IP Library Granted Patent US 11,517,624
Granted Patent B2
US 11,517,624 · App. 16/860,336 · Granted Dec 6, 2022

Pharmaceutical composition for the parenteral administration of ultrashort-effective β-adrenoreceptor antagonists

Inventor: Rudolf Stefan Widmann (Purkersdorf, AT)
Assignee: AOP ORPHAN PHARMACEUTICALS GMBH
A61K47/40A61K9/0019A61K31/24A61K31/5377A61K31/724A61K47/6951B82Y5/00
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Quick Facts
Patent No.
US 11,517,624
App. No.
16/860,336
Granted
Dec 6, 2022
Kind
B2
Abstract

The present invention relates to a pharmaceutical composition in the form of a storage-stable solution for the parenteral administration of ultrashort-effective β-adrenoreceptor antagonists, comprising a) an ultrashort-effective β-adrenoreceptor antagonist and/or a pharmaceutically acceptable salt thereof, b) water, and c) a cyclodextrin and/or a functional cyclodextrin derivative. The composition according to the invention has high stability, even without the presence of additional adjuvants.

Claims (17)

1. A pharmaceutical composition comprising:

a) landiolol or a pharmaceutically acceptable salt thereof at a concentration from 0.005 to 2% (w/v);

b) water; and

c) 2-hydroxypropyl-β-cyclodextrin at a concentration from 0.1 to 20% (w/v).

2. The pharmaceutical composition of claim 1 , wherein the pH value of the composition is 3 to 7.5.

3. The pharmaceutical composition of claim 2 , wherein the pH value of the composition is 5 to 7.

4. The pharmaceutical composition of claim 1 , wherein the concentration of 2-hydroxypropyl-β-cyclodextrin is 0.1% to 15% (w/v).

5. The pharmaceutical composition of claim 4 , wherein, the concentration of 2-hydroxypropyl-β-cyclodextrin is 0.25% to 7% (w/v).

6. The pharmaceutical composition of claim 5 , wherein the concentration of 2-hydroxypropyl-β-cyclodextrin is 0.5% to 4%.

7. The pharmaceutical composition of claim 1 , wherein the concentration of the landiolol or pharmaceutically acceptable salt thereof is 0.01% to 1.0% (w/v).

8. The pharmaceutical composition of claim 1 , wherein the composition has an osmolarity of 270 mosmol/l to 310 mosmol/l.

9. The pharmaceutical composition of claim 8 , wherein the composition has an osmolarity of 280 mosmol/l to 300 mosmol/l.

10. The pharmaceutical composition of claim 1 , wherein the composition is present in the form of a sales unit selected from the group consisting of:

1 ml solution containing 5-20 mg landiolol or a salt thereof,

2 ml solution containing 5-40 mg landiolol or a salt thereof.

11. A method of reducing heart beat frequency in a patient comprising administering a composition of claim 1 to a patient, whereby the heart beat frequency in the patient is reduced.

12. The method of claim 11 , wherein the patient has atrial fibrillation, atrial flutter, sinus tachycardia, atrioventricular tachycardia, AV node tachycardia, supraventricular tachycardia, ventricular arrhythmias, perioperative ischaemia, unstable angina pectoris, or acute myocardial infarction.

Assignments (2)
CHANGE OF NAME Recorded Apr 4, 2022
From: AOP ORPHAN PHARMACEUTICALS AG
To: AOP ORPHAN PHARMACEUTICALS GMBH
Reel/Frame 059494/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2020
From: WIDMANN, RUDOLF STEFAN
To: AOP ORPHAN PHARMACEUTICALS AG
Reel/Frame 053643/0740 →
Priority Claims (1)
AT A 2107/2007 · Dec 21, 2007 · national
Continuity (4)
Continuation 16164926 · Oct 19, 2018
Continuation 15248845 · Aug 26, 2016
Continuation 12809927
Related Publication 20200323988A1 · Oct 15, 2020