IP Library Granted Patent US 10,716,859
Granted Patent B2
US 10,716,859 · App. 15/147,114 · Granted Jul 21, 2020

Excipients for stabilising viral particles, polypeptides or biological material

Inventors: Jeffrey Drew (London, GB); David Thomas Woodward (London, GB); John Bainbridge (London, GB); Amanda Corteyn (London, GB)
Assignee: Stabilitech Biopharma Ltd
A61K47/20A61J1/06A61J1/10A61K9/0019A61K9/08A61K39/12A61K39/145A61K39/235A61K39/285A61K41/10A61K47/183A61K47/186A61K47/26A61K47/34C07K16/241C12N7/00A61K2039/525A61K2039/5254C07K2317/55C07K2317/76C12N2710/10334C12N2710/10351C12N2710/24134C12N2710/24151C12N2760/16134C12N2760/16151
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Quick Facts
Patent No.
US 10,716,859
App. No.
15/147,114
Granted
Jul 21, 2020
Kind
B2
Abstract

A sterile pharmaceutically acceptable aqueous solution, which solution is provided in a sealed container and comprises: a pharmaceutically acceptable aqueous solvent; viral particles or a physiologically active polypeptide; an excipient selected from a polyethyleneimine; a compound of formula (I) or a physiologically acceptable salt or ester thereof; or a compound of formula (II) or a physiologically acceptable salt or ester thereof; and optionally, one or more sugars.

Claims (25)

1. A method for the preparation of a ready-to-use, storage-stable aqueous solution which is provided in a sealed container and which contains live viral particles, which method comprises:

(a) providing a solution comprising:

water or physiological saline, which is optionally buffered with a physiologically acceptable buffer;

live viral particles from Adenoviridae, Orthomyxoviridae, Paramyxoviridae, Parvoviridae, Picornaviridae, Poxviridae, Flaviviridae or Herpesviridae;

an excipient which is an N,N-di(C 1-6 alkyl)-glycine or N,N,N-tri(C 1-6 alkyl)-glycine, or a physiologically acceptable salt or ester thereof;

a sulfone compound of formula (IIC):

wherein R a and R b independently represent C 1-6 alkyl; and

optionally one or more sugars; and

(b) sealing the aqueous solution of step (a) in a container, thereby preparing said ready-to-use, storage stable aqueous solution containing live viral particles.

2. The method according to claim 1 , in which the viral particles are from an adenovirus, vaccinia virus, influenza virus or measles virus.

3. The method according to claim 1 , in which the excipient is N,N-dimethylglycine or N,N,N-trimethylglycine, or a physiologically acceptable salt or ester thereof.

4. The method according to claim 3 , in which the excipient is N,N-dimethylglycine or a physiologically acceptable salt or ester thereof.

5. The method according to claim 1 , in which the solution comprises sucrose or mannitol.

6. The method according to claim 5 , in which the solution comprises sucrose and raffinose.

7. The method according to claim 1 , in which the sulfone compound of formula (IIC) is methylsulfonylmethane.

8. The method according to claim 1 , in which the solution is isotonic.

9. The method according to claim 1 , in which the solution is provided in a sealed container under nitrogen.

10. The method according to claim 1 , in which the sealed contained is a sealed vial, ampoule, syringe, cartridge, flexible bag or glass bottle.

11. The method according to claim 1 , in which the solution is passed through a sterilising filter in step (a).

12. A ready-to-use, storage-stable aqueous solution containing live viral particles from Adenoviridae, Orthomyxoviridae, Paramyxoviridae, Parvoviridae, Picornaviridae, Poxviridae, Flaviviridae or Herpesviridae which is provided in a sealed container, said live viral particle containing aqueous solution being obtainable by a method as defined in claim 1 .

13. The aqueous solution according to claim 12 , in which the solution of the method comprises sucrose or mannitol.

14. The aqueous solution according to claim 12 , in which the solution of the method comprises a sulfone of formula (IIC) which is methylsulfonylmethane.

15. The method according to claim 1 , in which the solution comprises sucrose.

16. The method according to claim 1 , in which the solution comprises mannitol.

17. The method according to claim 1 , in which the solution comprises sucrose and mannitol.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2021
From: STABILITECH BIOPHARMA LTD
To: IOSBIO LTD
Reel/Frame 056065/0883 →
CHANGE OF NAME Recorded Jun 19, 2018
From: STABILITECH LTD.
To: STABILITECH BIOPHARMA LTD
Reel/Frame 046129/0440 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 20, 2016
From: DREW, JEFFREY; WOODWARD, DAVID THOMAS; BAINBRIDGE, JOHN; CORTEYN, AMANDA
To: STABILITECH LTD.
Reel/Frame 038962/0291 →
Priority Claims (3)
GB 1005517.6 · Mar 31, 2010 · national
GB 1005521.8 · Mar 31, 2010 · national
GB 1017648.5 · Oct 19, 2010 · national
Continuity (2)
Continuation 13637913
Related Publication 20160317665A1 · Nov 3, 2016