IP Library Granted Patent US 10,548,875
Granted Patent B2
US 10,548,875 · App. 16/235,120 · Granted Feb 4, 2020

Glycopyrrolate salts

Inventors: John Allan Statler (Redwood City, CA); Anthony Adrian Shaw (North Vancouver, CA); Delphine Caroline Imbert (Cupertino, CA); Jennifer Leigh Nelson (Kokomo, IN); Patricia Andres (West Lafayette, IN); Lisa Lynn McQueen (West Lafayette, IN); Stephan Xander Mattheus Boerrigter (West Lafayette, IN); Jon Gordon Selbo (West Lafayette, IN); Mark Christopher Andres (West Lafayette, IN)
Assignee: Dermira, Inc.
A61K31/40A61K9/0014A61K9/08A61K47/10A61K47/12A61K47/32A61K47/34C07D207/12
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Quick Facts
Patent No.
US 10,548,875
App. No.
16/235,120
Granted
Feb 4, 2020
Kind
B2
Abstract

Salts of glycopyrrolate, including solid forms and formulations such as topicals thereof, are disclosed. Methods of making glycopyrrolate salts, including formulations such as topicals thereof, and methods of treating hyperhidrosis with salts of glycopyrrolate, and formulations such as topicals thereof, are disclosed.

Claims (27)

1. A racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate.

2. An absorbent pad comprising a pharmaceutically acceptable solution comprising a racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and at least one pharmaceutically acceptable additive.

3. The absorbent pad of claim 2 , wherein one pharmaceutically acceptable additive is ethanol.

4. The absorbent pad of claim 2 , wherein the weight percent of said racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate in said pharmaceutically acceptable solution is between 1% and 6%; and the pH of said pharmaceutically acceptable solution is between 3.5 and 5.5.

5. The absorbent pad of claim 2 , wherein the absorbent pad comprises polypropylene.

6. The absorbent pad of claim 2 , wherein the absorbent pad is nonwoven 100% polypropylene.

7. The absorbent pad of claim 2 , wherein the absorbent pad is sealed in a pouch.

8. The absorbent pad of claim 7 , wherein the pouch is a laminate containing aluminum foil as a layer.

9. A pharmaceutically acceptable solution comprising a racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and at least one pharmaceutically acceptable additive.

10. The pharmaceutically acceptable solution of claim 9 , wherein one pharmaceutically acceptable additive is ethanol.

11. The pharmaceutically acceptable solution of claim 9 , wherein the weight percent of said racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate is between 1% and 6%; and the pH of said pharmaceutically acceptable solution is between 3.5 and 5.5.

12. A method of treating hyperhidrosis comprising topically administering a therapeutically effective amount of a pharmaceutically acceptable solution of a racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate to the skin of a mammal.

13. The method of claim 12 , wherein said mammal is human.

14. The method of claim 13 , wherein said pharmaceutically acceptable solution is applied to the axilla.

15. The method of claim 13 , wherein said pharmaceutically acceptable solution is applied to the hands.

16. The method of claim 13 , wherein said pharmaceutically acceptable solution is applied to the feet.

17. The method of claim 13 , wherein said pharmaceutically acceptable solution is applied to the groin, face, back, or abdomen.

18. The method of claim 12 , where the administration is with an absorbent pad comprising an absorbed pharmaceutically acceptable solution of a racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate.

19. The method of claim 14 , where the administration is with an absorbent pad comprising an absorbed pharmaceutically acceptable solution of a racemic mixture of (R)-3-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate and (S)-3-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidinium 4-methylbenzenesulfonate.

20. The method of claim 12 , wherein one pharmaceutically acceptable additive is ethanol.

21. The method of claim 14 , wherein one pharmaceutically acceptable additive is ethanol.

22. The method of claim 18 , wherein one pharmaceutically acceptable additive is ethanol.

23. The method of claim 22 , wherein the pharmaceutically acceptable solution comprises between about 57 and 59.5% by weight dehydrated ethanol.

24. The method of claim 22 , wherein the pH of said pharmaceutically acceptable solution is between about 4.0 and about 5.0.

25. The method of claim 22 , wherein the pH of said pharmaceutically acceptable solution is between about 4.0 and about 4.7.

26. The method of claim 22 , wherein the pH of said pharmaceutically acceptable solution is between about 4.1 and about 4.6.

27. The method of claim 22 , wherein said pharmaceutically acceptable solution is clear and colorless or pale yellow at a pH of between about 4.0 and about 5.0 at 25° C.

Assignments (4)
SECURITY INTEREST Recorded Dec 28, 2023
From: JOURNEY MEDICAL CORPORATION; JG PHARMA, INC.
To: SWK FUNDING LLC
Reel/Frame 066157/0079 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2021
From: DERMIRA, INC.
To: JOURNEY MEDICAL CORPORATION
Reel/Frame 056829/0767 →
RELEASE OF SECURITY INTEREST Recorded Feb 20, 2020
From: ATHYRIUM OPPORTUNITIES III ACQUISITION LP
To: DERMIRA, INC.
Reel/Frame 051882/0260 →
SECURITY INTEREST Recorded Aug 28, 2019
From: DERMIRA, INC.
To: ATHYRIUM OPPORTUNITIES III ACQUISITION LP
Reel/Frame 050194/0212 →
Continuity (12)
Continuation 15996353 · Jun 1, 2018
Continuation 15438636 · Feb 21, 2017
Continuation 14989995 · Jan 7, 2016
Continuation 14643553 · Mar 10, 2015
Continuation 14473537 · Aug 29, 2014
Continuation PCTUS2014019552 · Feb 28, 2014
Continuation In Part 14024480 · Sep 11, 2013
Continuation In Part 14024484 · Sep 11, 2013
Continuation 13781390 · Feb 28, 2013
Provisional Application 61770925 · Feb 28, 2013
Provisional Application 61770920 · Feb 28, 2013
Related Publication 20190133999A1 · May 9, 2019