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The trial participants are expected to be enrolled over 18 months and will be followed for an average of two years.
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Compound 9 is treated with an appropriate hydroxide base, such as lithium hydroxide, in an appropriate solvent, such as a mixture of tetrahydrofuran and water, at an elevated temperature to give compound 10.
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When "alkyl" is used in one instance and a specific term such as "alkylalcohol" is used in another, it is not meant to imply that the term "alkyl" does not also refer to specific terms such as "alkylalcoliol" and the like.
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The term “sulfoxide” as used herein is represented by the formula A 1S(O)A 2, where A 1 and A 2 can be, independently, an alkyl, halogenated alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocycloalkyl, or heterocycloalkenyl group described above.
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HF, HCl, HBr, or HI) or by treating a halogenated compound with a nucleophile such as an amine.
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13 Pharmacologic therapies include carbamazepine, baclofen, and benzodiazepines, but these treatments have limited efficacy.
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One or more kinds of anions with a desired property(ies) that is similar or different to that of the cation(s) can likewise be provided.
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In one embodiment, CNS active agent particles, and particles from at least two vagal neuromodulators are formulated in a single solid dosage form, such as multi-layered tablets, suspension tablets, effervescent tablets, powder, pellets, granules or capsules comprising multiple beads.
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The present invention is directed to CNS pharmaceutical compositions and methods of use.
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CNS) active agent, the method comprising: administering a CNS active agent; and administering to the patient at least two vagal neuromodulators comprising at least one mechanoreceptor stimulator, wherein the at least two vagal neuromodulators are in an amount sufficient to reduce the side-effect associated with the CNS active agent.
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