IP Library Granted Patent US 8,158,651
Granted Patent B2
US 8,158,651 · App. 11/656,970 · Granted Apr 17, 2012

Fentanyl composition for nasal administration

Assignee: Nycomed Danmark Aps
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Quick Facts
Patent No.
US 8,158,651
App. No.
11/656,970
Granted
Apr 17, 2012
Kind
B2
Abstract

The treatment of acute pain with a sufficient dosage by intranasal administration of fentanyl results in a time to onset of action comparable to intravenous administration and a significantly faster onset of action than nasal titration of fentanyl. The nasal administration of a sufficient amount of fentanyl to obtain pain relief has lower maximum plasma concentrations comparable to intravenous administration and results in lower rates of adverse events like respiratory depression, nausea and vomiting. Compositions fur use in the method are also disclosed.

Claims (12)

1. A device in combination with a liquid pharmaceutical composition comprising a fentanyl salt in a solvent comprising about 95-100% water at a concentration range equivalent to 0.5-20 mg/ml of fentanyl, said device comprising means for intranasal spray delivery of said composition in a dosage unit equivalent to 70 to 500 μg of fentanyl.

2. The device according to claim 1 , wherein the concentration range is equivalent to 0.6-15 mg/ml fentanyl.

3. The device according to claim 1 , wherein the concentration range is equivalent to 0.75-10 mg/ml fentanyl.

4. The device according to claim 1 , wherein the concentration is equivalent to 1 mg/ml.

5. The device according to claim 1 , wherein the concentration is equivalent to 2 mg/ml.

6. The device according to claim 1 , wherein said fentanyl salt is fentanyl citrate.

7. The device according to claim 2 , wherein said fentanyl salt is fentanyl citrate.

8. The device according to claim 3 , wherein said fentanyl salt is fentanyl citrate.

9. The device according to claim 4 , wherein said fentanyl salt is fentanyl citrate.

10. The device according to claim 5 , wherein said fentanyl salt is fentanyl citrate.

11. The device according to claim 1 , wherein the solvent is isotonic saline.

12. The device according to claim 1 , wherein the solvent further comprises polyethylene glycol.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2024
From: TAKEDA PHARMA A/S
To: ISTITUTO GENTILI S.R.L.
Reel/Frame 067344/0392 →
CHANGE OF ADDRESS Recorded Mar 2, 2022
From: TAKEDA PHARMA A/S
To: TAKEDA PHARMA A/S
Reel/Frame 059289/0393 →
NOTICE OF CHANGE OF ASSIGNEE'S ADDRESS Recorded Jan 21, 2015
From: TAKEDA PHARMA A/S
To: TAKEDA PHARMA A/S
Reel/Frame 034783/0357 →
CHANGE OF NAME Recorded Aug 14, 2013
From: NYCOMED DANMARK APS
To: TAKEDA PHARMA A/S
Reel/Frame 031014/0072 →
CHANGE OF NAME Recorded Apr 2, 2013
From: NYCOMED DANMARK APS
To: TAKEDA PHARMA A/S
Reel/Frame 030131/0668 →
CHANGE OF NAME Recorded May 7, 2009
From: NYCOMED DANMARK A/S
To: NYCOMED DANMARK APS
Reel/Frame 022660/0103 →
Priority Claims (1)
DK 2000 01154 · Jul 31, 2000 · national
Continuity (2)
Division 10343449
Related Publication 20070134164A1 · Jun 14, 2007