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In an exemplary embodiment, the invention is direct to a composition comprising a central nervous system (CNS) active agent and at least two vagal neuromodulators, wherein the CNS active agent has a time to maximum concentration (Tmax) and the at least two vagal neuromodulators each have a Tmax, wherein the Tmax of the CNS active agent is greater than the Tmax of at least one vagal neuromodulator and the release of at least one vagal neuromodulator is delayed, the delay being equal to the Tmax of the CNS active agent minus the Tmax of the neuromodulator plus about 5 to about 30 minutes.
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In one embodiment, the pharmaceutical composition of the present invention is formulated as a single dosage form comprising multiple beads contained in hard or soft gelatin capsules.
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The method of administering the pharmaceutical composition of the present invention may be used to treat a variety of diseases, illnesses and conditions for which the CNS active agents of the present invention might be prescribed when used alone, or in combination with other therapies.
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Thus, certain embodiments also provide pharmaceutical compositions comprising one or more compounds disclosed herein together with a pharmaceutically acceptable carrier, as well as methods of making and using the compounds and compositions.
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For example, the formulation of this embodiment may comprise GUA and PSE, wherein the GUA is released between about 10 and about 20 minutes after the CNS active agent.
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