IP Library Granted Patent US 9,744,166
Granted Patent B2
US 9,744,166 · App. 15/043,167 · Granted Aug 29, 2017

Therapeutic uses of compounds having combined SERT, 5-HT

Inventors: Nicholas Moore (Ridgewood, NJ); Marianne Dragheim (Vedbæk, DK)
Assignee: H. Lundbeck A/S
A61K31/495
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Quick Facts
Patent No.
US 9,744,166
App. No.
15/043,167
Granted
Aug 29, 2017
Kind
B2
Abstract

New pharmaceutical uses of 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]piperazine and pharmaceutically acceptable salts thereof are provided.

Claims (10)

1. A method of treating mild cognitive impairment, the method comprising administering to a patient in need thereof a therapeutically effective amount of compound I, which is 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]piperazine, or a pharmaceutically acceptable salt thereof;

wherein the patient is diagnosed with mild cognitive disorder.

2. The method according to claim 1 , wherein said patient is administered the hydrobromic acid salt of 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]piperazine.

3. The method according to claim 1 , wherein said salt is crystalline and said crystalline salt is characterized by XRPD patterns as shown in any of FIGS. 1-5 .

4. The method according to claim 2 , wherein said salt is characterised by having major XRDP peaks at 6.89, 9.73, 13.78 and 14.62 (° 2θ), all ±0.1 (° 2θ).

5. The method according to claim 4 , wherein said salt is characterised by an XRDP as depicted in FIG. 3 .

6. The method according to claim 1 , wherein compound I is administered to the patient in unit doses of about 1-50 mg.

7. The method according to claim 6 , wherein the patient is administered between about 1 and 20 mg per day of the hydrobromic acid salt of 1-[2-(2,4-dimethylphenyl-sulfanyl)phenyl]piperazine orally.

8. The method according to claim 1 , wherein said patient is administered a therapeutically effective amount of compound I provided it is not the free base of 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]piperazine in a non-crystalline form.

9. The method according to claim 1 , wherein said patient has previously received medication or is still receiving medication for the treatment of said disease, the medication is ceased or reduced or has to be ceased or reduced due to sleep or sexually related adverse events.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2017
From: TAKEDA PHARMACEUTICALS U.S.A., INC
To: H. LUNDBECK A/S
Reel/Frame 043094/0134 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2017
From: MOORE, NICHOLAS; DRAGHEIM, MARIANNE
To: H. LUNDBECK A/S
Reel/Frame 043327/0784 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2017
From: BATRA, ANEIL; CHON, JIN
To: TAKEDA PHARMACEUTICALS NORTH AMERICA, INC.
Reel/Frame 043328/0168 →
CHANGE OF NAME Recorded Jul 25, 2017
From: TAKEDA PHARMACEUTICALS NORTH AMERICA, INC.
To: TAKEDA PHARMACEUTICALS U.S.A., INC.
Reel/Frame 043328/0208 →
Priority Claims (3)
DK 200701607 · Nov 13, 2007 · national
DK 200701788 · Dec 14, 2007 · national
DK 200801300 · Sep 17, 2008 · national
Continuity (5)
Continuation 12741780
Provisional Application 60987710 · Nov 13, 2007
Provisional Application 61013722 · Dec 14, 2007
Provisional Application 61097840 · Sep 17, 2008
Related Publication 20160228430A1 · Aug 11, 2016