Pharmaceutical preparation comprising recombinant HcG

Patent metadata

Field	Value
Publication number	US-9676835-B2
Application number	US-201414283904-A
Country	US
Kind code	B2
Filing date	May 21, 2014
Priority date	Oct 5, 2009
Publication date	Jun 13, 2017
Grant date	Jun 13, 2017

Abstract

The present disclosure describes recombinant human chorionic gonadotropin (hCG) and methods for the production thereof. The recombinant hCG can include α2,3, α2,6, and, optionally, α2,8 sialylation. The recombinant hCG can be produced in a human cell line such as a PER.C6® cell line.

First claim

The invention claimed is:

1. A pharmaceutical composition comprising recombinant human chorionic gonadotropin (hCG), wherein the recombinant hCG in the composition comprises α2,3- and α2,6-sialylation, and wherein the recombinant hCG in the composition is glycosylated and comprises mono- (1S), di- (2S), tri- (3S) and tetra- (4S) sialylated glycan structures.

2. The pharmaceutical composition of claim 1 , wherein the recombinant hCG has a sialic acid content of 15 moles of sialic acid per mole of the recombinant hCG protein.

3. The pharmaceutical composition of claim 1 , wherein the recombinant hCG has a sialic acid content of from 15 to 25 moles of sialic acid per mole of the recombinant hCG protein.

4. The pharmaceutical composition of claim 1 wherein 10% or more of the total sialylation of the recombinant hCG is α2,3-sialylation.

5. The pharmaceutical composition of claim 1 wherein 45% to 80% of the total sialylation of the recombinant hCG is α2,3-sialylation.

6. The pharmaceutical composition of claim 1 wherein 20% to 55% of the total sialylation of the recombinant hCG is α2,6-sialylation.

7. The pharmaceutical composition of claim 1 wherein the recombinant hCG in the composition further comprises α2,8-sialylation.

8. The pharmaceutical composition of claim 1 wherein the recombinant hCG has a sialic acid content of 6% or greater by mass.

9. The pharmaceutical composition of claim 1 wherein the recombinant hCG is produced or expressed in a human cell line.

10. The pharmaceutical composition of claim 9 wherein the cell line is modified using α2,3-sialyltransferase.

11. The pharmaceutical composition of claim 9 wherein the recombinant hCG includes α2,6-linked sialic acids provided by endogenous sialyl transferase activity.

12. The pharmaceutical composition of claim 1 , wherein the relative amounts of mono- (1S), di- (2S), tri- (3S), and tetra- (4S) sialylated glycan structures are in the following ratios of amounts: 0.2-1:35-40:2.5-7:0.5-1, wherein the ratio of amounts is expressed as the ratio of 1S:2S:3S:4S.

13. The pharmaceutical composition of claim 1 wherein 50% or less of the total sialylation of the recombinant hCG is α2,6-sialylation.

14. The pharmaceutical composition of claim 1 wherein 10% or more of the total sialylation of the recombinant hCG is α2,3-sialylation and wherein 50% or less of the total sialylation of the recombinant hCG is α2,6-sialylation.

15. The pharmaceutical composition of claim 1 wherein 10% to 90% of the total sialylation of the recombinant hCG is α2,3-sialylation.

16. The pharmaceutical composition of claim 1 further comprising follicle stimulating hormone (FSH) or luteinizing hormone (LH), or both FSH and LH.

17. The pharmaceutical composition of claim 1 , further comprising a pharmaceutically acceptable carrier.

18. The pharmaceutical composition of claim 17 , wherein the composition is a sterile, injectable isotonic aqueous solution.

19. A method of manufacturing a pharmaceutical composition according to claim 1 comprising producing, in a recombinant human cell line, recombinant hCG that is glycosylated and comprises mono- (1S), di- (2S), tri- (3S) and tetra- (4S) sialylated glycan structures, and wherein the sialylation of the recombinant hCG comprises α2,3- and α2,6-sialylation, and formulating the hCG to produce the pharmaceutical composition.

20. A method of treatment of infertility comprising a step of administering to a subject in need of such treatment a composition according to claim 1 .

Assignees

• Ferring Bv

Inventors

• Cottingham Ian
• Plaksin Daniel
• White Richard Boyd

Classifications

• A61P5/06

  of the anterior pituitary hormones, e.g. TSH, ACTH, FSH, LH, PRL, GH · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P15/08

  for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis · CPC title

• C12P21/005

  Glycopeptides, glycoproteins · CPC title

• C07K14/575 Primary

  Hormones (derived from pro-opiomelanocortin, pro-enkephalin or pro-dynorphin C07K14/665, e.g. corticotropin C07K14/695) · CPC title