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Clinical Trial Summary

An open-label, Phase 2a study to evaluate the safety, tolerability, and pharmacodynamic effects of a single intranasal dose of BPL-003 combined with relapse prevention psychological support, to explore the potential effects on alcohol use and related symptoms in patients with Alcohol Use Disorder.


Clinical Trial Description

Approximately 12 eligible participants will be receive a single dose of BPL-003, given intranasally, with 12 weeks of follow-up assessments. Psychological support will be given before, during and after dosing ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05674929
Study type Interventional
Source Beckley Psytech Limited
Contact Beckley Psytech Ltd
Phone +44 (0)1865 987633
Email Medinfo@beckleypsytech.com
Status Recruiting
Phase Phase 2
Start date May 30, 2023
Completion date October 2024

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