IP Library Granted Patent US 11,147,782
Granted Patent B1
US 11,147,782 · App. 17/210,064 · Granted Oct 19, 2021

GHB formulation and method for its manufacture

Inventors: Clark Allphin (Seattle, WA); Scott Bura (Gilroy, CA)
Assignee: JAZZ PHARMACEUTICALS IRELAND LIMITED
A61K31/19A61K9/5031A61K31/785A61K38/02
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Quick Facts
Patent No.
US 11,147,782
App. No.
17/210,064
Granted
Oct 19, 2021
Kind
B1
Abstract

The present application relates to GHB formulations and methods for manufacturing the same.

Claims (35)

1. A formulation of gamma-hydroxybutyrate comprising:

a plurality of immediate release particles comprising gamma-hydroxybutyrate;

a plurality of modified release particles comprising gamma-hydroxybutyrate;

a viscosity enhancing agent; and

an acid;

wherein the viscosity enhancing agent and the acid are separate from the immediate release particles and the modified release particles.

2. The formulation of claim 1 , wherein the viscosity enhancing agent is selected from the group consisting of xanthan gum, microcrystalline cellulose, hydroxyethyl cellulose, hydroxypropylmethyl cellulose, carboxymethylcellulose sodium, hydroxypropyl cellulose and mixtures thereof.

3. The formulation of claim 1 , wherein the acid is selected from the group consisting of malic acid, citric acid, tartaric acid, boric acid, maleic acid, phosphoric acid, and benzoic acid.

4. The formulation of claim 1 , wherein the formulation further comprises a lubricant selected from the group consisting of magnesium stearate, stearic acid, calcium stearate, hydrogenated castor oil, hydrogenated vegetable oil, light mineral oil, mineral oil, polyethylene glycol, sodium benzoate, sodium stearyl fumarate, and zinc stearate.

5. The formulation of claim 4 , wherein the lubricant is magnesium stearate.

6. The formulation of claim 1 , wherein the formulation comprises an amount of gamma-hydroxybutyrate equivalent to from 4.0 g to 12.0 g of sodium gamma-hydroxybutyrate.

7. The formulation of claim 1 , wherein the formulation comprises an amount of gamma-hydroxybutyrate equivalent to about 4.0 g, about 6 g, about 7.5 g or about 9 g of sodium gamma-hydroxybutyrate.

8. The formulation of claim 1 , wherein the formulation comprises an amount of gamma-hydroxybutyrate equivalent to about 6 g of sodium gamma-hydroxybutyrate.

9. The formulation of claim 1 , wherein the formulation comprises an amount of gamma-hydroxybutyrate equivalent to about 7.5 g of sodium gamma-hydroxybutyrate.

10. The formulation of claim 1 , wherein the formulation comprises an amount of gamma-hydroxybutyrate equivalent to about 9 g of sodium gamma-hydroxybutyrate.

11. The formulation of claim 1 , wherein 8 h after administration of the formulation provides a blood concentration ranging from 10 mg/L to about 40 mg/mL.

12. The formulation of claim 1 , wherein 8 h after administration of the formulation provides a blood concentration ranging from 15 mg/L to about 30 mg/mL.

13. The formulation of claim 1 , wherein the formulation is a multiparticulate composition.

14. A unit dose comprising a formulation of gamma-hydroxybutyrate,

wherein the formulation comprises:

a plurality of immediate release particles comprising gamma-hydroxybutyrate;

a plurality of modified release particles comprising gamma-hydroxybutyrate;

a viscosity enhancing agent; and

an acid;

wherein the viscosity enhancing agent and the acid are separate from the immediate release particles and the modified release particles.

15. The unit dose of claim 14 , wherein the viscosity enhancing agent is selected from the group consisting of xanthan gum, microcrystalline cellulose, hydroxyethyl cellulose, hydroxypropylmethyl cellulose, carboxymethylcellulose sodium, hydroxypropyl cellulose and mixtures thereof.

16. The unit dose of claim 14 , wherein the acid is selected from the group consisting of malic acid, citric acid, tartaric acid, boric acid, maleic acid, phosphoric acid, and benzoic acid.

17. The unit dose of claim 14 , wherein the formulation further comprises a lubricant selected from the group consisting of magnesium stearate, stearic acid, calcium stearate, hydrogenated castor oil, hydrogenated vegetable oil, light mineral oil, mineral oil, polyethylene glycol, sodium benzoate, sodium stearyl fumarate, and zinc stearate.

18. The unit dose of claim 17 , wherein the lubricant is magnesium stearate.

19. The unit dose of claim 14 , wherein 8 h after administration of the formulation provides a blood concentration ranging from 15 mg/L to about 30 mg/mL.

20. The unit dose of claim 14 , wherein the unit dose comprises an amount of gamma-hydroxybutyrate equivalent to from 4.0 g to 12.0 g of sodium gamma-hydroxybutyrate.

21. The unit dose of claim 14 , wherein unit dose contains an amount of gamma-hydroxybutyrate equivalent to about 6 g of sodium gamma-hydroxybutyrate.

22. The unit dose of claim 14 , wherein unit dose contains an amount of gamma-hydroxybutyrate equivalent to about 7.5 g of sodium gamma-hydroxybutyrate.

23. The unit dose of claim 14 , wherein unit dose contains an amount of gamma-hydroxybutyrate equivalent to about 9 g of sodium gamma-hydroxybutyrate.

24. The unit dose of claim 14 , wherein the unit dose is a sachet.

Assignments (3)
SECURITY AGREEMENT Recorded May 5, 2021
From: CAVION, INC.; CELATOR PHARMACEUTICALS, INC.; JAZZ PHARMACEUTICALS IRELAND LIMITED; JAZZ PHARMACEUTICALS, INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 056151/0010 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2021
From: JAZZ PHARMACEUTICALS, INC.
To: JAZZ PHARMACEUTICALS IRELAND LIMITED
Reel/Frame 055878/0435 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2021
From: ALLPHIN, CLARK; BURA, SCOTT
To: JAZZ PHARMACEUTICALS, INC.
Reel/Frame 055869/0727 →
Continuity (4)
Continuation 17118041 · Dec 10, 2020
Continuation 16448598 · Jun 21, 2019
Continuation 15047586 · Feb 18, 2016
Provisional Application 62117889 · Feb 18, 2015
Cited By (18)
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