IP Library Granted Patent US 10,874,624
Granted Patent B2
US 10,874,624 · App. 15/548,345 · Granted Dec 29, 2020

Stable trientine formulations

Inventor: Samuel D. Waksal (New York, NY)
Assignee: KADMON PHARMACEUTICALS, LLC
A61K31/132A61K31/13A61K45/06
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Quick Facts
Patent No.
US 10,874,624
App. No.
15/548,345
Granted
Dec 29, 2020
Kind
B2
Abstract

Provided are pharmaceutical dosage forms comprising (i) trientine or a pharmaceutically acceptable salt of trientine, in a (ii) sealed packaging. The sealed packaging provides a high barrier protection against air, moisture and light and prevents exposure of the drug to conditions that facilitate its decomposition. The pharmaceutical dosage forms are useful for treating diseases or conditions where excess copper is not removed from the body, e.g., Wilson's disease.

Claims (19)

1. A solid oral dosage form comprising (i) trientine or a pharmaceutically acceptable salt of trientine, in a (ii) sealed packaging wherein the sealed packaging contains a single-use quantity of the trientine as a capsule or tablet packaged in an inert atmosphere.

2. The solid oral dosage form of claim 1 where the inert atmosphere is nitrogen.

3. The solid oral dosage form of claim 1 where degradation of the trientine is substantially prevented at ambient (i.e. room) temperatures (20-25° C.).

4. The solid oral dosage form of claim 3 where trientine is in the free base form.

5. The solid oral dosage form of claim 3 where trientine is in the form of the hydrochloride, dihydrochloride, hydrobromide, sulfate, bisulfate, phosphate, nitrate, acetate, stearate, laurate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, napthylate, or mesylate salt of trientine.

6. The solid oral dosage form of claim 3 where trientine is in the form of the hydrochloride or dihydrochloride salt of trientine.

7. The solid oral dosage form of claim 3 further comprising an amine-based chelator that is not trientine or a pharmaceutically acceptable salt of trientine, an oxygen scavenger, or a desiccant.

8. The solid oral dosage form of claim 3 wherein the dosage form is provided in a blister pack.

9. The solid oral dosage form of claim 3 where the sealed packaging is formed from one or more materials comprising aluminum, aluminum foil laminates, polymers, polymer film laminates, or paper laminates.

10. The solid oral dosage form of claim 3 where the sealed packaging is formed from a polymer selected from the group consisting of PETs, polyethylene, and polypropylene.

11. The solid oral dosage form of claim 3 where the sealed packaging contains a single therapeutic dose of trientine.

12. The solid oral dosage form of claim 1 where the trientine is present in a tablet or capsule disposed within a blister pack.

13. The solid oral dosage form of claim 1 comprising 250 mg of trientine.

14. A method of making the solid oral dosage form of claim 1 comprising packaging trientine under an inert atmosphere that excludes oxygen and moisture.

15. The method of claim 14 where the inert atmosphere is nitrogen.

16. A method of treating a disease or condition where excess copper is not removed from the body by administering to a patient in need thereof the solid oral dosage form of claim 3 .

17. The method of claim 16 where the patient is a human.

18. The method of claim 17 where the disease or condition is Wilson's disease.

19. The method of claim 18 where the solid oral dosage form comprises 250 mg of trientine.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2018
From: WAKSAL, SAMUEL D.
To: KADMON PHARMACEUTICALS, LLC
Reel/Frame 045720/0684 →
Continuity (2)
Provisional Application 62111522 · Feb 3, 2015
Related Publication 20180015053A1 · Jan 18, 2018