IP Library Granted Patent US 9,566,343
Granted Patent B2
US 9,566,343 · App. 14/336,549 · Granted Feb 14, 2017

Benzoic acid, benzoic acid derivatives and heteroaryl carboxylic acid conjugates of hydromorphone, prodrugs, methods of making and use thereof

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Quick Facts
Patent No.
US 9,566,343
App. No.
14/336,549
Granted
Feb 14, 2017
Kind
B2
Abstract

The presently described technology provides compositions comprising aryl carboxylic acids chemically conjugated to hydromorphone (4,5-α-epoxy-3-hydroxy-17-methyl morphinan-6-one) to form novel prodrugs/compositions of hydromorphone. The hydromorphone prodrugs of the present technology have decreased side effects and decreased potential for abuse compared to unconjugated hydromorphone. The present technology also provides methods of treating patients, pharmaceutical kits and methods of synthesizing conjugates of the present technology.

Claims (12)

1. A composition comprising at least one conjugate, wherein the at least one conjugate is 3-aspirin-hydromorphone.

2. The composition of claim 1 , wherein the at least one conjugate is used to treat narcotic or opioid abuse; to prevent narcotic or opioid withdrawal; to treat moderate to severe pain; to reduce or prevent oral, intranasal or intravenous drug abuse; or to provide oral, intranasal or parenteral drug abuse resistance.

3. The composition of claim 2 , wherein oral administration of the at least one conjugate results in an improved rate of release over time when compared to unconjugated hydromorphone over the same time period.

4. The composition of claim 2 , wherein oral administration of the at least one conjugate results in less variability in the oral PK profile when compared to unconjugated hydromorphone.

5. The composition of claim 2 , wherein oral administration of the at least one conjugate results in reduced side effects when compared with unconjugated hydromorphone.

6. The composition of claim 5 , wherein the reduced side effect is reduced opioid induced constipation.

7. The composition of claim 1 , wherein the at least one 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.

8. The composition of claim 2 , wherein oral administration of the at least one conjugate provides a therapeutically bioequivalent AUC and/or a bioequivalent when compared to an equivalent molar amount of unconjugated hydromorphone.

9. The composition of claim 2 , wherein intranasal or intravenous administration of the at least one conjugate provides a lower AUC and/or C max when compared to an equivalent molar amount of unconjugated hydromorphone.

10. The composition of claim 2 , wherein oral administration of the at least one conjugate provides a decreased overdose potential when compared to an equivalent molar amount of unconjugated hydromorphone.

11. The composition of claim 1 , wherein the at least one conjugate provides an increased tamper resistance when compared to unconjugated hydromorphone.

12. A composition comprising 3-aspirin-hydromorphone, having the following structure:

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Mar 13, 2026
From: ALTER DOMUS (US) LLC
To: ZEVRA THERAPEUTICS, INC.
Reel/Frame 075080/0907 →
SECURITY INTEREST Recorded Apr 8, 2024
From: ZEVRA THERAPEUTICS, INC.
To: ALTER DOMUS (US) LLC
Reel/Frame 067040/0637 →
CHANGE OF NAME Recorded Feb 23, 2024
From: KEMPHARM, INC.
To: ZEVRA THERAPEUTICS, INC.
Reel/Frame 066664/0108 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 5, 2014
From: MICKLE, TRAVIS; GUENTHER, SVEN; CHI, GUOCHEN; KANSKI, JAROSLAW; MARTIN, ANDREA K.; BERA, BINDU
To: KEMPHARM, INC.
Reel/Frame 033675/0727 →