US2001053369A1PendingUtilityA1
Epilepsy treatment
Priority: Jun 14, 2000Filed: Jul 12, 2001Published: Dec 20, 2001
Est. expiryJun 14, 2020(expired)· nominal 20-yr term from priority
Inventors:Stephen Donovan
A61P 43/00A61P 25/02A61P 25/14A61P 25/16A61P 25/00A61P 25/08A61K 38/00A61P 21/00A61K 38/4893A61P 21/02A61K 39/08Y02A50/30
53
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Methods for treating a movement disorder by intracranial administration to a human patient of a therapeutically effective amount of a neurotoxin, such as a botulinum toxin type A.
Claims
exact text as granted — not AI-modifiedI claim:
1 . A method for treating a movement disorder, the method comprising the step of intracranial administration of a neurotoxin to a patient, thereby alleviating a symptom of a movement disorder.
2 . The method of claim 1 , wherein the neurotoxin is made by a bacterium selected from the group consisting of Clostridium botulinum, Clostridium butyricum and Clostridium beratti.
3 . The method of claim 1 , wherein the neurotoxin is a botulinum toxin.
4 . The method of claim 3 , wherein the botulinum toxin is selected from the group consisting of botulinum toxin types A, B, C 1 , D, E, F and G.
5 . The method of claim 3 , wherein the botulinum toxin is botulinum toxin type A.
6 . The method of claim 3 , wherein the botulinum toxin is administered in an amount of between about 10 −3 U/kg and about 10 U/kg.
7 . The method of claim 1 , wherein the symptom alleviating effect persists for between about 1 month and about 5 years.
8 . The method of claim 1 , wherein the neurotoxin is administered to a lower brain region.
9 . The method of claim 1 , wherein the neurotoxin is administered to a pontine region
10 . The method of claim 1 , wherein the neurotoxin is administered a mesopontine region
11 . The method of claim 1 , wherein the neurotoxin is administered to a globus pallidus.
12 . The method of claim 1 wherein the neurotoxin is administered to a thalamus.
13 . The method of claim 1 , wherein the neurotoxin is a modified neurotoxin.
14 . The method of claim 13 , wherein the modified neurotoxin has at least one of its amino acids deleted, modified or replaced, as compared to a native neurotoxin.
15 . The method of claim 13 , wherein the modified neurotoxin is a recombinant produced neurotoxin or a derivative or fragment thereof.
16 . The method of claim 1 , wherein the intracranial administration step comprises implantation of controlled release botulinum toxin system.
17 . A method for treating a movement disorder, the method comprising the step of intracranial administration of a therapeutically effective amount of a botulinum toxin to a patient, thereby treating a symptom of a movement disorder.
18 . The method of claim 17 , wherein the botulinum toxin is botulinum toxin type A
19 . The method of claim 17 , wherein the movement disorder is selected from the group consisting of Parkinson's disease, Huntington's Chorea, progressive supranuclear palsy, Wilson's disease, Tourettes syndrome, epilepsy, chronic tremor, tics , dystonias and spasticity.
20 . A method for treating Parkinson's disease, the method comprising the step of intracranial administration of a therapeutically effective amount of a botulinum toxin to a patient, thereby treating a movement disorder symptom of Parkinson's disease.
21 . The method of claim 19 , wherein the botulinum toxin is botulinum toxin type A
22 . A method for treating a movement disorder, the method comprising the steps of:
(a) selecting a neurotoxin with tremor suppressant activity: (b) choosing an intracranial target tissue which influences a movement disorder; and; (c) intracranially administering to the target tissue a therapeutically effective amount of the neurotoxin selected, thereby treating the movement disorder.
23 . The method of claim 22 , wherein the neurotoxin is a botulinum toxin.Join the waitlist — get patent alerts
Track US2001053369A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.