IP Library Granted Patent US 11,850,244
Granted Patent B2
US 11,850,244 · App. 16/706,009 · Granted Dec 26, 2023

Drug delivery systems and methods for treatment of bladder dysfunction or disorder using trospium

Inventor: Dennis Giesing (Lee's Summit, MO)
Assignee: TARIS Biomedical LLC
A61K31/46A61K9/0034A61M31/002
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Quick Facts
Patent No.
US 11,850,244
App. No.
16/706,009
Granted
Dec 26, 2023
Kind
B2
Abstract

Methods, devices, and medicaments that include trospium are provided for use in the treatment of bladder dysfunction by locally administering the trospium into the bladder to achieve a sustained concentration of trospium in urine in the bladder sufficient to produce a therapeutic concentration of trospium in bladder tissue. The drug may be delivered into the bladder from an intravesical drug delivery device inserted into the bladder, wherein the device continuously releases the drug into the urine in the bladder over an extended period of hours or days.

Claims (40)

1. A method of reducing bladder spasms and involuntary detrusor contractions in a patient without suppressing overall bladder function, comprising:

locally administering trospium into the bladder of the patient continuously over a treatment period from 30 days to 180 days to achieve a sustained concentration of trospium in urine in the bladder sufficient to produce a therapeutic concentration of trospium in bladder tissue,

wherein the locally administering into the patient's bladder is continuous at a mean average amount of from 0.15 mg/day to 15 mg/day of the trospium for the treatment period.

2. The method of claim 1 , wherein the sustained concentration of the trospium in urine in the bladder is from 0.05 μg/ml to 100 μg/ml continuously over the treatment period.

3. The method of claim 1 , wherein the sustained concentration of the trospium in urine in the bladder is from 0.1 μg/ml to 100 μg/ml continuously over the treatment period.

4. The method of claim 1 , wherein the sustained concentration of the trospium in urine in the bladder is from 1 μg/ml to 100 μg/ml continuously over the treatment period.

5. The method of claim 1 , wherein the sustained concentration of the trospium in urine in the bladder is from 10 μg/ml to 100 μg/ml continuously over the treatment period.

6. The method of claim 1 , wherein the trospium is in the form of trospium chloride or another pharmaceutically acceptable salt of trospium.

7. The method of claim 1 , wherein the trospium is delivered into the bladder from an intravesical drug delivery device which releases the trospium into the urine in the bladder.

8. The method of claim 7 , wherein the intravesical drug delivery device comprises a housing which contains and controllably releases the trospium and is elastically deformable between a retention shape configured to retain the device in a patient's bladder and a deployment shape for passage of the device through the patient's urethra.

9. The method of claim 8 , wherein the trospium contained in the housing is in a non-liquid form.

10. The method of claim 9 , wherein the non-liquid form is selected from the group consisting of tablets, granules, semisolids, capsules, and combinations thereof.

11. The method of claim 7 , wherein the trospium is released from the intravesical drug delivery device by osmotic pressure through an aperture in the device.

12. An intravesical drug delivery device, comprising:

a housing configured for intravesical insertion; and

a dosage form comprising a pharmaceutically acceptable salt of trospium,

wherein the housing holds the dosage form and is configured to release the trospium into the bladder in an amount therapeutically effective to reduce bladder spasms and involuntary detrusor contractions in a patient without suppressing overall bladder function,

wherein the device is configured to continuously release the trospium at a mean average amount of from 0.15 mg/day to 15 mg/day over a treatment period of from 30 days to 180 days.

13. The device of claim 12 , wherein the dosage form comprises tablets comprising trospium chloride.

14. The device of claim 12 , wherein the housing is elastically deformable between a retention shape configured to retain the device in a patient's bladder and a deployment shape for passage of the device through the patient's urethra.

15. The device of claim 12 , wherein the trospium contained in the housing is in a non-liquid form.

16. The method of claim 1 , wherein the treatment period is 90 days.

17. The device of claim 12 , wherein the treatment period is 90 days.

18. The method of claim 1 , wherein the locally administering into the patient's bladder is at a mean average amount of from 1 mg/day to 15 mg/day of the trospium, and wherein the treatment period is from 30 days to 90 days.

19. The method of claim 18 , wherein the treatment period is from 60 days to 90 days.

20. The device of claim 12 , wherein the device is configured to release the trospium at a mean average amount of from 1 mg/day to 15 mg/day, and wherein the treatment period is from 30 days to 90 days.

21. The device of claim 20 , wherein the treatment period is from 60 days to 90 days.

22. A method of reducing bladder spasms and involuntary detrusor contractions in a patient without suppressing bladder function, comprising:

locally administering trospium into the bladder of the patient continuously over a treatment period from 30 days to 180 days to achieve a sustained concentration of trospium in urine in the bladder sufficient to produce a therapeutic concentration of trospium in bladder tissue,

wherein the locally administering into the patient's bladder is at a mean average amount of from 0.15 mg/day to 15 mg/day of the trospium for the treatment period, and wherein the sustained concentration of the trospium in urine in the bladder is from 0.05 μg/ml to 100 μg/ml continuously over the treatment period.

23. The method of claim 22 , wherein the locally administering into the patient's bladder is at a mean average amount of from 1 mg/day to 15 mg/day of the trospium, and wherein the treatment period is from 30 days to 90 days.

24. The method of claim 22 , wherein the trospium is delivered into the bladder from an intravesical drug delivery device which releases the trospium into the urine in the bladder.

25. An intravesical drug delivery device, comprising:

a housing configured for intravesical insertion; and

a dosage form comprising a pharmaceutically acceptable salt of trospium,

wherein the housing holds the dosage form and is configured to release the trospium into the bladder in an amount therapeutically effective to reduce bladder spasms and involuntary detrusor contractions in a patient without suppressing overall bladder function,

wherein the device is configured to release the trospium at a mean average amount of from 0.15 mg/day to 15 mg/day over a treatment period of from 30 days to 180 days, and

wherein the sustained concentration of the trospium in urine in the bladder is from 0.05 μg/ml to 100 μg/ml continuously over the treatment period.

26. The device of claim 25 , wherein the intravesical drug delivery device is configured to continuously release the trospium into the urine in the bladder over the treatment period.

27. The device of claim 25 , wherein the housing is elastically deformable between a retention shape configured to retain the device in a patient's bladder and a deployment shape for passage of the device through the patient's urethra.

Assignments (4)
MERGER Recorded Jun 1, 2026
From: TARIS BIOMEDICAL LLC
To: JANSSEN BIOTECH, INC.
Reel/Frame 074810/0895 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2019
From: GIESING, DENNIS
To: TARIS BIOMEDICAL, INC.
Reel/Frame 051216/0282 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2019
From: LIRIS BIOMEDICAL, INC.
To: TARIS BIOMEDICAL LLC
Reel/Frame 051218/0624 →
CHANGE OF NAME Recorded Dec 9, 2019
From: TARIS BIOMEDICAL, INC.
To: LIRIS BIOMEDICAL, INC.
Reel/Frame 051227/0351 →
Continuity (4)
Continuation 14658699 · Mar 16, 2015
Continuation PCTUS2013060479 · Sep 18, 2013
Provisional Application 61702576 · Sep 18, 2012
Related Publication 20200108057A1 · Apr 9, 2020