Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 1987;93(3):296-300.
doi: 10.1007/BF00187246.

Suriclone and diazepam in the treatment of neurotic anxiety. A double-blind cross-over trial

Affiliations
Clinical Trial

Suriclone and diazepam in the treatment of neurotic anxiety. A double-blind cross-over trial

J Gerlach et al. Psychopharmacology (Berl). 1987.

Abstract

Suriclone is a new anxiolytic drug belonging to the family of cyclopyrrolones. Although chemically entirely different from the benzodiazepines, it acts as a benzodiazepine agonist with very high affinity for the benzodiazepine receptors. In the present cross-over study, 33 out-patients with a diagnosis of neurotic anxiety were treated with suriclone (mean dose 2 mg/day) and diazepam (25 mg/day) in two 6-week periods. Both drugs had a significant anxiolytic effect, but diazepam appeared to have a better effect within the first 2 weeks of treatment, while no significant difference was seen after treatment, while no significant difference was seen after treatment for 6 weeks. Suriclone and diazepam had a different side effect profile: suriclone produced mainly dizziness, while diazepam caused sedation. This may reflect the fact that suriclone and benzodiazepines bind to distinct sites or different allosteric conformations of the benzodiazepine receptors.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Life Sci. 1979 Jun 25;24(26):2417-20 - PubMed
    1. Life Sci. 1985 Jun 10;36(23 ):2247-55 - PubMed
    1. Mol Pharmacol. 1984 Nov;26(3):458-69 - PubMed
    1. Br J Med Psychol. 1959;32(1):50-5 - PubMed
    1. J Neurochem. 1983 Mar;40(3):601-7 - PubMed

Publication types