IP Library Granted Patent US 8,563,014
Granted Patent B2
US 8,563,014 · App. 13/094,578 · Granted Oct 22, 2013

Modafinil oral lyophilizate

Inventors: Thanh-Tam Nguyen (Limeil-Brevannes, FR); Joëlle Leyder (Creteil, FR)
Assignee: Teva Sante
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Quick Facts
Patent No.
US 8,563,014
App. No.
13/094,578
Granted
Oct 22, 2013
Kind
B2
Abstract

The invention concerns an oral lyophilizate comprising modafinil particles having a median diameter of about 10 to about 1000 μm in association with an appropriate amount of at least one excipient selected from the group consisting of fatty acid esters of glycerol, cyclic oligosaccharides, sweeteners or mixtures thereof.

Claims (18)

1. A method for the manufacture of an oral lyophilizate comprising taste masked modafinil particles, comprising the steps of:

(i) coating modafinil particles having a median diameter of less than 200 μm with a fatty acid ester of glycerol to provide taste masked modafinil particles;

(ii) preparing a water suspension comprising the taste masked modafinil particles; and

(iii) lyophilizing the suspension;

wherein when the oral lyophilizate is introduced into 1 L of 0.1M HCl at 37° C. more than 75% by weight of the modafinil dissolves in 30 minutes.

2. The method according to claim 1 , wherein the fatty acid ester of glycerol is chosen from fatty acid monoglycerides, fatty acid diglycerides, fatty acid triglycerides, and mixtures thereof.

3. The method according to claim 2 , wherein the fatty acid ester of glycerol is derived from dibehenic acid, palmitostearic acid, stearic acid, oleic acid, linoleic acid, caprylic acid, capric acid, or mixtures thereof.

4. The method according to claim 1 , wherein the modafinil is the levorotatory isomer of modafinil.

5. The method according to claim 1 , wherein the modafinil is the dextrorotatory isomer of modafinil.

6. The method according to claim 1 , wherein when the oral lyophilizate is introduced into 1 L of 0.1 M HCl at 37° C. more than 85% by weight of the modafinil dissolves in 30 minutes.

7. The method according to claim 1 , wherein the modafinil particles have a median diameter of between 20 and 40 μm.

8. The method according to claim 1 , wherein the oral lyophilizate comprises about 50 mg to about 850 mg of modafinil.

9. The method according to claim 1 , wherein when the oral lyophilizate is introduced into 1 L of 0.1 M HCl at 37° C. more than 80% by weight of the modafinil dissolves in 10 minutes.

10. The method according to claim 1 , wherein when the oral lyophilizate is introduced into 1 L of 0.1 M HCl at 37° C. more than 90% by weight of the modafinil dissolves in 15 minutes.

11. The method according to claim 1 , wherein the oral lyophilizate has a disintegration time of less than 3 minutes, as measured according to the USP method (<701> USP 26).

12. The method according to claim 1 , wherein the oral lyophilizate has a disintegration time of 2 to 60 seconds, as measured according to the USP method (<701> USP 26).

13. The method according to claim 1 , wherein the oral lyophilizate has a hardness of 5 N to 60 N as measured with the Schleuniger® apparatus (Schleuniger, Switzerland).

14. The method according to claim 1 , wherein the oral lyophilizate has a hardness of 7 N to 30 N as measured with the Schleuniger® apparatus (Schleuniger, Switzerland).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2013
From: NGUYEN, THANH-TAM; LEYDER, JOELLE
To: CEPHALON FRANCE
Reel/Frame 029973/0952 →
MERGER Recorded Jan 24, 2013
From: CEPHALON FRANCE
To: TEVA SANTE
Reel/Frame 029692/0457 →
Priority Claims (1)
EP 04291946 · Jul 29, 2004 · regional
Continuity (3)
Continuation 11191559 · Jul 28, 2005
Provisional Application 60598553 · Aug 4, 2004
Related Publication 20110229578A1 · Sep 22, 2011