Claims for Patent: 9,968,598

Summary for Patent: 9,968,598

Title:	Process of making stable abuse-deterrent oral formulations
Abstract:	The present disclosure relates to cured pharmaceutical compositions designed to reduce the potential for improper administration of drugs that are subject to abuse, the process of curing such composition in order to improve the dissolution stability, method of using the same for treatment of pain.
Inventor(s):	Saim; Said (Wrentham, MA), Fleming; Alison B. (Mansfield, MA), Varanasi; Ravi K. (Walpole, MA)
Assignee:	Collegium Pharmaceutical, Inc. (Canton, MA)
Application Number:	15/649,024
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 9,968,598
Patent Claims:	1. A process comprising: a. preparing a mixture comprising: (i) oxycodone, myristic acid, beeswax and carnauba wax, or (ii) oxycodone in the form of a fatty acid salt, beeswax and carnauba wax at a temperature sufficient to form a substantially homogeneous melt; b. forming solid microparticles from the substantially homogeneous melt; c. optionally further formulating the solid microparticles with additional pharmaceutically acceptable excipients, and d. curing the solid microparticles or formulated microparticles at a temperature within the range of 25.degree. C. up to and including the inversion temperature, for a minimum of about 48 hours. 2. The process of claim 1, wherein the cured formulated microparticles exhibit less change in the dissolution profile after storage for 6 months at 25.degree. C. and 60% RH than otherwise identical uncured formulated microparticles after storage for 6 months at 25.degree. C. and 60% RH, wherein dissolution is conducted at 100 RPM using USP Apparatus I in 900 mL of pH 4.5 sodium acetate buffer supplemented with 0.03% Tween 20 at 37.degree. C. 3. The process of claim 1, wherein the cured microparticles or cured formulated microparticles exhibit less than a 15% change in the mean percent drug released at the 4 hour dissolution time point after storage for 6 months at 25.degree. C. and 60% RH, and wherein dissolution is conducted using USP Apparatus I in pH 4.5 sodium acetate buffer supplemented with 0.03% Tween 20. 4. The process of claim 1, wherein the cured microparticles or cured formulated microparticles exhibit less than a 10% change in the mean percent drug released at the 4 hour dissolution time point after storage for 6 months at 25.degree. C. and 60% RH, and wherein dissolution is conducted using USP Apparatus I in pH 4.5 sodium acetate buffer supplemented with 0.03% Tween 20. 5. The process of claim 1, wherein the cured microparticles or cured formulated microparticles exhibit less than a 5% change in the mean percent drug released at the 4 hour dissolution time point after storage for 6 months at 25.degree. C. and 60% RH, and wherein dissolution is conducted using USP Apparatus I in pH 4.5 sodium acetate buffer supplemented with 0.03% Tween 20. 6. The process of claim 1, wherein the cured microparticles or cured formulated microparticles exhibit less than a 2.5% change in the mean percent drug released at the 4 hour dissolution time point after storage for 6 months at 25.degree. C. and 60% RH, and wherein dissolution is conducted using USP Apparatus I in pH 4.5 sodium acetate buffer supplemented with 0.03% Tween 20. 7. The process of claim 1, wherein the inversion temperature is approximately 36.degree. C. 8. The process of claim 1, wherein the microparticles or formulated microparticles are cured at a first temperature above the inversion temperature and subsequently a second temperature below the inversion temperature. 9. A pharmaceutical composition prepared by the process of claim 1. 10. The pharmaceutical composition of claim 9, comprising about 9 mg to about 72 mg oxycodone or an equivalent amount of fatty acid salt thereof. 11. The pharmaceutical composition of claim 9, comprising about 9 mg to about 36 mg oxycodone or an equivalent amount of a fatty acid salt thereof. 12. The pharmaceutical composition of claim 9, comprising myristic acid in about 30 wt. % to about 70 wt. % of the pharmaceutical composition. 13. The pharmaceutical composition of claim 9, comprising myristic acid in about 40 wt. % to about 60 wt. % of the pharmaceutical composition. 14. The pharmaceutical composition of claim 9, wherein the combination of beeswax and carnauba wax comprises about 20 wt. % to about 60 wt. % of the pharmaceutical composition. 15. The pharmaceutical composition of claim 9, wherein the combination of beeswax and carnauba wax comprises about 30 wt. % to about 50 wt. % of the pharmaceutical composition. 16. The pharmaceutical composition of claim 9, comprising: a. about 9 mg to about 72 mg oxycodone or an equivalent amount of a fatty acid salt thereof; b. about 30 wt. % to about 70 wt. % of myristic acid; and c. about 20 wt. % to about 60 wt. % of a combination of beeswax and carnauba wax. 17. The pharmaceutical composition of claim 9, comprising: a. about 9 mg to about 72 mg oxycodone or an equivalent amount of a fatty acid salt thereof; b. about 40 wt. % to about 60 wt. % of myristic acid; and c. about 30 wt. % to about 50 wt. % of a combination of beeswax and carnauba wax. 18. The pharmaceutical composition of claim 9, comprising: a. about 9 mg to about 36 mg oxycodone or an equivalent amount of a fatty acid salt thereof; b. about 40 wt. % to about 60 wt. % of myristic acid; and c. about 30 wt. % to about 50 wt. % of a combination of beeswax and carnauba wax. 19. A capsule comprising the pharmaceutical composition of claim 9. 20. A capsule comprising the pharmaceutical composition of claim 16. 21. A capsule comprising the pharmaceutical composition of claim 17. 22. A capsule comprising the pharmaceutical composition of claim 18. 23. Pharmaceutically acceptable solid microparticles or formulated microparticles comprising: a mixture prepared from a homogeneous melt comprising beeswax, carnauba wax, oxycodone or a myristate salt of oxycodone, and a sufficient amount of myristic acid to provide said microparticles in substantially homogeneous form; wherein said microparticles or formulated microparticles are cured at one or more temperatures within the range of 25.degree. C. up to and including the inversion temperature, for a minimum of about 48 hour. 24. A method of treating pain comprising administering the pharmaceutical composition of claim 9 to a patient in need thereof. 25. A method of treating pain comprising administering the pharmaceutical composition of claim 16 to a patient in need thereof. 26. A method of treating pain comprising administering the pharmaceutical composition of claim 18 to a patient in need thereof. 27. A method of treating pain comprising administering the capsule of claim 19 to a patient in need thereof. 28. A method of treating pain comprising administering the capsule of claim 20 to a patient in need thereof. 29. A method of treating pain comprising administering the capsule of claim 22 to a patient in need thereof. 30. A method of treating pain comprising administering the pharmaceutically acceptable microparticles or formulated microparticles of claim 23 to a patient in need thereof.