CNS pharmaceutical compositions and methods of use

• US 8,729,070 B2
• Filed: 08/20/2010
• Issued: 05/20/2014
• Est. Priority Date: 02/20/2008
• Status: Expired due to Fees

• Current Assignee: Targia Pharmaceuticals
• Original Assignee: Targia Pharmaceuticals
• Inventors: Glozman, Sabina
• Primary Examiner(s): Padmanabhan, Sreeni
• Assistant Examiner(s): Ivanova, Svetlana M
• Application Number:
  US12/860,846
• Publication Number:
  US 20110054038A1
• Time in Patent Office: 1,369 Days
• Field of Search: None
• US Class Current: 514/220
• CPC Class Codes: A61K 31/09 having two or more such linkages
• CPC Class Codes: A61K 31/138 Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine atenolol A61K31/165; pindolol A61K31/404; timolol A61K31/5377
• CPC Class Codes: A61P 25/00 Drugs for disorders of the nervous system

Abstract

The present invention is directed to CNS pharmaceutical compositions and methods of use. The pharmaceutical compositions comprise a CNS active agent and preferably at least two vagal neuromodulators, one of which is a mechanoreceptor stimulator. The vagal neuromodulators are preferably in an amount sufficient to reduce a somnolence side-effect of the CNS active agent without changing its therapeutic efficacy/activity. The invention further encompasses a method of reducing CNS active agent side-effects. The method typically comprises oral administration of at least one CNS active agent to a patient at the conventionally accepted dose; and administration of at least two vagal neuromodulators to the patient so that at least one neuromodulator is administered or released from dosage form after the CNS active agent is administered and/or released.

Claims

1. A method of reducing a side-effect of a central nervous system (CNS) active agent, the method comprising the steps of:

orally administering to a subject at least one CNS active agent at an effective dose wherein the at least one CNS active agent is selected from the group consisting of a benzodiazepine and an anti-psychotic; and

administering to the subject pseudoephedrine (PSE) and guaifenesin (GUA) in an amount sufficient to reduce a side-effect associated with the CNS active agent, wherein the side-effect is selected from the group consisting of sedation and somnolence.

2. The method of claim 1, wherein the CNS active agent has a time to maximum concentration (Tmax) and the GUA has a Tmax, and administration or release of the GUA is delayed for an amount of time being equal to the Tmax of the CNS active agent minus the Tmax of the GUA plus about 5 to about 45 minutes.

3. The method of claim 2, wherein the GUA is administered about 5 to about 30 minutes after administration of the CNS active agent.

4. The method of claim 1, wherein the side-effect is reduced without reducing the relevant therapeutic efficacy of the CNS active agent or the effective dose of the CNS active agent.