IP Library › Granted Patent US 8,871,224
Granted Patent B2
US 8,871,224 · App. 13/073,741 · Granted Oct 28, 2014

Botulinum toxin therapy for skin disorders

Inventor: Eric First (Morristown, NJ)
Assignee: Allergan, Inc.
A61K38/4893
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Quick Facts
Patent No.
US 8,871,224
App. No.
13/073,741
Granted
Oct 28, 2014
Kind
B2
Abstract

Methods for treating skin disorders by local administration of a Clostridial toxin, such as a botulinum toxin, to a patient with a skin disorder.

Claims (17)

1. A method for treating a keloid in a patient in need thereof, the method comprising the step of administering a therapeutically effective amount of a botulinum toxin complex to the keloid, to thereby treat the keloid; wherein the therapeutically effective amount administered is less than an amount used to paralyze a muscle, ranging between about 10 −3 units/kg of patient weight and about 35 units/kg of patient weight, and which reduces the keloid in size by from about 20% to 100%.

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

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

4. The method of claim 1 , wherein the administration is by topical or subcutaneous administration of the botulinum toxin.

5. The method of claim 1 , wherein administration of a botulinum toxin type A is no less than about 1 to about 200 units per patient treatment session.

6. The method of claim 2 wherein administration of a botulinum toxin type B is no less than about 40 to about 2500 units per patient treatment session.

7. A method for treating a symptom associated with a keloid in a patient in need thereof, the method comprising the step of administering a therapeutically effective amount of a botulinum toxin complex to the keloid, thereby treating the symptom associated with the keloid, wherein the therapeutically effective amount administered is less than an amount used to paralyze a muscle, ranging between about 10 −3 units/kg of patient weight and about 35 units/kg of patient weight, and which reduces the keloid in size by from about 20% to 100%.

8. The method of claim 7 , wherein the botulinum toxin is selected from the group consisting of botulinum toxin types A, B, C, D, E, F and G.

9. The method of claim 7 , wherein the administration is by injection directly to the keloid.

10. The method of claim 7 , wherein the symptom is selected from the group consisting of pain, inflammation and vascularization.

11. The method of claim 7 , wherein administration is transdermal or subdermal or intradermal.

12. The method of claim 7 , wherein the administration is by a botulinum toxin implant.

13. The method of claim 7 , wherein administration of a botulinum toxin type A is no less than about 1 to about 200 units per administration site, per patient treatment session.

14. The method of claim 7 , wherein administration of a botulinum toxin type B is no less than about 40 to about 2500 units per administration site, per patient treatment session.

15. A method for treating a keloid in a patient in need thereof, the method comprising the step of administering a dose of a botulinum toxin complex type A, to the keloid of the patient; wherein the dose administered is less than an amount used to paralyze a muscle, ranging between about 10 −3 units/kg of patient weight and about 35 units/kg of patient weight, and which reduces the keloid in size by from about 20% to 100%.

16. The method of claim 15 , wherein the administration is by injection directly to the keloid.

17. The method of claim 15 , wherein the administration is by topical or subcutaneous administration of the botulinum toxin.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2011
From: FIRST, ERIC
To: ALLERGAN, INC.
Reel/Frame 026208/0376 →
Continuity (3)
Continuation In Part 12762110 · Apr 16, 2010
Continuation In Part 10731973 · Dec 9, 2003
Related Publication 20110206731A1 · Aug 25, 2011