IP Library Granted Patent US 7,153,514
Granted Patent B2
US 7,153,514 · App. 10/745,332 · Granted Dec 26, 2006

Use of botulinum toxin therapy for prostatic hyperplasia and related disorders

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,153,514
App. No.
10/745,332
Granted
Dec 26, 2006
Kind
B2
Abstract

The present invention relates to methods for treating neurological-urological conditions. This is accomplished by administration of at least one neurotoxin.

Claims (23)

1. A method for treating a prostatic disorder selected from the group consisting of prostatic hyperplasia, benign prostatic hyperplasia and prostatic enlargement in a patient, the method comprising the step of administering to the prostate of a patient with the prostatic disorder a botulinum toxin, thereby treating the prostatic disorder.

2. The method of claim 1 , wherein the patent is a human male.

3. The method of claim 1 , wherein the botulinum toxin is a botulinum toxin type A.

4. The method of claim 1 , wherein the botulinum toxin is administered in a pharmaceutically acceptable formulation selected from the group consisting of: a liquid, a powder, a cream, an emulsion, a suppository, a suspension, and a solution.

5. The method of claim 1 , wherein the botulinum toxin is administered in a pharmaceutically acceptable formulation selected from the group consisting of a cream, a suspension and an emulsion.

6. The method of claim 1 , wherein the botulinum toxin is administered in an injectable, pharmaceutically acceptable formulation selected from the group consisting of a liquid, a cream, an emulsion, a suspension, and a solution.

7. The method of claim 1 , wherein the botulinum toxin is injected into the prostate gland of the patient in a pharmaceutically acceptable formulation selected from the group consisting of: a liquid, a cream, an emulsion, a suspension, and a solution.

8. The method of claim 1 , wherein the botulinum toxin is administered to the prostate of the patient by a route selected from the group consisting of a single unilateral injection, serial unilateral injections and bilateral injections.

9. The method of claim 1 , wherein the botulinum toxin is injected urethroscopically into the prostate of the patient.

10. The method of claim 1 , wherein the prostatic disorder is prostatic hyperplasia.

11. The method of claim 1 , wherein the prostatic disorder is benign prostatic hyperplasia.

12. The method of claim 1 , wherein the prostatic disorder is prostatic enlargement.

13. The method of claim 1 , wherein the prostatic disorder is secondary to abacterial prostatitis or prostarodynia.

14. The method of claim 1 , wherein administration of the botulinum toxin results in shrinkage of the patients prostate.

15. A method for treating prostatic hyperplasia in a human male, the method comprising the step of administering to the prostate of a patient with the prostatic hyperplasia a botulinum toxin, thereby treating the prostatic hyperplasia.

16. The method of claim 15 , wherein the botulinum toxin is administered in a pharmaceutically acceptable formulation selected from the group consisting of: a liquid, a powder, a cream, an emulsion, a suppository, a suspension, and a solution.

17. The method of claim 15 , wherein the botulinum toxin is administered in an injectable, pharmaceutically acceptable formulation selected from the group consisting of a liquid, a cream, an emulsion, a suspension, and a solution.

18. A method for treating benign prostatic hyperplasia in a human male, the method comprising the step of administering to the prostate of a patient with the benign prostatic hyperplasia a botulinum toxin, thereby treating the benign prostatic hyperplasia.

19. The method of claim 18 , wherein the botulinum toxin is administered in a pharmaceutically acceptable formulation selected from the group consisting of: a liquid, a powder, a cream, an emulsion, a suppository, a suspension, and a solution.

20. The method of claim 18 , wherein the botulinum toxin is administered in an injectable, pharmaceutically acceptable formulation selected from the group consisting of a liquid, a cream, an emulsion, a suspension, and a solution.

21. A method for treating prostate enlargement in a human male, the method comprising the step of administering to the prostate of a patient with the prostatic enlargement a botulinum toxin, thereby treating the prostatic enlargement.

22. The method of claim 21 , wherein the botulinum toxin is administered in a pharmaceutically acceptable formulation selected from the group consisting of: a liquid, a powder, a cream, an emulsion, a suppository, a suspension and a solution.

23. The method of claim 21 , wherein the botulinum toxin is administered in an injectable, pharmaceutically acceptable formulation selected from the group consisting of a liquid, a cream, an emulsion, a suspension, and a solution.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2015
From: THE REGENTS OF THE UNIVERSITY OF COLORADO
To: ALLERGAN, INC.
Reel/Frame 036260/0570 →