US2008160121A1PendingUtilityA1
Intracranial botulinum toxin therapy for focal epilepsy
Est. expiryJun 14, 2020(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/00A61P 25/14A61P 25/08A61P 25/02A61P 25/16A61P 21/02A61K 38/00A61P 21/00A61K 38/4893A61K 39/08Y02A50/30
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Claims
Abstract
Methods for treating and/or curing epilepsy by intracranial administration of a botulinum toxin.
Claims
exact text as granted — not AI-modified1 . A method for treating focal epilepsy in a patient in need thereof, the method comprising the steps of:
identifying an epileptogenic focus of a patient; and intracranially administering a botulinum toxin to the epileptogenic focus of the patient, thereby treating the focal epilepsy of the patient.
2 . The method of claim 1 , wherein the botulinum toxin is selected from the group consisting of botulinum toxin types A, B, C 1 , D, E, F and G.
3 . The method of claim 1 , wherein the botulinum toxin is botulinum toxin type A.
4 . The method of claim 1 , wherein the botulinum toxin is administered in an amount of between about 10 −3 U/kg and about 10 U/kg of patient weight.
5 . The method of claim 1 , wherein the method alleviates epilepsy for between about 1 month and about 5 years.
6 . The method of claim 1 , wherein the identifying step utilizes electroencephalography to determine the location of the epileptogenic focus.
7 . The method of claim 1 , wherein the botulinum toxin is administered to an epileptogenic focus at a temporal gyrus.
8 . The method of claim 1 , wherein the botulinum toxin is administered to an epileptogenic focus at a fusiform gyrus.
9 . The method of claim 1 , wherein the botulinum toxin is administered to an epileptogenic focus at a middle or superior temporal gyrus.
10 . The method of claim 1 wherein the botulinum toxin is administered to an epileptogenic focus a left or right or fusiform gyrus.
11 . The method of claim 1 wherein the botulinum toxin is administered to an epileptogenic focus at a mesial region of a temporal lobe.
12 . The method of claim 1 , wherein the intracranial administration step comprises implantation of a controlled release botulinum toxin system.
13 . A method for treating focal epilepsy in a patient in need thereof, the method comprising the step of intracranial administration of a therapeutically effective amount of a botulinum toxin type A to an epileptogenic focus of a patient, thereby treating focal epilepsy of the patient.
14 . The method of claim 13 , wherein the patient experiences intractable seizures as a result of the focal epilepsy.
15 . The method of claim 13 , wherein the botulinum toxin is administered in an amount of between about 10 −2 U/kg and about 1 U/kg of patient weight.
16 . A method for treating focal epilepsy, the comprising the step of administering intracranially a therapeutically effective amount of a botulinum toxin to an identified epileptogenic focus, wherein the identified epileptogenic focus is located in an anterior portion of the temporal lobe, thereby treating the focal epilepsy.
17 . The method of claim 16 , wherein the anterior portion is 5 to 6 cm from the tip of the temporal lobe along a middle temporal gyrus.
18 . The method of claim 16 , wherein the botulinum toxin is selected from the group consisting of botulinum toxin types A, B, C 1 , D, E, F and G.
19 . The method of claim 16 , wherein the botulinum toxin is botulinum toxin type A.
20 . The method of claim 16 , wherein the botulinum toxin is administered in an amount of between about 10 −3 U/kg and about 100 U/kg of patient weight.Join the waitlist — get patent alerts
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