IP Library Granted Patent US 10,456,387
Granted Patent B2
US 10,456,387 · App. 15/913,481 · Granted Oct 29, 2019

Phacetoperane for treating of attention deficit hyperactivity disorder

Inventors: Eric Konofal (Senlis, FR); Bruno Figadere (Saint Cheron, FR)
Assignee: NLS PHARMACEUTICS AG
A61K31/4458A61K31/445C07D211/22Y02P20/55
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Quick Facts
Patent No.
US 10,456,387
App. No.
15/913,481
Granted
Oct 29, 2019
Kind
B2
Abstract

The invention relates to the treatment of an attention deficit hyperactivity disorder (ADHD) with alpha-phenyl(piperidin-2-yl)methanol, or the pharmaceutically acceptable salts and esters thereof, in particular the acetate derivative, more particularly dextrophacetoperane. The invention additionally provides a method of synthesis of the (S,S) enantiomer of alpha-phenyl(piperidin-2-yl)methanol as well as a method of synthesis of dextrophacetoperane.

Claims (9)

1. A method for treating an attention deficit hyperactivity disorder (ADHD) in a human patient by at least reducing impulsivity, comprising orally administering to said patient levophacetoperane, or a pharmaceutically acceptable salt thereof, as the sole active ingredient in an amount effective to reduce impulsivity in said patient ranging from about 5 mg to about 20 mg per day.

2. The method of claim 1 , wherein the administered amount of levophacetoperane, or a pharmaceutically acceptable salt thereof, ranges from about 5 mg to about 10 mg.

3. The method of claim 2 , wherein the human is a child or an adolescent.

4. The method of claim 1 , wherein the administered amount of levophacetoperane, or a pharmaceutically acceptable salt thereof, ranges from about 10 mg to about 20 mg.

5. The method of claim 4 , wherein the human is an adolescent or an adult.

6. The method of any of claims 1 and 2 - 5 , wherein the levophacetoperane, or a pharmaceutically acceptable salt thereof, is administered as a tablet.

7. The method of claim 1 , wherein the administered amount of levophacetoperane, or a pharmaceutically acceptable salt thereof, ranges from about 5 mg to about 15 mg.

8. The method of claim 7 , wherein the human is a child or an adolescent.

9. The method of any of claims 7 - 8 , wherein the administered levophacetoperane, or a pharmaceutically acceptable salt thereof, is as a tablet.

Assignments (2)
MERGER Recorded Sep 12, 2019
From: NLS PHARMA AG
To: NLS-1 PHARMA AG
Reel/Frame 050352/0349 →
CHANGE OF NAME Recorded Sep 12, 2019
From: NLS-1 PHARMA AG
To: NLS PHARMACEUTICS AG
Reel/Frame 050352/0447 →
Priority Claims (1)
FR 11 60902 · Nov 29, 2011 · national
Continuity (2)
Continuation 14360355
Related Publication 20180214436A1 · Aug 2, 2018