogeneity of the glycoprotein product which increases production costs, poor pharmacokinetics of the resulting isolated glycoprotein product, or a combination of the two.

Method used

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Examples

Experimental program
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Effect test

example 1

Preparation of UDP-GalNAc-6′-CHO

[0371] UDP-GalNAc (200 mg, 0.30 mmoles) was dissolved in a 1 mM CuSO4 solution (20 mL) and a 25 mM NaH2PO4 solution (pH 6.0; 20 mL). Galactose oxidase (240 U; 240 μL) and catalase (13000 U; 130 μL) were then added, the reaction system equipped with a balloon filled with oxygen and stirred at room temperature for seven days. The reaction mixture was then filtered (spin cartridge; MWCO 5K) and the filtrate (˜40 mL) was stored at 4° C. until required. TLC (silica; EtOH / water (7 / 2); Rf=0.77; visualized with anisaldehyde stain).

example 2

Preparation of UDP-GalNAc-6′-NH2):

[0372] Ammonium acetate (15 mg, 0.194 mmoles) and NaBH3CN (1M THF solution; 0.17 mL, 0.17 mmoles) were added to the UDP-GalNAc-6′-CHO solution from above (2 mL or ˜20 mg) at 0° C. and allowed to warm to room temperature overnight. The reaction was filtered through a G-10 column with water and the product collected. The appropriate fractions were freeze-dried and stored frozen. TLC (silica; ethanol / water (7 / 2); Rf=0.72; visualized with ninhydrin reagent).

example 3

Preparation of UDP-GalNAc-6-NHCO(CH2)2—O-PEG-OMe (1 KDa).

[0373] The galactosaminyl-1-phosphate-2-NHCO(CH2)2—O-PEG-OMe (1 KDa) (58 mg, 0.045 mmoles) was dissolved in DMF (6 mL) and pyridine (1.2 mL). UMP-morpholidate (60 mg, 0.15 mmoles) was then added and the resulting mixture stirred at 70° C. for 48 h. The solvent was removed by bubbling nitrogen through the reaction mixture and the residue purified by reversed phase chromatography (C-18 silica, step gradient between 10 to 80%, methanol / water). The desired fractions were collected and dried at reduced pressure to yield 50 mg (70%) of a white solid. TLC (silica, propanol / H2O / NH4OH, (30 / 20 / 2), Rf=0.54). MS (MALDI): Observed, 1485, 1529, 1618, 1706.

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Abstract

The present invention provides conjugates between erythropoietin and PEG moieties. The conjugates are linked via an intact glycosyl linking group interposed between and covalently attached to the peptide and the modifying group. The conjugates are formed from glycosylated peptides by the action of a glycosyltransferase. The glycosyltransferase ligates a modified sugar moiety onto a glycosyl residue on the peptide. Also provided are methods for preparing the conjugates, methods for treating various disease conditions with the conjugates, and pharmaceutical formulations including the conjugates.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS [0001] The present application claims priority to U.S. Provisional Patent Application No. 60 / 524,989, filed Nov. 24, 2003; U.S. Provisional Patent Application No. 60 / 555,504, filed Mar. 22, 2004; U.S. Provisional Patent Application No. 60 / 590,573, filed Jul. 23, 2004; U.S. Provisional Patent Application No. 60 / 592,744, filed Jul. 29, 2004; U.S. Provisional Patent Application No. 60 / 614,518, filed Sep. 29, 2004; and U.S. Provisional Patent Application No. 60 / 623,387 each of which is incorporated herein by reference in their entirety for all purposes.BACKGROUND OF THE INVENTION [0002] Erythropoietin (EPO) is a cytokine produced by the kidney and liver which acts on hematopoietic stem cells to stimulate the production of red blood cells. The protein exists in two forms: one being a 165 amino acid peptide, and the other is a 166 amino acid peptide. The 166 amino acid peptide has the same sequence as the 165 amino acid peptide except that the 166 ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/16A61P7/00C07K1/00A61KA61K38/00A61K38/18C07K7/00C07K14/505
CPCA61K38/00C07K14/505C07H19/10A61K47/48215A61K47/60A61P17/02A61P7/00A61P7/06C07K14/435
Inventor DEFREES, SHAWNBAYER, ROBERT J.ZOPF, DAVID A.
Owner NOVO NORDISK AS
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