Granted Patent B2

US 12,396,955 · App. 19/174,583 · Granted Aug 26, 2025

Inventors: William H. McKenna (Yonkers, NY); Richard O. Mannion (Furlong, PA); Edward P. O'Donnell (Basking Ridge, NJ); Haiyong H. Huang (Princeton, NJ)

Assignees: PURDUE PHARMA L.P.; PURDUE PHARMACEUTICALS L.P.

A61K9/28A61J3/005A61J3/06A61J3/10A61K9/0002A61K9/0053A61K9/1641A61K9/2013A61K9/2018A61K9/2027A61K9/2031A61K9/2054A61K9/2077A61K9/209A61K9/2095A61K9/284A61K9/2853A61K9/2866A61K9/2893A61K31/485A61K45/06A61K47/10A61K47/34B29B7/02B29B7/88B29C35/045B29C35/16B29C37/0025B29C43/003B29C43/02B29C43/52B29C71/00B29C71/009A61K9/2072B29C2035/046B29C2035/1658B29K2071/02B29K2105/0035B29K2105/251B29K2995/0088B29L2031/753

Abstract

Claims (42)

1. A process of preparing a solid oral extended release pharmaceutical dosage form, comprising:

(a) combining (1) at least one polyethylene oxide (PEO) having an approximate molecular weight of about 1 million Da to about 15 million Da based on rheological measurements, and (2) oxycodone or a pharmaceutically acceptable salt thereof, to form a mixture;

(b) blending the mixture to form a blend;

(c) compressing the blend in a press to form uncured dosage forms; and

(d) curing the dosage forms in step (c) to form cured dosage forms, wherein the curing temperature is at least about 80° C.; wherein the uncured and cured dosage forms are both in a form of tablets;

wherein the PEO comprises at least about 30% (by weight) of the total weight of the solid oral extended release pharmaceutical dosage form;

wherein the solid oral extended release pharmaceutical dosage form comprises about 10 mg, about 15 mg, about 20 mg, about 30 mg, about 40 mg, about 60 mg or about 80 mg of the oxycodone or pharmaceutically acceptable salt thereof;

wherein the solid oral extended release pharmaceutical dosage form provides a mean tmax of oxycodone at about 2 to about 6 hours after administration to a human subject; and

wherein the solid oral extended release pharmaceutical dosage form is resistant to alcohol extraction.

2. The process of claim 1 , wherein the solid oral extended release pharmaceutical dosage form comprises oxycodone hydrochloride.

3. The process of claim 1 , wherein the administration of the solid oral extended release pharmaceutical dosage form provides a mean maximum plasma concentration (C max ) of oxycodone from about 6 ng/ml to about 240 ng/mL.

4. The process of claim 1 , wherein the polyethylene oxide (PEO) has an approximate molecular weight of about 2 million Da to about 8 million Da based on rheological measurements.

5. The process of claim 1 , wherein the polyethylene oxide (PEO) has an approximate molecular weight of about 5 million Da based on rheological measurements.

6. The process of claim 1 , wherein the polyethylene oxide (PEO) has an approximate molecular weight of about 7 million Da based on rheological measurements.

7. The process of claim 1 , wherein the mixture further comprises an anti-tacking agent.

8. The process of claim 7 , wherein the anti-tacking agent comprises magnesium stearate.

9. The process of claim 1 , wherein the density of the cured dosage form in comparison to the density of the uncured dosage form decreases by at least about 0.5%.

10. The process of claim 1 , wherein the density of the cured dosage form in comparison to the density of the uncured dosage form decreases by at least about 0.7%.

11. The process of claim 1 , wherein the density of the cured dosage form in comparison to the density of the uncured dosage form decreases by at least about 0.8%.

12. The process of claim 1 , wherein the density of the cured dosage form in comparison to the density of the uncured dosage form decreases by at least about 1.0%.

13. The process of claim 1 , wherein the density of the cured dosage form in comparison to the density of the uncured dosage form decreases by at least about 2.0%.

14. The process of claim 1 , wherein the density of the cured dosage form in comparison to the density of the uncured dosage form decreases by at least about 2.5%.

15. The process of claim 1 , wherein the solid oral extended release pharmaceutical dosage form provides an in-vitro dissolution rate, which when measured in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C., is between 12.5 and 55% (by wt) of the oxycodone or pharmaceutically acceptable salt thereof released after 1 hour, between 25 and 65% (by wt) of the oxycodone or pharmaceutically acceptable salt thereof released after 2 hours, between 45 and 85% (by wt) of the oxycodone or pharmaceutically acceptable salt thereof released after 4 hours and between 55 and 95% (by wt) of the oxycodone or pharmaceutically acceptable salt thereof released after 6 hours.

16. The process of claim 1 , wherein the solid oral extended release pharmaceutical dosage form provides an in-vitro dissolution rate, when measured in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) comprising 40% ethanol at 37° C., characterized by the percent amount of the oxycodone or pharmaceutically acceptable salt thereof released at 0.5 hours, that deviates no more than about 20% points 0.5 hours from the corresponding in-vitro dissolution rate measured in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C. without ethanol.

17. The process of claim 1 , wherein the curing is for a time period from about 15 minutes to about 10 hours.

18. The solid oral extended release dosage form of claim 1 , wherein the curing is for a time period from about 30 minutes to about 20 hours.

19. The process of claim 1 , wherein the cured dosage forms, when subjected to a maximum force of about 196 N in a tablet hardness test, does not break.

20. The process of claim 1 , wherein the cured dosage forms, when subjected to an indentation test resists a work of at least about 0.06 J, does not crack.

21. The process of claim 1 , wherein the solid oral extended release pharmaceutical dosage form does not comprise polyethylene oxide having an approximate molecular weight of less than 1 million Da based on rheological measurements.

22. The process of claim 1 , further comprising cooling the cured dosage forms after curing the uncured tablets.

23. The process of claim 1 , comprising cooling the cured dosage forms to a temperature below about 50° C.

24. A process of preparing a solid oral extended release pharmaceutical dosage form, comprising:

(a) combining

(1) at least one polyethylene oxide (PEO) having an approximate molecular weight of about 2 million Da to about 8 million Da based on rheological measurements, and

(2) oxycodone or a pharmaceutically acceptable salt thereof, to form a mixture;

(b) blending the mixture to form a blend;

(c) compressing the blend in a press to form uncured dosage forms; and

(d) curing the dosage forms in step (c) to form cured dosage forms, wherein the curing temperature is at least about 80° C.;

wherein the uncured and cured dosage forms are both in a form of tablets;

wherein the PEO comprises at least about 30% (by weight) of the total weight of the solid oral extended release pharmaceutical dosage form;

wherein the solid oral extended release pharmaceutical dosage form comprises about 10 mg, about 15 mg, about 20 mg, about 30 mg, about 40 mg, about 60 mg or about 80 mg of the oxycodone or pharmaceutically acceptable salt thereof;

wherein the solid oral extended release pharmaceutical dosage form provides a mean t max of oxycodone at about 2 to about 6 hours after administration to a human subject; and wherein the solid oral extended release pharmaceutical dosage form provides an in-vitro dissolution rate, when measured in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) comprising 40% ethanol at 37° C., characterized by the percent amount of the oxycodone or pharmaceutically acceptable salt thereof released at 0.5 hours, that deviates no more than about 20% points 0.5 hours from the corresponding in-vitro dissolution rate measured in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C. without ethanol.

Assignments (1)

Continuity (18)

References Cited (400)