IP Library Granted Patent US 9,155,694
Granted Patent B2
US 9,155,694 · App. 13/376,021 · Granted Oct 13, 2015

Stabilized composition comprising at least one adrenergic compound

Inventors: Alan J. Baillie (Helensburgh, GB); Kenneth Macdonald (Glasgow, GB); Pamela Porteous (Irvine, GB); Simon Hendry (Wiltshire, GB)
Assignee: ALK AG
A61K9/0019A61K31/137A61K33/04A61K45/06A61K47/02
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Quick Facts
Patent No.
US 9,155,694
App. No.
13/376,021
Granted
Oct 13, 2015
Kind
B2
Abstract

A stabilized composition comprising at least one adrenergic compound and at least one antioxidant selected from the group consisting of a bisulfite, a metabisulfite and a sulfite compound.

Claims (19)

1. A liquid pharmaceutical composition, comprising:

an adrenergic compound as the sole therapeutically active ingredient wherein the adrenergic compound is epinephrine or a physiologically acceptable salt thereof, and

at least one antioxidant selected from the group consisting of a bisulfite, a meta bisulfite and a sulfite compound,

wherein the liquid pharmaceutical composition is a liquid solution, the molar ratio of the adrenergic compound to the at least one antioxidant, measured as sulfite-equivalents, is in the range 0.70-1.30, and the pH of said liquid composition is in the range of 2.0-5.0.

2. The pharmaceutical composition according to claim 1 , wherein the antioxidant is selected from the group consisting of sodium bisulfite and sodium metabisulfite.

3. The pharmaceutical composition according to claim 1 , wherein the antioxidant is sodium metabisulfite.

4. The pharmaceutical composition according to claim 1 , wherein the molar ratio of the adrenergic compound to the at least one antioxidant is in the range of 0.75 to 1.25.

5. The pharmaceutical composition according to claim 1 , having a pH in the range of 2.5-4.5.

6. The pharmaceutical composition according to claim 5 , wherein the pH is in the range of 3.3-3.5.

7. The pharmaceutical composition according to claim 1 , further comprising one or more excipients or additives.

8. The pharmaceutical composition according to claim 1 , comprising 2.0 mg/ml epinephrine acid tartrate, 6.0 mg/ml sodium chloride, and 0.57 mg/ml sodium metabisulfate, and having a pH of 3.4.

9. A method for stabilizing a liquid pharmaceutical composition comprising an adrenergic compound as the sole therapeutically active ingredient, comprising the steps of i) providing a solution of an adrenergic compound, wherein the adrenergic compound is epinephrine or a physiologically acceptable salt thereof, ii) adding at least one antioxidant selected from the group consisting of a bisulfite, a metabisulfite, and a sulfite compound, iii) adjusting the pH thereof to a value in the range 2.0-5.0 optionally by addition of an acid or a base, wherein the liquid pharmaceutical composition is a liquid solution and the molar ratio of the adrenergic compound to the at least one antioxidant, measured as sulfite-equivalents, is in the range 0.70-1.30.

10. A method of stabilizing a liquid pharmaceutical composition which comprises combining at least one antioxidant selected from the group consisting of a bisulfite, a metabisulfite, and a sulfite compound and epinephrine or a physiologically acceptable salt thereof, wherein epinephrine or a physiologically acceptable salt thereof is the sole therapeutically active ingredient, the liquid pharmaceutical composition is a liquid solution, the molar ratio of the epinephrine or a physiologically acceptable salt thereof to the at least one antioxidant, measured as sulfite-equivalents, is in the range 0.70-1.30, and the pH of said liquid composition is in the range of 2.0-5.0.

11. A kit comprising:

i) a liquid pharmaceutical composition comprising an adrenergic compound as the sole therapeutically active ingredient, wherein the adrenergic compound is epinephrine or a physiologically acceptable sale thereof, and at least one antioxidant selected from the group consisting of a bisulfite, a metabisulfite and a sulfite compound, wherein the liquid pharmaceutical composition is a liquid solution, the molar ratio of the adrenergic compound to the at least one antioxidant, measured as sulfite-equivalents, is in the range 0.70-1.30, and the pH of said liquid composition is in the range of 2.0-5.0, and

ii) an administration device.

12. The kit according to claim 11 wherein the administration device is an ampoule or an auto-injector.

13. A method of improving at least one symptom of a medical condition requiring an adrenergic compound in an individual in need thereof, which comprises administering to the individual a liquid pharmaceutical composition comprising an adrenergic compound as the sole therapeutically active ingredient, wherein the adrenergic compound is epinephrine or a physiologically acceptable salt thereof, and at least one antioxidant selected from the group consisting of a bisulfite, a metabisulfite and a sulfite compound, wherein the liquid pharmaceutical composition is a liquid solution, the molar ratio of the adrenergic compound to the at least one antioxidant, measured as sulfite-equivalents, is in the range 0.70-1.30, and the pH of said liquid composition is in the range of 2.0-5.0.

14. A method of treating anaphylaxis in an individual comprising administering to the individual a liquid pharmaceutical composition comprising an adrenergic compound as the sole therapeutically active ingredient, wherein the adrenergic compound is epinephrine or a physiologically acceptable salt thereof, and at least one antioxidant selected from the group consisting of a bisulfite, a metabisulfite and a sulfite compound, wherein the liquid pharmaceutical composition is a liquid solution, the molar ratio of the adrenergic compound to the at least one antioxidant, measured as sulfite-equivalents, is in the range 0.70-1.30, and the pH of said liquid composition is in the range of 2.0-5.0.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2016
From: ALK AG
To: ALK ABELLO A/S
Reel/Frame 038380/0112 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2012
From: BAILLIE, ALAN J.; MACDONALD, KENNETH; PORTEOUS, PAMELA; HENDRY, SIMON
To: ALK AG
Reel/Frame 027583/0683 →
Priority Claims (1)
DK PA200900705 · Jun 4, 2009 · national
Continuity (2)
Provisional Application 61184066 · Jun 4, 2009
Related Publication 20120129944A1 · May 24, 2012