IP Library Granted Patent US 8,399,496
Granted Patent B2
US 8,399,496 · App. 12/229,425 · Granted Mar 19, 2013

Inhalable aztreonam lysinate formulation for treatment and prevention of pulmonary bacterial infections

Inventors: Alan Bruce Montgomery (Seattle, WA); Manfred Keller (München, DE); Frank-Christophe Lintz (Starnberg, DE)
Assignee: Gilead Sciences, Inc.
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Quick Facts
Patent No.
US 8,399,496
App. No.
12/229,425
Granted
Mar 19, 2013
Kind
B2
Abstract

A method and a composition for treatment of pulmonary bacterial infections caused by gram-negative bacteria suitable for treatment of infection caused by Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Pseudomonas aeruginosa, Haemophilus influenzae, Proteus mirabilis, Enterobacter species, Serratia marcescens as well as those caused by Burkholderia cepacia, Stenotrophomonas maltophilia, Alcaligenes xylosoxidans , and multidrug resistant Pseudomonas aeruginosa , using a concentrated formulation of aztreonam lysinate delivered as an aerosol or dry powder formulation.

Claims (24)

1. An inhalable composition comprising astreonam lysinate and a pharmaceutically acceptable diluent.

2. A method for administering by inhalation aztreonam lysinate comprising administering a composition comprising aztreonam lysinate and a pharmaceutically acceptable diluent.

3. The method according to claim 2 , wherein the diluent is saline.

4. The method according to claim 2 , wherein said composition comprises from about 1 to about 250 mg of aztreonam lysinate dissolved in about 1 to about 5 mL of saline solution containing from about 0.1 to about 0.9%, w/v, of sodium chloride.

5. The method according to claim 2 , wherein said composition is delivered by a nebulizer.

6. The method according to claim 5 , wherein said nebulizer is an atomizing jet, ultrasonic, electronic or vibrating porous plate nebulizer.

7. The method according to claim 2 , wherein said composition consists of 75 mg of aztreonam and 47 mg of lysine per 1 mL of saline.

8. A method for improving pulmonary function in a patient with cystic fibrosis, said method comprising administering by inhalation aztreonam lysinate to said patient.

9. The method according to claim 8 , wherein said step of administering comprises administering a composition comprising aztreonam lysinate and a pharmaceutically acceptable diluent.

10. The method according to claim 9 , wherein the diluent is saline.

11. The method according to claim 9 , wherein said composition comprises from about 1 to about 250 mg of aztreonam lysinate dissolved in about 1 to about 5 mL of saline solution containing from about 0.1 to about 0.9%, w/v, of sodium chloride.

12. The method according to claim 9 , wherein said composition is delivered by a nebulizer.

13. The method according to claim 12 , wherein said nebulizer is an atomizing jet, ultrasonic, electronic or vibrating porous plate nebulizer.

14. The method according to claim 11 , wherein said composition consists of 75 mg of aztreonam and 47 mg of lysine per 1 mL of saline.

15. A method for treating an infection caused by gram-negative bacteria in a patient with cystic fibrosis, said method comprising administering by inhalation an aztreonam lysinate composition to said patient, wherein said composition comprises from about 1 to about 250 mg of aztreonam lysinate dissolved in about 1 to about 5 mL of saline solution containing from about 0.1 to about 0.9%. w/v, of sodium chloride.

16. The method according to claim 15 , wherein said composition consists of sodium chloride composition consists of 75 mg of aztreonam and 47 mg of lysine per 1 mL of saline.

17. A method according to claim 15 , wherein said composition is delivered by a nebulizer.

18. The method according to claim 17 , wherein said nebulizer is an atomizing jet, ultrasonic, electronic or vibrating porous plate nebulizer.

19. A method for treating an infection caused by gram-negative bacteria in a patient with bronchiectasis, said method comprising administering by inhalation aztreonam lysinate to said patient

20. The method according to claim 19 , wherein said step of administering comprises administering a composition comprising aztreonam lysinate and a pharmaceutically acceptable diluent.

21. The method according to claim 20 , wherein said composition comprises from about 1 to about 250 mg of aztreonam lysinate dissolved in about 1 to about 5 mL of saline solution containing from about 0.1 to about 0.9%, w/v, of sodium chloride.

22. The method according to claim 21 , wherein said composition is delivered by a nebulizer.

23. The method according to claim 22 , wherein said nebulizer is an atomizing jet, ultrasonic, electronic, or vibrating porous plate nebulizer.

24. The method according to claim 21 , wherein said composition consists of 75 mg of aztreonam and 47 mg of lysine per 1 mL of saline.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2010
From: KELLER, MANFRED; LINTZ, FRANK-CHRISTOPHE
To: CORUS PHARMA, INC.
Reel/Frame 024147/0953 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2010
From: MONTGOMERY, ALAN BRUCE
To: CORUS PHARMA, INC.
Reel/Frame 024147/0979 →
MERGER Recorded Mar 26, 2010
From: CORUS PHARMA, INC.
To: GILEAD SCIENCES, INC.
Reel/Frame 024148/0007 →
Continuity (5)
Continuation 11732234 · Apr 2, 2007
Division 10613639 · Jul 3, 2003
Continuation In Part 10027113 · Dec 20, 2001
Provisional Application 60258423 · Dec 27, 2000
Related Publication 20090028801A1 · Jan 29, 2009