IP Library Granted Patent US 8,835,439
Granted Patent B2
US 8,835,439 · App. 13/768,641 · Granted Sep 16, 2014

Pharmaceutical composition containing (2R)-methyl-1-3-[2-(3-pyridinyloxy)ethoxy]-2-pyrazinylpiperazine L-malate for treatment of serotonin-related diseases

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Quick Facts
Patent No.
US 8,835,439
App. No.
13/768,641
Granted
Sep 16, 2014
Kind
B2
Abstract

The present invention relates to a process for the preparation of compounds which are therapeutically active in the central nervous system. In one aspect, the invention relates to a process for the preparation of compounds of the general formula (I): wherein HA is a pharmaceutically acceptable acid and R 1 -R 4 are each independently selected from the group consisting of hydrogen, halogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, and di-C 1 -C 6 -alkylamino-C 2 -C 6 -alkoxy. The invention also relates to the use of said compound to manufacture a medicament for the treatment of a serotonin-related disorder.

Claims (12)

1. A pharmaceutical composition comprising:

a compound of formula (I)

wherein R 1 , R 2 , R 3 , and R 4 are independently hydrogen and HA is L-malic acid, and a pharmaceutically acceptable carrier.

2. The pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable carrier is water, gelatin, gum arabicum, lactose, microcrystalline cellulose, starch, sodium starch glycolate, calcium hydrogen phosphate, magnesium stearate, talcum, colloidal silicon dioxide, or a combination thereof.

3. The pharmaceutical composition of claim 2 , further comprising a stabilizer, wetting agent, emulsifier, flavoring agent, buffer, or combination thereof.

4. The pharmaceutical composition of claim 2 , wherein the composition is formulated for oral administration.

5. The pharmaceutical composition of claim 2 , wherein the composition is formulated for parenteral administration.

6. The pharmaceutical composition of claim 2 , wherein the composition is formulated for transdermal administration.

7. The pharmaceutical composition of claim 2 , wherein the composition is formulated as a solid dosage form.

8. The pharmaceutical composition of claim 2 , wherein the composition is formulated as a liquid dosage form.

9. The pharmaceutical composition of claim 2 , wherein the composition is formulated as a suspension.

10. The pharmaceutical composition of claim 2 , wherein the composition is formulated as an emulsion.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 2, 2014
From: BIOVITRUM AB (PUBL)
To: PROXIMAGEN NEUROSCIENCE PLC
Reel/Frame 031873/0532 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 2, 2014
From: PROXIMAGEN NEUROSCIENCE PLC
To: PROXIMAGEN LIMITED
Reel/Frame 031875/0869 →
CHANGE OF NAME Recorded Jan 2, 2014
From: BIOVITRUM AB
To: BIOVITRUM AB (PUBL)
Reel/Frame 031911/0281 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 22, 2013
From: PROXIMAGEN NEUROSCIENCE PLC
To: PROXIMAGEN LIMITED
Reel/Frame 031654/0986 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2013
From: FLECK (DECEASED), TOM; CERNERUD, MAGNUS; LUNDSTROM, HELENA; LOFSTROM, CLAES; PELCMAN, MARGIT; PAPTCHIKHINE, ALEXANDER; ANDERSSON, EMMA; NYGREN, ALF
To: BIOVITRUM AB
Reel/Frame 031430/0255 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2013
From: BIOVITRUM AB (PUBL)
To: PROXIMAGEN NEUROSCIENCE PLC
Reel/Frame 031430/0310 →