Claims for Patent: 9,132,125

Summary for Patent: 9,132,125

Title:	Benzoic acid, benzoic acid derivatives and heteroaryl carboxylic acid conjugates of hydrocodone, prodrugs, methods of making and use thereof
Abstract:	The presently described technology provides compositions comprising aryl carboxylic acids chemically conjugated to hydrocodone (morphinan-6-one, 4,5-alpha-epoxy-3-methoxy-17-methyl) to form novel prodrugs/compositions of hydrocodone, including benzoates and heteroaryl carboxylic acids, which have a decreased potential for abuse of hydrocodone. The present technology also provides methods of treating patients, pharmaceutical kits and methods of synthesizing conjugates of the present technology.
Inventor(s):	Mickle; Travis (Celebration, FL), Guenther; Sven (Coralville, IA), Mickle; Christal (Celebration, FL), Chi; Guochen (Coralville, IA), Kanski; Jaroslaw (Blacksburg, VA), Martin; Andrea K. (Fincastle, VA), Bera; Bindu (Blacksburg, VA)
Assignee:	KemPharm, Inc. (Coralville, IA)
Application Number:	14/557,570
Patent Claims:	1. A composition comprising acetaminophen and a conjugate, wherein the conjugate is benzoate-hydrocodone (Bz-HC) having the following structure: ##STR00025## 2. The composition of claim 1, wherein the conjugate is used to treat narcotic or opioid abuse; to reduce narcotic or opioid withdrawal; to treat moderate to severe pain; to reduce oral, intranasal or intravenous drug abuse; or to provide oral, intranasal or parenteral drug abuse resistance. 3. The composition of claim 1, wherein the conjugate exhibits an improved AUC and rate of release over time when compared to unconjugated hydrocodone over the same time period; exhibits less variability in the oral PK profile when compared to unconjugated hydrocodone; or has reduced side effects when compared with unconjugated hydrocodone. 4. The composition of claim 1, wherein the conjugate is provided in a dosage form selected from the group consisting of: a tablet, a capsule, a caplet, a suppository, a troche, a lozenge, an oral powder, a solution, an oral film, a thin strip, a slurry, and a suspension. 5. The composition of claim 1, wherein the conjugate is provided in an amount sufficient to provide a therapeutically bioequivalent AUC when compared to unconjugated hydrocodone. 6. The composition of claim 1, wherein the conjugate is provided in an amount sufficient to provide a therapeutically bioequivalent AUC and C.sub.max when compared to an equivalent molar amount of unconjugated hydrocodone. 7. The composition of claim 1, wherein the conjugate is provided in an amount sufficient to provide a therapeutically bioequivalent AUC and a lower C.sub.max when compared to an equivalent molar amount of unconjugated hydrocodone. 8. The composition of claim 1, wherein the conjugate is a salt. 9. The composition of claim 8, wherein the salt is a hydrochloride/chloride. 10. The composition of claim 1, further comprising a biologically acceptable carrier. 11. The composition of claim 1, wherein upon administration, active hydrocodone is released from the conjugate through first-pass metabolism. 12. A method for treating pain in an individual in need thereof comprising the step of orally administering a pharmaceutically effective amount of a composition comprising acetaminophen and a conjugate, wherein the conjugate is benzoate-hydrocodone (Bz-HC) having the following structure: ##STR00026## 13. The method of claim 12, wherein the conjugate exhibits an improved AUC and rate of release over time when compared to unconjugated hydrocodone over the same time period; exhibits less variability in the oral PK profile when compared to unconjugated hydrocodone; or has reduced side effects when compared with unconjugated hydrocodone. 14. The method of claim 12, wherein the composition is provided in a dosage form selected from the group consisting of: a tablet, a capsule, a caplet, a suppository, a troche, a lozenge, an oral powder, a solution, an oral film, a strip, a slurry, and a suspension. 15. The method of claim 12, wherein the conjugate is provided in an amount sufficient to provide a therapeutically bioequivalent AUC when compared to unconjugated hydrocodone. 16. The method of claim 12, wherein the conjugate is provided in an amount sufficient to provide a therapeutically bioequivalent AUC and C.sub.max when compared to an equivalent molar amount of unconjugated hydrocodone. 17. The method of claim 12, wherein the conjugate is provided in an amount sufficient to provide a therapeutically bioequivalent AUC and a lower C.sub.max when compared to an equivalent molar amount of unconjugated hydrocodone. 18. The method of claim 12, wherein the composition is used for treating pain mediated by binding of an opioid primarily to .mu. opioid receptors of the patient. 19. The method of claim 18, wherein the conjugate binds reversibly to the .mu. opioid receptors of the patient. 20. The method of claim 18, wherein the conjugate binds reversibly to the .mu. opioid receptors of the patient without a CNS depressive effect. 21. The method of claim 12, wherein the composition also reduces narcotic or opioid abuse. 22. The method of claim 12, wherein the composition also reduces narcotic or opioid withdrawal. 23. The method of claim 12, wherein the composition also reduces oral, intranasal or intravenous narcotic or opioid abuse. 24. The method of claim 12, wherein the composition also provides oral, intranasal or parenteral non corticoid opioid abuse resistance. 25. A pharmaceutical kit comprising a specified amount of individual doses in a package containing a pharmaceutically effective amount of acetaminophen and a conjugate, wherein the conjugate is benzoate-hydrocodone (Bz-HC) having the following structure: ##STR00027## 26. The pharmaceutical kit of claim 25, wherein the kit further comprises instructions for use of the kit in a method for treating pain. 27. The pharmaceutical kit of claim 25, wherein the kit further comprises instructions for use of the kit in a method for treating narcotic or opioid withdrawal symptoms. 28. The pharmaceutical kit of claim 25, wherein the kit further comprises instructions for use of the kit in a method for reducing narcotic or opioid abuse. 29. The pharmaceutical kit of claim 25, wherein the specified amount of individual doses comprise from about 1 to about 100 individual dosages. 30. The pharmaceutical kit of claim 25, wherein the individual doses comprise at least about 0.5 mg of the conjugate.