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BPL-003 Efficacy and Safety in Treatment Resistant Depression

Treatment Resistant Depression Clinical Trial

Official title:
A Quadruple Masked, Dose-Finding Study to Evaluate the Efficacy and Safety of Intranasal BPL-003 in Patients With Treatment Resistant Depression

Clinical Trial Summary

This is a Phase 2 study randomized, quadruple masked, multi-center study designed to investigate the efficacy and safety of a single dose of BPL-003 combined with psychological support in patients with treatment resistant depression (TRD).

Clinical Trial Description

Approximately 225 eligible participants will be receive a single dose of either low, medium, or high doses BPL-003, given intranasally, with 8 weeks of follow-up assessments. Psychological support will be given before, during and after dosing. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05870540
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 September 14, 2023
Completion date December 2024
View Details
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