IP Library Granted Patent US 9,198,864
Granted Patent B2
US 9,198,864 · App. 14/735,526 · Granted Dec 1, 2015

Modified release formulations containing drug-ion exchange resin complexes

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Quick Facts
Patent No.
US 9,198,864
App. No.
14/735,526
Granted
Dec 1, 2015
Kind
B2
Abstract

A tablet comprising a coated drug-ion exchange resin complex composed of methylphenidate complexed with a pharmaceutically acceptable ion-exchange resin and an uncoated methylphenidate-ion exchange resin complex is provided. The coated methylphenidate-ion exchange resin complex is in admixture with a polymer to form a matrix. Also provided is a tablet comprising a coated drug-ion exchange resin complex composed of dexmethylphenidate complexed with a pharmaceutically acceptable ion-exchange resin and an uncoated dexmethylphenidate-ion exchange resin complex is provided. The coated dexmethylphenidate-ion exchange resin complex is in admixture with a polymer to form a matrix.

Claims (20)

1. A solid pharmaceutical orally disintegrating tablet comprising:

(a) drug-ion exchange resin complex particles that are uncoated and which comprise methylphenidate bound to an ion exchange resin, and

(b) modified release coated drug-ion exchange resin complex particles which comprise methylphenidate bound to an ion exchange resin, wherein said modified release coated drug-ion exchange resin complex particles (b) further comprise a hydrophilic polymer or water insoluble polymer or copolymer in a matrix with the drug-ion exchange resin complex, wherein the modified release coating is over the drug-ion exchange resin complex-matrix

wherein the weight ratio of (a) to (b) is about 2:1 to about 1:10.

2. The tablet according to claim 1 , wherein the modified release coating on the coated drug-ion exchange resin complex particles is a delayed release coating.

3. The tablet according to claim 1 , wherein said modified release coated drug-ion exchange resin complex particles (b) further comprise a water insoluble polymer or copolymer in a matrix with the drug-ion exchange resin complex, wherein the modified release coating is over the drug-ion exchange resin complex-matrix.

4. The tablet according to claim 3 , wherein the water insoluble polymer or copolymer is selected from the group consisting of a polyvinyl acetate polymer, cellulose acetate, acrylic based polymers or copolymers, cellulose phthalate, and mixtures thereof.

5. The tablet according to claim 1 , wherein the ion exchange resin in (a) and/or (b) is a strong acidic cation exchange resin.

6. The tablet according to claim 5 , wherein said strong acidic cation exchange resin is a sulfonated copolymer of a polystyrene crosslinked with divinylbenzyl.

7. The tablet according to claim 1 , wherein the drug-ion exchange resin complex particles of (a) and/or (b) have a particle size in the range of about 40 to about 250 microns.

8. A solid pharmaceutical orally disintegrating tablet comprising:

(a) drug-ion exchange resin complex particles that are uncoated and which comprise dexmethylphenidate bound to an ion exchange resin, and

(b) modified release coated drug-ion exchange resin complex particles which comprise dexmethylphenidate bound to an ion exchange resin, wherein said modified release coated drug-ion exchange resin complex particles (b) further comprise a hydrophilic polymer or water insoluble polymer or copolymer in a matrix with the drug-ion exchange resin complex, wherein the modified release coating is over the drug-ion exchange resin complex-matrix

wherein the weight ratio of (a) to (b) is about 2:1 to about 1:10.

9. The tablet according to claim 8 , wherein the modified release coating on the coated drug-ion exchange resin complex particles is a delayed release coating.

10. The tablet according to claim 8 , wherein said modified release coated drug-ion exchange resin complex particles (b) further comprise a water insoluble polymer or copolymer in a matrix with the drug-ion exchange resin complex, wherein the modified release coating is over the drug-ion exchange resin complex-matrix.

11. The tablet according to claim 10 , wherein the water insoluble polymer or copolymer is selected from the group consisting of a polyvinyl acetate polymer, cellulose acetate, acrylic based polymers or copolymers, cellulose phthalate, and mixtures thereof.

12. The tablet according to claim 8 , wherein the ion exchange resin in (a) and/or (b) is a strong acidic cation exchange resin.

13. The tablet according to claim 12 , wherein said strong acidic cation exchange resin is a sulfonated copolymer of a polystyrene crosslinked with divinylbenzyl.

14. The tablet according to claim 8 , wherein the drug-ion exchange resin complex particles of (a) and/or (b) have a particle size in the range of about 40 to about 250 microns.

Assignments (5)
SECURITY INTEREST Recorded Sep 26, 2024
From: TRIS PHARMA, INC.; PARK THERAPEUTICS, INC.
To: PROVIDENT BANK
Reel/Frame 069065/0576 →
NOTICE OF RELEASE OF SECURITY INTEREST IN PATENTS Recorded Sep 25, 2018
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: TRIS PHARMA, INC.
Reel/Frame 047150/0169 →
GRANT OF SECURITY INTEREST IN PATENT RIGHTS Recorded Sep 24, 2018
From: TRIS PHARMA, INC.
To: DEERFIELD MANAGEMENT COMPANY, L.P., AS THE AGENT
Reel/Frame 047140/0290 →
PATENT SECURITY AGREEMENT Recorded Sep 5, 2017
From: TRIS PHARMA, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 043761/0389 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 14, 2015
From: MEHTA, KETAN; TU, YU-HSING
To: TRIS PHARMA, INC.
Reel/Frame 036791/0031 →