US2021100817A1PendingUtilityA1

Anticonvulsant activity of steroids

Assignee: UNIV CALIFORNIAPriority: Nov 30, 2012Filed: Oct 6, 2020Published: Apr 8, 2021
Est. expiryNov 30, 2032(~6.3 yrs left)· nominal 20-yr term from priority
A61P 25/28A61P 25/34A61K 9/08A61K 31/57A61K 31/56A61K 47/40A61P 25/08A61K 9/0019A61P 25/22A61P 25/32A61K 31/573A61P 25/24A61P 25/00
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Claims

Abstract

The present invention relates to methods of preventing, inhibiting, delaying, and/or mitigating seizures by administration of a steroid, e.g., a neurosteroid, e.g., allopregnanolone.

Claims

exact text as granted — not AI-modified
1 . A method of treating, reducing, and/or mitigating symptoms associated with and/or caused by traumatic brain injury, Alzheimer's disease, epilepsy, anxiety, fragile X syndrome, post-traumatic stress disorder, lysosomal storage disorders (Niemann-Pick type C disease), depression (including post-partum depression), premenstrual dysphoric disorder, alcohol craving, and smoking cessation in a subject in need thereof, comprising administration to the subject a steroid. 
     
     
         2 . (canceled) 
     
     
         3 . A method of accelerating the termination or abortion of an impending seizure in a subject in need thereof, comprising administration to the subject a steroid. 
     
     
         4 . The method of  claim 1 , wherein the steroid is a neurosteroid. 
     
     
         5 . The method of  claim 1 , wherein the neurosteroid is selected from the group consisting of allopregnanolone, allotetrahydrodeoxycorticosterone, ganaxolone, alphaxolone, alphadolone, hydroxydione, minaxolone, and Althesin. 
     
     
         6 . The method of  claim 5 , wherein the neurosteroid is allopregnanolone. 
     
     
         7 . The method of  claim 4 , wherein the steroid is formulated in a cyclodextrin, wherein the cyclodextrin is hydroxypropyl-beta-cyclodextrin, sulfobutylether-beta-cyclodextrin sodium salt, or a mixture thereof. 
     
     
         8 . (canceled) 
     
     
         9 . The method of  claim 1 , wherein the subject is experiencing aura. 
     
     
         10 . The method of  claim 1 , wherein the subject has been warned of an impending seizure. 
     
     
         11 . The method of  claim 1 , wherein the subject is experiencing a seizure. 
     
     
         12 . The method of  claim 1 , wherein the subject has status epilepticus. 
     
     
         13 . The method of  claim 1 , wherein the subject has myoclonic epilepsy. 
     
     
         14 . The method of  claim 1 , wherein the subject suffers from seizure clusters. 
     
     
         15 . The method of  claim 1 , wherein the seizure is a tonic seizure. 
     
     
         16 . The method of  claim 1 , wherein the seizure is a clonic seizure. 
     
     
         17 . The method of  claim 1 , wherein the subject is a human. 
     
     
         18 . The method of  claim 1 , wherein the steroid is administered intramuscularly (i.m.), subcutaneously (s.c.) or intravenously (i.v.). 
     
     
         19 . The method of  claim 1 , wherein the steroid is administered at a dose in the range of about 0.25 mg/kg to about 15 mg/kg. 
     
     
         20 . The method of  claim 1 , comprising treating, reducing, and/or mitigating symptoms associated with and/or caused by epilepsy by intramuscularly (i.m.), subcutaneously (s.c.) or intravenously (i.v.) administering allopregnanolone formulated in a sulfobutylether-beta-cyclodextrin sodium salt. 
     
     
         21 - 28 . (canceled)

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