No Abuse Potential of Silexan in Healthy Recreational Drug Users: A Randomized Controlled Trial

Author:

Seifritz Erich1,Möller Hans-Jürgen2,Volz Hans-Peter3,Müller Walter E4,Hopyan Talar5,Wacker Anna6,Schläfke Sandra6,Kasper Siegfried7

Affiliation:

1. Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zürich, Switzerland

2. Clinic and Policlinic for Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany

3. Hospital for Psychiatry, Psychotherapy and Psychosomatic Medicine Schloss Werneck, Werneck, Germany

4. Department of Pharmacology, Biocenter Goethe-University, Frankfurt, Germany

5. Scientific Affairs-Neuropsychology | Early Phase; Syneos Health, Toronto, Canada

6. Dr. Willmar Schwabe GmbH & Co. KG, Karlsruhe, Germany

7. Center for Brain Research, Medical University of Vienna, Vienna, Austria

Abstract

Abstract Background Silexan is a lavender essential oil with established anxiolytic and calming efficacy. Here we asked whether there is a potential for abuse in human patients. Methods We carried out a phase I abuse liability single-center, double-blind, 5-way crossover study in healthy users of recreational central nervous system depressants. They received single oral doses of 80 mg (therapeutic dose) and 640 mg Silexan, 2 mg and 4 mg lorazepam (active control) and placebo in randomized order, with 4- to 14-day washout periods between treatments. Pharmacodynamic measures included validated visual analogue scales assessing positive, negative, and sedative drug effects and balance of effects; a short form of the Addiction Research Center Inventory; and a drug similarity assessment. The primary outcome measure was the individual maximum value on the drug liking visual analogue scale during 24 hours post-dose. Results Forty participants were randomized and 34 were evaluable for pharmacodynamic outcomes. In intraindividual head-to-head comparisons of the drug liking visual analogue scale maximum value, both doses of Silexan were rated similar to placebo whereas differences were observed between Silexan and lorazepam and between placebo and lorazepam (P < .001). These data were supported by all secondary measures of positive drug effects and of balance of effects. Differences between placebo and both doses of Silexan were always negligible in magnitude. Moreover, Silexan showed no sedative effects and was not perceived to be similar to commonly used drugs that participants had used in the past. Conclusions Silexan did not exhibit any abuse potential in a standard abuse potential detection screen study and is unlikely to be recreationally abused.

Funder

Dr. Willmar Schwabe GmbH & Co. KG

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

Reference38 articles.

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