IP Library Granted Patent US 10,662,146
Granted Patent B2
US 10,662,146 · App. 15/758,466 · Granted May 26, 2020

Prodrugs of fencamfamine

Inventors: Sandeep Patil (Menlo Park, CA); Ron Bihovsky (Wynnewood, PA); Steven A. Smith (San Jose, CA); Yuhua Ji (Palo Alto, CA); Valentino Stella (Lawrence, KS); Daniel D. Long (San Francisco, CA); Daniel Marquess (Half Moon Bay, CA)
Assignee: PRAXIS BIORESEARCH, LLC
C07C237/04A61K9/0019A61K9/0053A61K9/0095A61K47/10A61K47/26A61K47/38A61K47/542A61K47/64C07C233/06C07C237/20C07C237/22C07C271/24C07C271/56C07K5/06026C07K5/06052C07B2200/07C07C2602/42
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Quick Facts
Patent No.
US 10,662,146
App. No.
15/758,466
Granted
May 26, 2020
Kind
B2
Abstract

Disclosed herein are pharmaceutical compositions with fencamfamine or fencamfamine related prodrug derivatives. The pharmaceutical compositions are for targeted therapeutic applications including, but not limited to, treating cancer-related fatigue, apathy in Alzheimer's Disease, major depression, and attention deficit-hyperactivity disorder. Also disclosed are methods of synthesizing the pharmaceutical compositions with fencamfamine or fencamfamine related prodrug derivatives.

Claims (21)

1. A prodrug composition comprising at least one conjugate of N-ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine or any of its stereoisomers wherein the conjugate is of the following formula (I):

wherein Y is —C(O)X;

wherein: X is selected from the group consisting of —OR 1 , —NHR 1 , —NR 1 R 5 , —O(CR 2 R 6 )OR 3 , O(CR 2 R 6 )SR 3 , and —O(CR 2 R 6 )NR 3 ;

wherein R 1 is independently selected from optionally substituted C 1-16 alkyl, optionally substituted aryl, and optionally substituted cycloalkyl;

wherein R 2 , R 5 , and R 6 are independently selected from hydrogen, optionally substituted C 1-6 alkyl;

whererin R 3 is an optionally substituted C 12-26 alkanoyl.

2. The prodrug composition of claim 1 , wherein R 1 is selected from the group consisting of Me, Et, t Bu, 5-isopropyl-2-methylphenyl, and 2-isopropyl-5-methylphenyl.

3. The prodrug composition of claim 1 , wherein R 2 and R 6 are independently selected from the group consisting of H and Me.

4. The compound of claim 1 , wherein R 3 is from C12 to C18 in chain length.

5. The compound of claim 1 , wherein X is —O(CHR 2 )OR 3 .

6. The compound of claim 5 , wherein R 2 is independently selected from hydrogen, optionally substituted C 1-6 alkyl.

7. The compound of claim 1 , wherein the compound has the structure of:

8. The compound of claim 1 , wherein the compound has the structure of:

9. The prodrug composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.

10. The prodrug composition comprising the compound of claim 1 wherein the prodrug has an increased plasma or blood concentration of the released N-ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine when administered orally as compared to when it is administered intravenously and when the unconjugated drug is administered in equimolar amounts.

11. The prodrug composition comprising the compound of claim 1 wherein the prodrug composition is in the form comprising a tablet, a capsule, elixir, emulsion solution, suspension solution, or syrup.

12. A method for treating cancer-related fatigue comprising administering to the subject an effective amount of the compound of any one of claim 1 to a subject in need thereof.

13. The method of claim 12 , wherein the prodrug composition provides reduced ability to abuse the drug composition when compared to the unconjugated N-ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine.

14. The method of claim 12 , wherein the subject is mammalian.

15. The method of claim 12 , wherein the subject is human.

16. A method for treating Alzheimer's disease, Parkinson's disease, major depressive disorder, or attention deficit hyperactivity disorder comprising administering to the subject an effective amount of the compound of claim 1 to a subject in need thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2020
From: PATIL, SANDEEP; BIHOVSKY, RON; SMITH, STEVEN A.; JI, YUHUA; STELLA, VALENTINO
To: PRAXIS BIORESEARCH, LLC
Reel/Frame 052359/0610 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2020
From: LONG, DANIEL D; MARQUESS, DANIEL
To: THERAVANCE BIOPHARMA, INC.
Reel/Frame 052329/0271 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2020
From: THERAVANCE BIOPHARMA, INC.
To: PRAXIS BIORESEARCH, LLC
Reel/Frame 052330/0995 →
Continuity (4)
Provisional Application 62219052 · Sep 15, 2015
Provisional Application 62298267 · Feb 22, 2016
Provisional Application 62308078 · Mar 14, 2016
Related Publication 20190023650A1 · Jan 24, 2019