IP Library Granted Patent US 12,433,859
Granted Patent B2
US 12,433,859 · App. 18/792,999 · Granted Oct 7, 2025

Oral solutions comprising lisdexamfetamine salts

Inventors: Georgios Liolios (Chalandri Attica, GR); Ioannis Psarrakis (Lavrion, GR)
Assignee: Adalvo Limited
A61K31/165A61K9/0053A61K9/08
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Quick Facts
Patent No.
US 12,433,859
App. No.
18/792,999
Granted
Oct 7, 2025
Kind
B2
Abstract

Oral pharmaceutical solution comprising a pharmaceutically acceptable salt of lisdexamfetamine, and a pharmaceutically acceptable aqueous carrier comprising a buffer and a cosolvent selected from the group consisting of a glycol, a polyol, and a mixture thereof, wherein the pH of the solution is from 5.5 to 9.0. The oral pharmaceutical solution presents excellent physicochemical stability, even under alkaline conditions.

Claims (22)

1. An oral pharmaceutical solution comprising 10 mg/ml of lisdexamfetamine dimesylate and a pharmaceutically acceptable aqueous carrier comprising a buffer and a non-aqueous cosolvent selected from a glycol, a polyol and a mixture thereof, wherein the pH of the solution is from 6.0 to 9.0, and wherein the solution contains less than 1.0% total impurities after four weeks.

2. The oral pharmaceutical solution according to claim 1 , wherein the solution is free of any antioxidant.

3. The oral pharmaceutical solution according to claim 1 , wherein the solution is free of an antioxidant selected from the group consisting of sodium metabisulfite, butylated hydroxy anisole, butylated hydroxytoluene, ethylenediamine tetraacetic acid, ascorbic acid, α-tocopherol, and propyl gallate.

4. The oral pharmaceutical solution according to claim 1 , wherein the total concentration of the non-aqueous cosolvent is from 5 mg/ml to 300 mg/ml.

5. The oral pharmaceutical solution according to claim 1 , wherein the total concentration of the non-aqueous cosolvent is from 50 mg/ml to 250 mg/ml.

6. The oral pharmaceutical solution according to claim 1 , wherein the total concentration of the non-aqueous cosolvent is from 100 mg/ml to 200 mg/ml.

7. The oral pharmaceutical solution according to claim 1 , wherein the pH of the solution is from 6.0 to 8.5.

8. The oral pharmaceutical solution according to claim 1 , wherein the pH of the solution is from 6.5 to 8.0.

9. The oral pharmaceutical solution of claim 1 , wherein the oral solution comprises a second non-aqueous cosolvent.

10. The oral pharmaceutical solution of claim 1 , wherein the oral solution comprises an antimicrobial preservative.

11. The oral pharmaceutical solution of claim 1 , wherein the non-aqueous cosolvent is selected from maltitol, glycerol, mannitol, sorbitol, xylitol, propylene glycol, low molecular weight polyethylene glycol, and a mixture thereof.

12. The oral pharmaceutical solution of claim 1 , wherein the buffer is selected from ascorbic acid, acetic acid, tartaric acid, citric acid monohydrate, sodium citrate, potassium citrate, acetic acid, sodium acetate, sodium hydrogen phosphate, sodium dihydrogen phosphate, calcium hydrogen phosphate, calcium dihydrogen phosphate, and a mixture thereof.

13. The oral pharmaceutical solution according to claim 7 , wherein the total concentration of the non-aqueous cosolvent is from 5 mg/ml to 300 mg/ml.

14. The oral pharmaceutical solution according to claim 7 , wherein the total concentration of the non-aqueous cosolvent is from 50 mg/ml to 250 mg/ml.

15. The oral pharmaceutical solution according to claim 7 , wherein the total concentration of the non-aqueous cosolvent is from 100 mg/ml to 200 mg/ml.

16. The oral pharmaceutical solution of claim 7 , wherein the oral solution comprises an antimicrobial preservative.

17. The oral pharmaceutical solution of claim 7 , wherein the non-aqueous cosolvent is selected from maltitol, glycerol, mannitol, sorbitol, xylitol, propylene glycol, low molecular weight polyethylene glycol and a mixture thereof.

18. The oral pharmaceutical solution of claim 7 , wherein the buffer is selected from ascorbic acid, acetic acid, tartaric acid, citric acid monohydrate, sodium citrate, potassium citrate, acetic acid, sodium acetate, sodium hydrogen phosphate, sodium dihydrogen phosphate, calcium hydrogen phosphate, calcium dihydrogen phosphate, and a mixture thereof.

19. A method of treating Attention Deficit Hyperactivity Disorder in a subject in need thereof, the method comprising administering to the subject the oral pharmaceutical solution of claim 1 .

20. The method of claim 19 , wherein the subject is a child.

21. The oral pharmaceutical solution of claim 1 , wherein the solution contains less than 1.0% total impurities after four weeks at 40° C. and 75% relative humidity.

22. The method of claim 19 , wherein the solution contains less than 1.0% total impurities after four weeks of storage at 40° C. and 75% relative humidity.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2025
From: LABOMED PHARMACEUTICAL COMPANYS.A.
To: ADALVO LIMITED
Reel/Frame 069807/0404 →
CHANGE OF NAME Recorded Jan 9, 2025
From: LABOSERVE PHARMACEUTICAL COMPANY S.A.
To: LABOMED PHARMACEUTICAL COMPANY S.A.
Reel/Frame 069867/0850 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2025
From: LIOLIOS, GEORGIOS; PSARRAKIS, IOANNIS
To: LABOSERVE PHARMACEUTICAL COMPANY S.A.
Reel/Frame 069868/0085 →
Priority Claims (1)
EP 19386059 · Dec 30, 2019 · regional
Continuity (3)
Continuation 18167634 · Feb 10, 2023
Continuation 16961784
Related Publication 20240390304A1 · Nov 28, 2024
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