IP Library Granted Patent US 10,660,964
Granted Patent B2
US 10,660,964 · App. 16/164,926 · Granted May 26, 2020

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

Inventor: Rudolf Stefan Widmann (Purkersdorf, AT)
Assignee: AOP Orphan Pharmaceuticals AG
A61K47/40A61K9/0019A61K31/24A61K31/5377A61K31/724A61K47/6951B82Y5/00
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Quick Facts
Patent No.
US 10,660,964
App. No.
16/164,926
Granted
May 26, 2020
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 (11)

1. A pharmaceutical composition comprising:

a) landiolol or a pharmaceutically acceptable salt thereof at a concentration from 0.005 to 0.5% (w/v);

b) water; and

c) 2-hydroxypropyl-β-cyclodextrin at a concentration from 0.5 to 7% (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 0.5 to 5% (w/v).

5. The pharmaceutical composition of claim 1 , wherein the concentration of landiolol or the pharmaceutically acceptable salt thereof is 0.25%.

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

7. The pharmaceutical composition of claim 6 , wherein the composition has an osmolarity of 280 mosmol/l to 300 mosmol/l.

8. The pharmaceutical composition of claim 1 , wherein the composition is present in the form of a sales unit selected from the group consisting of: a 1 ml solution containing 5-20 mg landiolol or a pharmaceutically acceptable salt thereof, a 2 ml solution containing 5-100 mg landiolol or a pharmaceutically acceptable salt thereof, a 5 ml solution containing 10-500 mg landiolol or a pharmaceutically acceptable salt thereof, a 10 ml solution containing 10-5000 mg landiolol or a pharmaceutically acceptable salt thereof, a 25 ml solution containing 25-2500 mg landiolol or a pharmaceutically acceptable salt thereof, a 50 ml solution containing 50-5000 mg landiolol or a pharmaceutically acceptable salt thereof, a 100 ml solution containing 50-5000 mg landiolol or a pharmaceutically acceptable salt thereof, and a 250 ml solution containing 50-5000 mg landiolol or a pharmaceutically acceptable salt thereof.

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 Oct 23, 2018
From: WIDMANN, RUDOLF STEFAN
To: AOP ORPHAN PHARMACEUTICALS AG
Reel/Frame 047281/0794 →
Priority Claims (1)
AT 2107/2007 · Dec 21, 2007 · national
Continuity (3)
Continuation 15248845 · Aug 26, 2016
Continuation 12809927
Related Publication 20190046646A1 · Feb 14, 2019