IP Library Granted Patent US 9,629,853
Granted Patent B2
US 9,629,853 · App. 14/718,524 · Granted Apr 25, 2017

Uses of ganaxolone

Inventors: Mathew Victor Jones (Madison, WI); Chiara Cirelli (Verona, WI); Kile Patrick Mangan (Madison, WI); Aaron B. Nelson (New York, NY)
Assignee: WISCONSIN ALUMNI RESEARCH FOUNDATION
A61K31/57A61K49/0008C12Q1/68C12Q1/6883C12Q2600/106C12Q2600/156C12Q2600/158
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Quick Facts
Patent No.
US 9,629,853
App. No.
14/718,524
Granted
Apr 25, 2017
Kind
B2
Abstract

Absence epilepsy, a form of epilepsy characterized by nonconvulsive seizures, has proven to be refractive to conventional epilepsy therapies. It has been found that low doses of ganaxolone can be used to reduce absence seizures in subjects with absence epilepsy, particularly pediatric subjects. In addition, ganaxolone therapy is particularly useful in subjects with absence epilepsy characterized by a reduction in tonic inhibition. Low dose ganaxolone is also used to reduce sleep disruptions and to treat sleep disorders in subjects in need of such treatment.

Claims (6)

1. A method of treating absence epilepsy in a mammalian subject in need thereof, comprising administering ganaxolone to the mammalian subject in an amount of 0.2 to 2 mg/kg per dose, wherein the mammalian subject has been diagnosed with absence epilepsy, wherein the epilepsy is characterized by a deficit in tonic inhibition.

2. The method of claim 1 , wherein the mammalian subject has a γ2R43Q mutation in the GABA A receptor.

3. The method of claim 1 , wherein the mammalian subject is a human pediatric subject.

4. The method of claim 3 , wherein the human pediatric subject with absence epilepsy is 1 to 18 years of age, and has an average weight of 10 to 80 kg and the dose of ganaxolone is 2 to 160 mg per administration.

5. The method of claim 1 , wherein the mammalian subject suffers from nonconvulsive seizures associated with loss of consciousness, glassy-eyed staring, spike and wave EEG discharges, or a combination thereof.

6. The method of claim 1 , wherein the mammalian subject is resistant to standard antiabsence drug therapy.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 16, 2018
From: WISCONSIN ALUMNI RESEARCH FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046172/0876 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2016
From: JONES, MATHEW; NELSON, AARON; MANGAN, KILE; CIRELLI, CHIARA
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 039088/0782 →
Continuity (2)
Provisional Application 62001347 · May 21, 2014
Related Publication 20150335659A1 · Nov 26, 2015