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Daytime pharmacodynamic and pharmacokinetic evaluation of low‐dose sublingual transmucosal zolpidem hemitartrate
Author(s) -
Roth Thomas,
Mayleben David,
Corser Bruce C.,
Singh Nikhilesh N.
Publication year - 2008
Publication title -
human psychopharmacology: clinical and experimental
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 78
eISSN - 1099-1077
pISSN - 0885-6222
DOI - 10.1002/hup.884
Subject(s) - zolpidem , sedation , pharmacodynamics , pharmacokinetics , medicine , digit symbol substitution test , dosing , anesthesia , sedative , pharmacology , placebo , hypnotic , insomnia , alternative medicine , pathology
Objectives Buffered low‐dose sublingual transmucosal zolpidem lozenge hemitartrate (ST zolpidem) is being developed for the treatment of middle‐of‐the‐night insomnia. The objective of this double‐blind placebo‐controlled cross‐over study ( n  = 24) was to evaluate the pharmacokinetics (PK) and daytime‐sedative profile of 1.0, 1.75, and 3.5 mg dose of the formulation. Methods Daytime sedation was measured pre‐dose and up to 5 h post‐dose objectively by the Digit Symbol Substitution Test (DSST) and subjectively using the Visual Analog Scale (VAS). Blood samples for PK assessment was collected pre‐dose and up to 12 h post‐dose. Results The 1.75 and 3.5 mg, but not the 1 mg, ST zolpidem produced significant sedation versus placebo within 20 min of dosing which lasted for up to 3 h. Zolpidem from the formulation was rapidly absorbed and reached maximum plasma concentrations within 38 min of dosing, however the half‐life was independent of the dose and side effects were consistent with the known pharmacology of the drug. Conclusions ST zolpidem produced rapid, short duration of sedation and the effect was consistent with its PK profile. This novel low‐dose formulation of zolpidem may provide clinicians and patients with a prn option for the management of sleep maintenance insomnia. Copyright © 2007 John Wiley & Sons, Ltd.

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