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The single dose pharmacokinetics and safety of deramciclane in healthy male volunteers
Author(s) -
Kanerva Harri,
Kilkku Olavi,
Hein Esa,
Helminen Antti,
Rouru Juha,
Tarpila Simo,
Scheinin Mika,
Huupponen Risto,
Klebovich Imre,
Drabant Sandor,
Urtti Arto
Publication year - 1999
Publication title -
biopharmaceutics and drug disposition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 58
eISSN - 1099-081X
pISSN - 0142-2782
DOI - 10.1002/(sici)1099-081x(199910)20:7<327::aid-bdd192>3.0.co;2-8
Subject(s) - pharmacokinetics , pharmacology , metabolite , tolerability , active metabolite , desmethyl , placebo , medicine , half life , crossover study , dose–response relationship , chemistry , adverse effect , alternative medicine , pathology
The pharmacokinetics and tolerability of a new putative non‐benzodiazepine type anxiolytic compound deramciclane was studied in two consecutive studies. An open dose‐escalation design was used to study doses from 0.2 to 50 mg in 18 healthy male volunteers. In the second study doses from 50 to 150 mg were investigated in 14 healthy males in a double‐blind, placebo‐controlled, dose escalation study. Deramciclane was rapidly absorbed from the GI‐tract and T max was 2–4 h. The elimination half‐life increased from about 20 h to about 32 h with the increasing dose. Nevertheless, the AUC 0–∞ values increased linearly within the studies over the dose ranges of 3–50 and 50–150 mg. However, the increase was more than the ratio of the dose over the total dose range of 3–150 mg. Therefore, non‐linear pharmacokinetics of deramciclane at high doses cannot be excluded. N ‐desmethyl deramciclane, which is the active metabolite of deramciclane, was determined in plasma. C max was reached at about 6 h. The AUC 0–48 h for the N ‐desmethyl metabolite was about one third of the AUC 0–∞ of the parent compound and the ratio remained constant at each dose level. Deramciclane was safe, and was well tolerated at each dose level. Copyright © 1999 John Wiley & Sons, Ltd.