Granted Patent B2

US 8,875,704 · App. 14/274,271 · Granted Nov 4, 2014

Abstract

Claims (44)

1. A nasal delivery device for delivering g powdered sumatriptan substance to a nasal cavity of a human subject, the delivery device comprising:

a nosepiece for fitting to the nasal cavity of the subject, and

a capsule-containing member which contains a capsule, the capsule containing the powdered sumatriptan substance to be delivered to the nasal cavity of the subject,

wherein the capsule-containing member includes a flow passage in which the capsule is disposed to be rotatable therewithin when an air flow is delivered therethrough, the flow passage including an inlet and an outlet which is in fluid communication with the nosepiece,

wherein the device is configured such that, when the nosepiece is fitted to the nasal cavity of the subject, oral exhalation by the subject through the nosepiece acts to close the velum of the subject and drive an air flow through the nasal cavity, with the air flow passing into one nasal passage and out the other nasal passage, thereby achieving a bi-directional air flow, and

wherein the powdered sumatriptan substance has a particle size distribution of 10% less than about 20 μm, 50% less than about 50 μm and 90% less than about 150 μm.

2. The delivery device of claim 1 , wherein the inlet of the flow passage includes an inlet aperture which provides a flow restriction to an air flow as delivered therethrough.

3. The delivery device of claim 2 , wherein the inlet aperture provides a seat for a lower end of the capsule prior to delivery of an air flow through the flow passage.

4. The delivery device of claim 1 , wherein the flow passage is an elongate flow passage and the capsule is oriented axially therealong.

5. The delivery device of claim 1 , wherein the delivery device is a replaceable nosepiece unit.

6. The delivery device of claim 1 , wherein the powdered sumatriptan substance comprises a sumatriptan base or sumatriptan succinate.

7. The delivery device of claim 1 , wherein the powdered sumatriptan substance contains only sumatriptan succinate and no introduced excipients or adjuvants.

8. The delivery device of claim 7 , wherein the capsule contains 10 mg of sumatriptan succinate powder.

9. The delivery device of claim 1 , wherein the powdered sumatriptan substance has a particle size distribution of 10% less than about 10 μm, 50% less than about 30 μm and 90% less than about 90 μm.

10. A method of treating headache in a human subject, comprising:

fitting a housing and a mouthpiece unit to a first delivery device of claim 1 ;

piercing the capsule in the first delivery device;

fitting the nosepiece of the first delivery device into a first nostril of the subject; and

the subject exhaling through the mouthpiece unit to cause closure of the oropharyngeal velum of the subject and cause the capsule of the first delivery device to be rotated and release the powdered sumatriptan substance from within the capsule of the first delivery device and be entrained in an exhaled air flow.

11. The method of claim 10 , further comprising:

removing the housing and the mouthpiece unit from the first delivery device;

fitting the housing and the mouthpiece unit to a second delivery device of claim 1 ;

piercing the capsule in the second delivery device;

fitting the nosepiece of the second delivery device into a second nostril of the subject; and

the subject exhaling through the mouthpiece unit to cause closure of the oropharyngeal velum of the subject and cause the capsule of the second delivery device to be rotated and release the powdered sumatriptan substance from within the capsule of the second delivery device and be entrained in an exhaled air flow.

12. The method of claim 11 , in the treatment of cluster headaches.

13. The method of claim 11 , in the treatment of migraine.

14. The method of claim 11 , wherein piercing a capsule in the first or second delivery device comprises piercing the capsule at first and second spaced locations along an axial length thereof, and the first and second spaced locations are above a height of the powdered sumatriptan substance as contained by the capsule.

15. A delivery device for delivering a powdered sumatriptan substance to a nasal cavity of a human subject, the delivery device comprising:

a nosepiece for fitting to the nasal cavity of the subject, and

a capsule-containing member which contains a capsule, the capsule containing the powdered sumatriptan substance to be delivered to the nasal cavity of the subject, the powdered sumatriptan substance containing only sumatriptan succinate and no introduced excipients or adjuvants,

wherein the capsule-containing member includes a flow passage in which the capsule is disposed to be rotatable therewithin when an air flow is delivered therethrough, the flow passage including an inlet and an outlet which is in fluid communication with the nosepiece,

wherein the device is configured such that, when the nosepiece is fitted to the nasal cavity of the subject, oral exhalation by the subject through the nosepiece acts to close the velum of the subject and drive an air flow through the nasal cavity, with the air flow passing into one nasal passage and out the other nasal passage, thereby achieving a bi-directional air flow, and

wherein the powdered sumatriptan substance has a particle size distribution of 10% less than about 20 μm, 50% less than about 50 μm and 90% less than about 150 μm.

16. The delivery device of claim 15 , wherein the capsule contains 10 mg of sumatriptan succinate powder.

17. A nasal delivery device for delivering powdered sumatriptan to a nasal cavity of a human subject, the delivery device comprising:

a nosepiece for fitting to the nasal cavity of the subject, and

a capsule-containing member which contains a capsule, the capsule containing the powdered sumatriptan to be delivered to the nasal cavity of the subject,

wherein the capsule-containing member includes a flow passage in which the capsule is disposed to be rotatable therewithin when an air flow is delivered therethrough, the flow passage including an inlet and an outlet which is in fluid communication with the nosepiece, and

wherein the device is configured such that when, the nosepiece is fitted to the nasal cavity of the subject, oral exhalation by the subject through the nosepiece acts to close the velum of the subject and drive an air flow through the nasal cavity, with the air flow passing into one nasal passage and out the other nasal passage, thereby achieving a bi-directional air flow, and

wherein the powdered sumatriptan has a particle size distribution of 10% less than about 20 μm, 50% less than about 50 μm and 90% less than about 150 μm.

18. The delivery device of claim 17 , wherein the powdered sumatriptan comprises a sumatriptan base or sumatriptan succinate.

19. The delivery device of claim 17 , wherein the powdered sumatriptan contains only sumatriptan succinate and no introduced excipients or adjuvants.

20. The delivery device of claim 17 , wherein the capsule contains 10 mg of sumatriptan succinate powder.

Assignments (10)