Intranasal spray device containing pharmaceutical composition
View Patent ↗An intranasal spray device contains a composition for the intranasal delivery of fentanyl or a pharmaceutically acceptable salt thereof to an animal includes an aqueous solution of fentanyl or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable additive selected from (i) a pectin and (ii) a poloxamer and chitosan or a salt or derivative thereof; provided that when the composition comprises a pectin it is substantially free of divalent metal ions; and which, in comparison to a simple aqueous solution of fentanyl administered intranasally at the same dose, provides a peak plasma concentration of fentanyl (C max ) that is from 10 to 80% of that achieved using a simple aqueous solution of fentanyl administered intranasally at an identical fentanyl dose. A method for treating or managing pain by intranasally administering the composition is also disclosed.
1. An intranasal spray device containing a pharmaceutical composition comprising an aqueous solution of
from 0.05 mg/ml to 30 mg/ml of fentanyl or a pharmaceutically acceptable salt thereof (expressed as fentanyl base) and
a pectin having a degree of esterification (DE value) of 7% to 30%, provided that the composition is substantially free of divalent metal ions,
wherein the composition when administered intranasally to a subject in a single dosage regimen provides a practical dose volume which
provides a peak plasma concentration of fentanyl (C max ) that is from 10% to 80% of that achieved using a simple aqueous solution of fentanyl administered intranasally at an identical fentanyl dose; and
provides a time to achieve peak plasma concentration (T max ) of fentanyl in the subject's plasma of 5 minutes to 30 minutes,
wherein the single dosage regimen is effective to treat or manage pain.
2. An intranasal spray device according to claim 1 , which is a unit dose device.
3. An intranasal spray device according to claim 2 , comprising a bottle, a pump and an actuator.
4. An intranasal spray device according to claim 1 , which is a multiple dose device.
5. An intranasal spray device according to claim 4 , comprising a bottle, a pump and an actuator.
6. An intranasal spray device according to claim 1 , comprising means for delivering from 0.01 ml to 0.15 ml of the pharmaceutical composition in a single actuation.
7. An intranasal spray device according to claim 1 , comprising means for intranasal spray delivery of the pharmaceutical composition in a dosage unit of 10 μg to 5000 pig of fentanyl (expressed as fentanyl base).
8. An intranasal spray device according to claim 7 , comprising means for intranasal spray delivery of a dosage unit of 10 μg to 3000 μg of fentanyl (expressed as fentanyl base).
9. An intranasal spray device according to claim 8 , wherein the pectin has a DE value of from 10% to 25%.
10. An intranasal spray device according to claim 8 , wherein the pectin has a DE value of from 15% to 25%.
11. An intranasal spray device according to claim 1 , wherein the composition comprises a pharmaceutically acceptable salt of fentanyl.
12. An intranasal spray device according to claim 11 , wherein the pharmaceutically acceptable salt of fentanyl is fentanyl citrate.
13. An intranasal spray device according to claim 1 , wherein the composition has a concentration of pectin from 5 mg/ml to 25 mg/ml of the composition.
14. An intranasal spray device according to claim 1 , wherein the composition is at least 99% free of divalent metal ions.
15. An intranasal spray device according to claim 1 , wherein the composition has an osmolality of from 0.2 osmol/kg to 0.8 osmol/kg.
16. An intranasal spray device according to claim 15 , wherein the composition has an osmolality of from 0.2 osmol/kg to 0.4 osmol/kg.
17. An intranasal spray device according to claim 16 , wherein the composition has an osmolality of from 0.25 osmol/kg to 0.35 osmol/kg.
18. An intranasal spray device according to claim 15 , wherein the pharmaceutical composition comprises a non-metal ion osmolality adjusting agent.
19. An intranasal spray device according to claim 18 , wherein the non-metal ion osmolality adjusting agent is selected from one or more in the group consisting of mannitol, sorbitol, dextrose, sucrose and trehalose.
20. An intranasal spray device according to claim 1 , wherein the composition has a pH of from 3 to 6.
21. An intranasal spray device according to claim 20 , wherein the composition has a pH of from 3.2 to 5.5.
22. An intranasal spray device according to claim 21 , wherein the composition has a pH of from 3.4 to 5.0.
23. An intranasal spray device according to claim 1 , wherein the composition comprises from 0.1 mg/ml to 20 mg/ml of fentanyl or a pharmaceutically acceptable salt thereof (expressed as fentanyl base).
24. An intranasal spray device according to claim 23 , wherein the composition comprises from 0.2 mg/ml to 16 mg/ml of fentanyl or a pharmaceutically acceptable salt thereof (expressed as fentanyl base).
25. An intranasal spray device containing a pharmaceutical composition comprising an aqueous solution of 0.1 mg/ml to 20 mg/ml (expressed as fentanyl base) of fentanyl or a pharmaceutically acceptable salt thereof and 5 mg/ml to 25 mg/ml of a pectin having a DE value of 10% to 25%; the composition having a pH of 3.4 to 5.0 and an osmolality of 0.20 osmol/mg to 0.40 osmol/kg and being substantially free of divalent metal ions,
wherein the composition when administered intranasally to a subject in a single dosage regimen provides a practical dose volume which provides a peak plasma concentration of fentanyl (C max ) that is from 10% to 80% of that achieved using a simple aqueous solution of fentanyl administered intranasally at an identical fentanyl dose; and
wherein the intranasal administration of the composition provides a time to achieve peak plasma concentration (T max ) of fentanyl in the subject's plasma of 5 minutes to 30 minutes, and
wherein the single dosage regimen is effective to treat or manage pain.
26. An intranasal spray device according to claim 25 , wherein the composition comprises from 0.2 mg/ml to 16 mg/ml of fentanyl or a pharmaceutically acceptable salt thereof (expressed as fentanyl base).