Claims for Patent: 10,525,052

Summary for Patent: 10,525,052

Title:	Abuse-deterrent drug formulations
Abstract:	An abuse-deterrent pharmaceutical composition has been developed to reduce the likelihood of improper administration of drugs, especially drugs such as opiods. In the preferred embodiment, the drug is modified to increase its lipophilicity by forming a salt between the drug and one or more fatty acids wherein the concentration of the one or more fatty acids is one to 15 times the molar amount of the active agent, preferably two to ten times the molar amount of the active agent. In one embodiment the modified drug is homogeneously dispersed within microparticles composed of a material that is either slowly soluble or not soluble in water. In some embodiments the drug containing microparticles or drug particles are coated with one or more coating layers, where at least one coating is water insoluble and preferably organic solvent insoluble. The abuse-deterrent composition prevents the immediate release of a substantial portion of drug, even if the physical integrity of the formulation is compromised (for example, by chopping with a blade or crushing) and the resulting material is placed in water, snorted, or swallowed. However, when administered as directed, the drug is slowly released from the composition as the composition is broken down or dissolved gradually within the GI tract by a combination of enzymatic degradation, surfactant action of bile acids, and mechanical erosion.
Inventor(s):	Hirsh; Jane (Wellesley, MA), Fleming; Alison (Mansfield, MA), Rariy; Roman (Philadelphia, PA), Klibanov; Alexander (Boston, MA)
Assignee:	Collegium Pharmaceutical, Inc. (Stoughton, MA)
Application Number:	15/681,589
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 10,525,052
Patent Claims:	1. A pharmaceutical composition comprising solid microparticles, wherein the microparticles comprise: a. a therapeutically effective amount of oxycodone, b. one or more fatty acids, c. carnauba wax, and d. beeswax, wherein the carnauba wax and beeswax are present at about 25-40% by weight of the microparticles and the oxycodone is present as a fatty acid salt. 2. The composition of claim 1, wherein the one or more fatty acids is one or more C.sub.5 to C.sub.30 monovalent fatty acids selected from the group consisting of pentanoic acid, hexanoic (caproic) acid, heptanoic acid, octanoic (caprylic) acid, nonanoic acid, decanoic (capric) acid, undecanoic acid, dodecanoic (lauric) acid, tridecanoic acid, tetradecanoic (myristic) acid, pentadecanoic acid, hexadecanoic (palmitic) acid, heptadecanoic (margaric) acid, octadecanoic (stearic) acid, nonadecanoic acid, eicosanoic (arachidic) acid, heneicosanoic acid, docosanoic (behenic) acid, tricosanoic acid, tetracosanoic (lignoceric) acid, pentacosanoic acid, hexacosanoic acid, heptacosanoic acid, octacosanoic acid, nonacosanoic acid, triacontanoic acid, linoleic acid, oleic acid, and mixtures thereof. 3. The composition of claim 2, wherein the one or more fatty acids is selected from the group consisting of lauric, myristic, palmitic, stearic and mixtures thereof. 4. The composition of claim 3, wherein the one or more fatty acids is myristic acid. 5. The composition of claim 1, wherein the one or more fatty acids is myristic acid. 6. A pharmaceutical dosage form comprising the composition of claim 1. 7. A pharmaceutical dosage form comprising the composition of claim 4. 8. The pharmaceutical dosage form of claim 6, in the form of a capsule. 9. The pharmaceutical dosage form of claim 7, in the form of a capsule. 10. A method for the management of pain comprising administering to a patient in need thereof the pharmaceutical composition of claim 1. 11. A pharmaceutical composition comprising solid microparticles, wherein the microparticles comprise: a. a therapeutically effective amount of oxycodone, b. one or more fatty acids, c. carnauba wax, and d. beeswax, wherein the carnauba wax and beeswax are present at about 25-40% by weight of the microparticles and the oxycodone is present as a fatty acid salt; wherein the microparticles are prepared by a process comprising combining oxycodone base and one or more fatty acids at about 2 to 15 times the molar amount of oxycodone base; and wherein the one or more fatty acids and oxycodone base form the oxycodone fatty acid salt. 12. The composition of claim 11, wherein the process comprises combining oxycodone base and one or more fatty acids at about 2 to 10 times the molar amount of oxycodone base. 13. The composition of claim 11, wherein the process comprises combining oxycodone base and one or more fatty acids at about 6.9 to 15 times the molar amount of oxycodone base. 14. The composition of claim 11, wherein the process comprises combining oxycodone base and one or more fatty acids at about 6.9 to 10 times the molar amount of oxycodone base.