IP Library Granted Patent US 9,918,993
Granted Patent B2
US 9,918,993 · App. 15/184,768 · Granted Mar 20, 2018

Pharmaceutical compositions for anesthesiological applications

Inventors: John Berdahl (Sioux Falls, SD); William F. Wiley (Chagrin Falls, OH); Dennis Elias Saadeh (Irvine, CA)
Assignee: IMPRIMIS PHARMACEUTICALS, INC.
A61K31/5517A61K9/0056A61K31/135A61K31/138A61K45/06
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Quick Facts
Patent No.
US 9,918,993
App. No.
15/184,768
Granted
Mar 20, 2018
Kind
B2
Abstract

Pharmaceutical compositions and methods are described, the compositions comprising a benzodiazepine-based compound, a NMDA antagonist, a β-blocker and antiemetic. Methods for fabricating the compositions and using them for anesthesiological applications are also described.

Claims (26)

1. A pharmaceutical composition, comprising:

(a) a therapeutically effective quantity of a first pharmaceutically active compound selected from the group consisting of midazolam, diazepam, lorazepam, flunitrazepam, alprazolam, chlordiazepoxide, clonazepam and clorazepate, and pharmaceutically acceptable salts, hydrates, solvates or N-oxides thereof;

(b) a therapeutically effective quantity of a second pharmaceutically active compound selected from the group consisting of ketamine, dextrorphan, etomidate, methadone, memantine, amantadine, dextromethorphan, and pharmaceutically acceptable salts, hydrates, solvates or N-oxides thereof;

(c) a pharmaceutically suitable binder therefor; and

(d) optionally, a pharmaceutically acceptable excipient,

wherein the pharmaceutical composition is formulated as a solid item adapted for sublingual or buccal administration, the solid item being selected from the group consisting of a troche, a lozenge, a capsule, a pill, a cap and a bolus.

2. The pharmaceutical composition of claim 1 , further comprising a therapeutically effective quantity of a third pharmaceutically active compound selected from the group consisting of β-blockers, antiemetic medicaments, and combinations thereof, or pharmaceutically acceptable salts, hydrates, solvates or N-oxides thereof.

3. The pharmaceutical composition of claim 2 , wherein the β-blocker is selected from the group consisting of metoprolol, propranolol, acebutolol, nadolol, atenolol, betaxolol, esmolol, bisoprolol fumarate, carvedilol, nebivolol, penbutolol, timolol and sotalol.

4. The pharmaceutical composition of claim 2 , wherein the antiemetic medicament is selected from the group consisting of ondansentron, dolasetron, granisetron, palonosetron, promethazine, imenhydrinate, and meclizine.

5. The pharmaceutical composition of claim 2 , further comprising a therapeutically effective quantity of a receptor antagonist to benzodiazepines.

6. The pharmaceutical composition of claim 5 , wherein the receptor antagonist is flumazenil.

7. The pharmaceutical composition of claim 2 , wherein the first pharmaceutically active compound is medazolam, the second pharmaceutically active compound is ketamine and the third pharmaceutically active compound is metoprolol, wherein the medazolam:ketamine:metoprolol ratio is between about 1:2:1 and about 1:10:1 by mass.

8. The pharmaceutical composition of claim 2 , wherein the first pharmaceutically active compound is medazolam, the second pharmaceutically active compound is ketamine and the third pharmaceutically active compound is ondansentron, wherein the medazolam:ketamine:ondansentron ratio is about 3:25:2 by mass.

9. The pharmaceutical composition of claim 1 , wherein the solid item is a troche.

10. The pharmaceutical composition of claim 1 , wherein the binder comprises a polyglycol or derivatives thereof having a molecular weight that is sufficient to provide suitable hardness and time for dissolution of the troche.

11. The pharmaceutical composition of claim 10 , wherein the polyglycol is selected from the group consisting of polyethylene glycol, polyethylene oxide, methoxypolyethylene glycol, polypropylene glycol and polybutylene glycol.

12. The pharmaceutical composition of claim 11 , wherein the excipient is selected from the group consisting of gelatin, sodium saccharin, stevioside, peppermint oil, cherry flavor, lemon oil, raspberry flavor and combinations thereof.

13. The pharmaceutical composition of claim 1 , wherein the binder comprises a product having a molecular weight that is sufficient to provide the necessary hardness and time for dissolution of the solid item, the binder being selected from the group consisting of methoxypolyethylene glycol, polypropylene glycol, polybutylene glycol, PEG-laureates, PEG-dilaureates, PEG-oleates, PEG-dioleates, PEG-trioleates, PEG-stearates, PEG-distearates, castor oil derivatives of PEG, palm kernel oil derivatives of PEG, corn oil derivatives of PEG, soya oil derivatives of PEG, cholesterol derivatives of PEG, phytosterol derivatives of PEG, caprate/caprylate glycerides derivatives of PEG, tocopheryl succinate derivatives of PEG, octylpheno derivatives of PEG, nonylphenol derivatives of PEG, polyglyceryl-10-laurate, polyglyceryl-10-oleate, POE-lauryl ethers, POE-oleyl ethers, POE-stearyl ethers, polysorbates, onostearate, monolaurate and monopalmitate derivatives of sucrose, and products of poly(oxypropylene)-co-poly(propylene oxide) family.

14. The pharmaceutical composition of claim 13 , further comprising a therapeutically effective quantity of a third pharmaceutically active compound selected from the group consisting of β-blockers, antiemetic medicaments, and combinations thereof, or pharmaceutically acceptable salts, hydrates, solvates or N-oxides thereof.

15. The pharmaceutical composition of claim 14 , wherein the β-blocker is selected from the group consisting of metoprolol, propranolol, acebutolol, nadolol, atenolol, betaxolol, esmolol, bisoprolol fumarate, carvedilol, nebivolol, penbutolol, timolol and sotalol.

16. The pharmaceutical composition of claim 14 , wherein the antiemetic medicament is selected from the group consisting of ondansentron, dolasetron, granisetron, palonosetron, promethazine, imenhydrinate, and meclizine.

17. The pharmaceutical composition of claim 14 , further comprising a therapeutically effective quantity of a receptor antagonist to benzodiazepines.

18. The pharmaceutical composition of claim 17 , wherein the receptor antagonist is flumazenil.

19. The pharmaceutical composition of claim 14 , wherein the first pharmaceutically active compound is medazolam, the second pharmaceutically active compound is ketamine and the third pharmaceutically active compound is metoprolol, wherein the medazolam:ketamine:metoprolol ratio is between about 1:2:1 and about 1:10:1 by mass.

20. The pharmaceutical composition of claim 14 , wherein the first pharmaceutically active compound is medazolam, the second pharmaceutically active compound is ketamine and the third pharmaceutically active compound is ondansentron, wherein the medazolam:ketamine: ondansentron ratio is about 3:25:2 by mass.

21. The pharmaceutical composition of claim 13 , wherein the excipient is selected from the group consisting of gelatin, sodium saccharin, stevioside, peppermint oil, cherry flavor, lemon oil, raspberry flavor and combinations thereof.

Assignments (10)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2025
From: MELT PHARMACEUTICALS, INC.
To: HARROW IP, LLC
Reel/Frame 073334/0195 →
RELEASE OF SECURITY INTEREST Recorded Feb 1, 2024
From: HARROW INC. F/K/A HARROW HEALTH, INC.
To: MELT PHARMACEUTICALS, INC.
Reel/Frame 066329/0616 →
SECURITY INTEREST Recorded Sep 2, 2021
From: MELT PHARMACEUTICALS, INC.
To: HARROW HEALTH, INC.
Reel/Frame 057368/0178 →
RELEASE OF SECURITY INTEREST Recorded May 7, 2021
From: SWK FUNDING LLC
To: HARROW IP, LLC
Reel/Frame 056174/0332 →
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Oct 9, 2020
From: SWK FUNDING LLC, AS COLLATERAL AGENT
To: HARROW IP, LLC
Reel/Frame 054037/0425 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Nov 21, 2019
From: HARROW IP, LLC
To: SWK FUNDING LLC, AS COLLATERAL AGENT
Reel/Frame 051079/0453 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2019
From: HARROW HEALTH, INC.
To: MELT PHARMACEUTICALS, INC.
Reel/Frame 049402/0961 →
CHANGE OF NAME Recorded Jan 4, 2019
From: IMPRIMIS PHARMACEUTICALS, INC.
To: HARROW HEALTH, INC.
Reel/Frame 048013/0368 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 19, 2017
From: IMPRIMIS PHARMACEUTICALS, INC.
To: SWK FUNDING LLC, AS COLLATERAL AGENT
Reel/Frame 043258/0581 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2016
From: BERDAHL, JOHN; WILEY, WILLIAM F.; SAADEH, DENNIS ELIAS
To: IMPRIMIS PHARMACEUTICALS, INC.
Reel/Frame 039925/0817 →
Continuity (2)
Provisional Application 62182130 · Jun 19, 2015
Related Publication 20160367566A1 · Dec 22, 2016