IP Library Granted Patent US 10,653,629
Granted Patent B2
US 10,653,629 · App. 15/885,231 · Granted May 19, 2020

Single layer oral dose of neuro-attenuating ketamine

Inventors: Alex Nivorozhkin (West Roxbury, MA); Nelson Landrau (Marlborough, MA)
Assignee: Amorsa Therapeutics, Inc.
A61K9/2059A61K9/2013A61K9/2027A61K9/2031A61K9/2054A61K31/135A61K31/13
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Quick Facts
Patent No.
US 10,653,629
App. No.
15/885,231
Granted
May 19, 2020
Kind
B2
Abstract

The present invention is directed to oral neuro-attenuating ketamine (NAKET) tablet formulations, and methods of administration, which ensure the steady release of a therapeutically effective concentration of ketamine from an oral tablet without neurologically toxic spikes in ketamine concentration. In particular, the present invention provides single layer oral tablet formulation of NAKET. In a specific embodiment, the NAKET tablet formulation, and methods of administration provide steady administration of NAKET to a subject for 24 hours or greater, for example, up to 36 hours, after a single administration event.

Claims (26)

1. A single-layer orally administered tablet composition comprising neuro-attenuating ketamine (NAKET) and a polymer.

2. The tablet composition of claim 1 , wherein the composition is adapted for maximum sustained release.

3. The tablet composition of claim 1 , wherein the tablet composition comprises NAKET comprises a combination of (i) a water-insoluble neutrally charged non-ionic matrix; (ii) a polymer carrying one or more negatively charged groups; and (iii) ketamine.

4. The tablet composition of claim 3 , wherein the non-ionic matrix is selected from cellulose-based polymers, alone or enhanced by mixing with components selected from the group consisting of starches; waxes; neutral gums; polymethacrylates; PVA; PVA/PVP blends; and mixtures thereof.

5. The tablet composition of claim 4 , wherein the cellulose-based polymer is hydroxypropyl methylcellulose (HPMC).

6. The tablet composition of claim 1 , wherein the polymer carrying one or more negatively charged groups is selected from the group consisting of polyacrylic acid, polylactic acid, polyglycolic acid, polymethacrylate carboxylates, cation-exchange resins, clays, zeolites, hyaluronic acid, anionic gums, salts thereof, and mixtures thereof.

7. The tablet composition of claim 6 , wherein the anionic gum is selected from the group consisting of naturally occurring materials and semi-synthetic materials.

8. The tablet composition of claim 7 , wherein the naturally occurring material is selected from the group consisting of alginic acid, pectin, xanthan gum, carrageenan, locust bean gum, gum arabic, gum karaya, guar gum, and gum tragacanth.

9. The tablet composition of claim 7 , wherein the semi-synthetic material is selected from the group consisting of carboxymethyl-chitin and cellulose gum.

10. The tablet composition of claim 1 , comprising an amount of ketamine therapeutically effective for the treatment of pain.

11. The tablet composition of claim 1 , comprising an amount of ketamine therapeutically effective for use in the treatment of brain injury.

12. The tablet composition of claim 1 , comprising an amount of ketamine therapeutically effective for the treatment of depression.

13. The tablet composition of claim 1 , wherein the neuro-attenuating ketamine achieves a combined concentration of ketamine and its metabolite norketamine in plasma in the range of 10-500 ng/ml, and maintains this concentration for duration of the release period.

14. The tablet composition of claim 1 , wherein the polymer comprises one or more negatively charged groups.

15. A tablet composition formulated for oral administration comprising: ketamine and a polymer.

16. The tablet of claim 15 wherein the polymer comprises one or more negatively charged groups.

17. The tablet of claim 15 wherein the polymer comprises one or more acid groups.

18. The tablet of claim 17 wherein the polymer comprises a water-insoluble neutrally charged non-ionic matrix.

19. The table of claim 18 wherein the non-ionic matrix is selected from cellulose-based polymers, alone or enhanced by mixing with components selected from the group consisting of starches; waxes; neutral gums; polymethacrylates; PVA; PVA/PVP blends; and mixtures thereof.

20. The tablet composition of claim 19 , wherein the cellulose-based polymer is hydroxypropyl methylcellulose (HPMC).

21. A kit for the treatment of a subject with ketamine comprising 1) a single-layer orally administered tablet composition of claim 1 2) and instructions for use in the treatment of pain.

22. A kit for the treatment of a subject with ketamine comprising 1) a single-layer orally administered tablet composition of claim 1 and 2) instructions for use in the treatment of brain injury.

23. A kit for the treatment of a subject with ketamine comprising 1) a single-layer orally administered tablet composition of claim 1 and 2) instructions for use in the treatment of depression.

24. The kit of claim 21 , wherein the polymer comprises one or more negatively charged groups.

25. The kit of claim 22 , wherein the polymer comprises one or more negatively charged groups.

26. The kit of claim 23 , wherein the polymer comprises one or more negatively charged groups.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2024
From: AMORSA THERAPEUTICS, INC.
To: ACADIA PHARMACEUTICALS INC.
Reel/Frame 068048/0896 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2018
From: NIVOROZHKIN, ALEX, MR.; LANDRAU, NELSON, MR.
To: AMORSA THERAPEUTICS, INC.
Reel/Frame 044789/0428 →
Continuity (4)
Division 14914416
Provisional Application 62015513 · Jun 22, 2014
Provisional Application 61869884 · Aug 26, 2013
Related Publication 20180153813A1 · Jun 7, 2018
Cited By (3)
US 12,280,022 US 12,336,970 US 12,514,831