IP Library Granted Patent US 8,557,256
Granted Patent B2
US 8,557,256 · App. 10/460,898 · Granted Oct 15, 2013

Treatment for cervical dystonia with the neurotoxic component of a botulinum toxin

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Quick Facts
Patent No.
US 8,557,256
App. No.
10/460,898
Granted
Oct 15, 2013
Kind
B2
Abstract

A method and composition for treating a patient suffering from a disease, disorder or condition and associated pain include the administration to the patient of a therapeutically effective amount of a neurotoxin selected from a group consisting of Botulinum toxin types A, B, C, D, E, F and G.

Claims (30)

1. A method for treating cervical dystonia, the method comprising the step of administering to a human patient a therapeutically effective amount of a neurotoxic component of a Botulinum toxin type B to thereby treat the patient's cervical dystonia, wherein the neurotoxic component administered to the patient has a molecular weight of about 150 kilodaltons.

2. The method of claim 1 , wherein between about 100 units and about 1000 units of the neurotoxic component is administered.

3. The method of claim 1 , wherein alleviation of the cervical dystonia occurs in about 3 to about 7 days.

4. A method for treating cervical dystonia, the method comprising the step of administering to a human patient a therapeutically effective amount of a neurotoxic component from a single Botulinum toxin type to thereby treat the patient's cervical dystonia, wherein the neurotoxic component administered to the patient has a molecular weight of about 150 kilodaltons, and wherein said Botulinum toxin is Botulinum toxin type B.

5. A method for treating cervical dystonia, the method comprising the step of administering to a human patient a therapeutically effective amount of a neurotoxic component from only a Botulinum toxin type B to thereby treat the patient's cervical dystonia, wherein the neurotoxic component administered to the patient has a molecular weight of about 150 kilodaltons.

6. The method of claim 1 , wherein between about 80 units and about 460 units of the neurotoxic component is administered.

7. The method of claim 1 , wherein the neurotoxic component is administered by intramuscular injection.

8. The method of claim 1 , wherein an alleviation of a symptom of the cervical dystonia is evident 3 to 7 days after the administration of the neurotoxic component.

9. The method of claim 4 , wherein between about 100 units and about 1000 units of the neurotoxic component is administered.

10. The method of claim 4 , wherein between about 80 units and about 460 units of the neurotoxic component is administered.

11. The method of claim 4 , wherein the neurotoxic component is administered by intramuscular injection.

12. The method of claim 4 , wherein alleviation of the cervical dystonia occurs in about 3 to about 7 days.

13. The method of claim 4 , wherein an alleviation of a symptom of the cervical dystonia is evident 3 to 7 days after the administration of the neurotoxic component.

14. The method of claim 5 , wherein between about 100 units and about 1000 units of the neurotoxic component is administered.

15. The method of claim 5 , wherein between about 80 units and about 460 units of the neurotoxic component is administered.

16. The method of claim 5 , wherein the neurotoxic component is administered by intramuscular injection.

17. The method of claim 5 , wherein alleviation of the cervical dystonia occurs in about 3 to about 7 days.

18. The method of claim 5 , wherein an alleviation of a symptom of the cervical dystonia is evident 3 to 7 days after the administration of the neurotoxic component.

19. A method for treating cervical dystonia, the method comprising the step of administering to a human patient an effective amount of a neurotoxic component of a Botulinum toxin type B, thereby reducing the severity of an abnormal head position symptom of cervical dystonia, wherein the neurotoxic component administered to the patient has a molecular weight of about 150 kilodaltons.

20. The method of claim 19 , wherein between about 100 units and about 1000 units of the neurotoxic component is administered.

21. The method of claim 19 , wherein between about 80 units and about 460 units of the neurotoxic component is administered.

22. The method of claim 19 , wherein the neurotoxic component is administered by intramuscular injection.

23. The method of claim 19 , wherein said severity is reduced in about 3 to about 7 days.

24. The method of claim 19 , wherein reduction in said severity is evident 3 to 7 days after the administration of the neurotoxic component.

25. A method for treating cervical dystonia, the method comprising the step of administering to a human patient an effective amount of a neurotoxic component of a Botulinum toxin type B, thereby reducing a neck pain symptom of cervical dystonia, wherein the neurotoxic component administered to the patient has a molecular weight of about 150 kilodaltons.

26. The method of claim 25 , wherein between about 100 units and about 1000 units of the neurotoxic component is administered.

27. The method of claim 25 , wherein between about 80 units and about 460 units of the neurotoxic component is administered.

28. The method of claim 25 , wherein the neurotoxic component is administered by intramuscular injection.

29. The method of claim 25 , wherein said symptom is reduced in about 3 to about 7 days.

30. The method of claim 25 , wherein reduction in said symptom is evident 3 to 7 days after the administration of the neurotoxic component.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2007
From: MERZ PHARMA GMBH & CO. KGAA; MERZ PHARMACEUTICALS GMBH
To: ALLERGAN, INC.
Reel/Frame 019831/0865 →