IP Library Granted Patent US 7,022,329
Granted Patent B2
US 7,022,329 · App. 10/082,691 · Granted Apr 4, 2006

Method for treating neurogenic inflammation pain with botulinum toxin and substance P components

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Quick Facts
Patent No.
US 7,022,329
App. No.
10/082,691
Granted
Apr 4, 2006
Kind
B2
Abstract

The present invention relates to methods for treating neurogenic inflammation pain. The methods include administering an effective amount of a composition which includes a botulinum toxin component and a substance P component to a patient, thereby treating the neurogenic inflammation pain.

Claims (14)

1. A method for treating neurogenic inflammation pain, the method comprises injecting a therapeutically effective amount of about 0.01 units to about 1,000 units of an agent to a patient, the agent comprising the light chain of a botulinum toxin covalently coupled to the H N portion of the heavy chain of the botulinum toxin, and a substance P component covalently coupled to the botulinum toxin H N portion, the substance P component being effective in binding to a substance P receptor, thereby treating the neurogenic inflammation pain for at least about two months.

2. The method of claim 1 wherein the botulinum toxin light chain is the light chain of a botulinum toxin selected from the group consisting of botulinum toxin serotype A, serotype B, serotype C, serotype D, serotype E, serotype F and serotype G.

3. The method of claim 1 wherein the botulinum toxin H N portion is the H N portion of a botulinum toxin selected from the group consisting of botulinum toxin serotype A, serotype B, serotype C, serotype D, serotype E, serotype F and serotype G.

4. The method of claim 2 wherein the light chain is a light chain of a botulinum toxin serotype A.

5. The method of claim 3 wherein the H N portion is an H N portion of a botulinum toxin serotype A.

6. The method of claim 1 wherein the substance P component is substance P.

7. The method of claim 1 wherein the pain is arthritis pain.

8. The method of claim 1 wherein the agent is injected subcutaneously.

9. The method of claim 1 wherein the agent is injected intramuscularly.

10. The method of claim 1 wherein the agent is injected in an amount from about 10 −2 U/kg to about 100 U/kg.

11. The method of claim 1 wherein the agent is injected in an amount from about 10 −1 U/kg to about 10 U/kg.

12. The method of claim 1 wherein the agent is injected in an amount from about 1 unit to about 20 units.

13. The method of claim 1 wherein the agent is injected in an amount from about 1 unit to about 10 units.

14. The method of claim 1 wherein the agent is injected in an amount from about 0.1 U/kg to about 30 U/kg.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2003
From: ALLERGAN SALES, INC. (MERGED INTO ALLERGAN SALES, LLC 6/3/2002)
To: ALLERGAN, INC.
Reel/Frame 013898/0170 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2002
From: DONOVAN, STEPHEN
To: ALLERGAN SALES, INC.
Reel/Frame 012677/0707 →