IP Library Granted Patent US 8,557,995
Granted Patent B2
US 8,557,995 · App. 13/154,562 · Granted Oct 15, 2013

Solid dispersions containing kinase inhibitors

Inventors: Jonathan M. Miller (Lindenhurst, IL); Rajeev Gokhale (Helios, SG); Eric A. Schmitt (Libertyville, IL); Yi Gao (Vernon Hills, IL); Justin Lafountaine (Chicago, IL); Lloyd Dias (Gurnee, IL)
Assignee: AbbVie Inc.
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Quick Facts
Patent No.
US 8,557,995
App. No.
13/154,562
Granted
Oct 15, 2013
Kind
B2
Abstract

A solid dispersion comprises, in essentially non-crystalline form, a kinase inhibitory compound, e.g., N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises dissolving the compound, the polymeric carrier and the surfactant in a suitable solvent, and removing the solvent to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a cancer.

Claims (16)

1. A solid dispersion product comprising N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno [3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea or a pharmaceutically acceptable salt thereof, at least one pharmaceutically acceptable water-soluble polymeric carrier, and at least one pharmaceutically acceptable surfactant, wherein the N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea is present in about 1% to about 40% by free base equivalent weight.

2. The solid dispersion product of claim 1 , wherein solid dispersion product is amorphous.

3. The solid dispersion product of claim 1 , comprising at least one acid.

4. The solid dispersion product of claim 3 , wherein the at least one acid comprises from about 0.1 to about 10 equivalents with respect to N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno [3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea.

5. The solid dispersion product of claim 3 , wherein the at least one acid is selected from the group consisting of acetic acid, ascorbic acid, benzenesulfonic acid, citric acid, ethanedisulfonic acid, 1-hydroxy-2-napthoic acid, hydrochloric acid, hydrobromic acid, lactic acid, maleic acid, malic acid, malonic acid, methanesulfonic acid, phosphoric acid, sulfuric acid, succinic acid, tartaric acid, and toluenesulfonic acid.

6. The solid dispersion product of claim 3 , wherein the at least one acid is selected from the group consisting of citric acid, maleic acid, malic acid, malonic acid, succinic acid, and tartaric acid.

7. The solid dispersion product of claim 3 , wherein the at least one acid is citric acid.

8. The solid dispersion product of claim 1 , wherein the N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea is present in about 5% to about 15% by free base equivalent weight.

9. The solid dispersion product of claim 1 , wherein the N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea is present in about 8% to about 12% by free base equivalent weight.

10. The solid dispersion product of claim 1 , wherein the at least one polymeric carrier is present in an amount of about 40% to about 85% by weight and the at least one surfactant is present in an amount of about 5% to about 30% by weight.

11. The solid dispersion product of claim 1 , wherein at least one polymeric carrier is selected from the group consisting of homopolymers and copolymers of N-vinyl lactams, cellulose esters, cellulose ethers, high molecular weight polyalkylene oxides, polyacrylates, polymethacrylates, polyacrylamides, vinyl acetate polymers, oligo- and polysaccharides, and mixtures thereof.

12. The solid dispersion product of claim 1 , wherein the at least one polymeric carrier is selected from the group consisting of polyvinylpyrrolidone, hydroxypropyl methylcellulose, and mixtures thereof.

13. The solid dispersion product of claim 1 , wherein the at least one surfactant is selected from the group consisting of polyethylene glycol glyceride derivatives, polyoxyethylene castor oil derivatives, fatty acid monoesters of sorbitan, polysorbates, poloxamers, α-tocopheryl polyethylene, glycol succinate, and mixtures thereof.

14. The solid dispersion product of claim 1 , wherein the at least one surfactant is selected from the group consisting of polysorbates, polyoxyethylene castor oil derivatives, and mixtures thereof.

15. An orally deliverable pharmaceutical dosage form comprising the solid dispersion product of claim 1 .

16. The dosage form of claim 15 , containing at least one additive selected from the disintegrants, lubricants, and bulking agents.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030089/0600 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2011
From: MILLER, JONATHAN; GOKHALE, RAJEEV; SCHMITT, ERIC A.; GAO, YI; JUSTIN LAFOUNTAINE; DIAS, LLOYD
To: ABBOTT LABORATORIES
Reel/Frame 026418/0031 →
Continuity (2)
Provisional Application 61352862 · Jun 9, 2010
Related Publication 20110306632A1 · Dec 15, 2011