IP Library Granted Patent US 8,715,623
Granted Patent B2
US 8,715,623 · App. 11/981,986 · Granted May 6, 2014

Pulmonary delivery of aminoglycoside

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Quick Facts
Patent No.
US 8,715,623
App. No.
11/981,986
Granted
May 6, 2014
Kind
B2
Abstract

A dispersible powder composition comprises aminoglycoside for delivery to the lungs. The composition is effective to provide a therapeutically effective therapy via administration of less than 6 respirable unit doses by inhalation, wherein each unit dose comprises a volume of 0.30 to 0.95 mL.

Claims (33)

1. A dispersible powder composition comprising particles comprising an aminoglycoside and a phospholipid for delivery to the lungs by inhalation, wherein the particles have a geometric diameter of less than 5 microns, the composition being effective to provide a therapeutically effective therapy via administration of less than 6 respirable unit doses, and wherein each respirable unit dose comprises a volume of 0.30 to 0.95 ml.

2. A composition according to claim 1 wherein the composition comprises from about 50% to about 99% by weight aminoglycoside.

3. A composition according to claim 2 wherein the particles further comprise calcium chloride.

4. A composition according to claim 1 wherein the respirable unit dose is provided in a capsule, the capsule comprising hydroxypropylmethylcellulose.

5. A composition according to claim 1 wherein the particles have a bulk density of between 0.08 and 0.20 g/cm 3 .

6. A composition according to claim 1 wherein each respirable unit dose comprises a fill mass of between 25 and 50 mg, and said fill mass comprises between about 14-35 mg of aminoglycoside or salt thereof.

7. A composition according to claim 1 wherein the particles have a mass median aerodynamic diameter less than 5 microns.

8. A composition according to claim 1 having a pH of between 7 and 10.

9. A composition according to claim 1 wherein each respirable unit dose comprises a volume equivalent to a size #00 capsule or smaller capsule size.

10. A composition according to claim 1 wherein each respirable unit dose comprises a volume equivalent to a size #2 capsule or smaller capsule size.

11. A composition according to claim 1 wherein the aminoglycoside comprises tobramycin or salt thereof.

12. A composition according to claim 1 comprising calcium.

13. A composition according to claim 1 wherein the particles are spray dried particles.

14. A composition according to claim 1 wherein each respirable unit dose comprises 10-60 mg of aminoglycoside or salt thereof.

15. A composition according to claim 1 wherein the aminoglycoside comprises one or more of gentamicin, netilmicin, paramecin, tobramycin, amikacin, kanamycin, neomycin, and streptomycin.

16. A composition according to claim 1 wherein the particles have a moisture content of less than 15% by weight.

17. A composition according to claim 1 wherein the composition provides therapeutically effective therapy via administration of less than 5 respirable unit doses comprising the composition.

18. A method for administering a composition, the method comprising administering by inhalation less than 6 respirable unit doses of the composition according to claim 1 to provide at least 27.6 mg of aminoglycoside to the lungs.

19. A method for treating cystic fibrosis, the method comprising administering a pharmacologically effective amount of aminoglycoside comprising tobramycin to the lungs from a respirable unit dose according to claim 1 .

20. A method for administering aminoglycoside to reduce the potential for development of bacteria in the lungs, the method comprising administering a pharmacologically effective amount of aminoglycoside to the lungs from a respirable unit dose according to claim 1 .

21. A capsule comprising a composition for delivery of aminoglycoside to the lungs by inhalation, the composition including particles comprising phospholipid and aminoglycoside, the aminoglycoside comprising tobramycin, a geometric diameter less than 5 microns, a mass median aerodynamic diameter less than 5 microns, and a bulk density of greater than 0.08 g/cm 3 , wherein the capsule comprises a volume that is equivalent to, or less than, a capsule volume corresponding to a size #2 capsule, and wherein the capsule contains aminoglycoside or salt thereof, in an amount of 10-60 mg, whereby an effective dose of the aminoglycoside can be administered to the lungs using less than 6 capsules.

22. A pulmonary delivery method comprising administering a pharmacologically effective amount of tobramycin to the lungs by providing a composition comprising particles dispersed from less than 6 capsules by an inhalation device, the particles comprising a matrix of phospholipid and; tobramycin or a salt thereof, a bulk density of greater than 0.08 g/cm 3 , and having a pH of 7 or higher, wherein an effective amount of the tobramycin can be administered to the lungs in less than 6 respirable unit doses.

23. A dispersible powder composition comprising particles comprising phospholipid and tobramycin or salt thereof, the particles characterized by a geometric diameter of less than 5 microns, a mass median aerodynamic diameter of less than 5 microns, and a bulk density of between 0.08 g/cm 3 and 0.20 g/cm 3 , wherein the amount of tobramycin or salt thereof in the particles is from about 50% to about 99%, wherein the composition is in the form of a unit dose containing the tobramycin or salt thereof in an amount of 10-60 mg, wherein a therapeutic dose of the tobramycin or salt thereof can be administered to the lungs in less than 6 respirable unit doses, each unit dose comprising a volume of 0.30 mL to 0.95 mL.

24. A respirable unit dose according to claim 23 comprising a volume equivalent to a size #0 capsule or less.

25. A composition according to claim 1 wherein the particles are hollow and porous.

26. A composition according to claim 1 wherein each respirable unit dose comprises an emitted dose greater than 70%.

27. A composition according to claim 1 wherein the particles have a bulk density of less than 0.20 g/cm 3 .

28. A method according to claim 22 wherein the particles comprise tobramycin or salt thereof in a potency of greater than 60%.

29. A method according to claim 22 wherein at least 27.6 mg of the tobramycin or salt thereof can be administered to the lungs in less than 6 respirable doses.

30. A composition according to claim 23 wherein the unit dose comprises a volume of less than 0.68 mL.

31. A composition according to claim 23 wherein the unit dose is contained in a size 2 capsule.

32. A composition according to claim 23 wherein the particles further comprise calcium chloride.

33. A composition according to claim 23 wherein the particles are hollow and porous.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2018
From: NOVARTIS PHARMA AG
To: BGP PRODUCTS OPERATIONS GMBH
Reel/Frame 047152/0017 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2014
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 032351/0866 →
ASSIGNMENT OF PATENT RIGHTS Recorded Jan 7, 2009
From: NEKTAR THERAPEUTICS
To: NOVARTIS PHARMA AG
Reel/Frame 022071/0001 →