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Clinical Trial ● Currently Recruiting Phase II NCT05660642

An Open-Label Study to Evaluate the Safety, Tolerability and Pharmacodynamics of BPL-003 in Patients With Treatment Resistant Depression

An Open-Label Study to Evaluate the Safety, Tolerability and Pharmacodynamics of BPL-003 in Patients With Treatment Resistant Depression — Recruiting • Phase II • Mental Health / Psychiatry…

📅 26 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT05660642
Start
2023-02-10
Completion
2026-11
ClinicaliQ Trial Snapshot
  • An Open-Label Study to Evaluate the Safety, Tolerability and Pharmacodynamics of BPL-003 in Patients With Treatment Resistant Depression — Recruiting • Phase II • Mental Health / Psychiatry • NCT05660642.
  • BPL-003 Trial Summary.
  • Intranasal BPL-003 with psychological support tested for safety and effectiveness in treatment-resistant depression, used alone or with SSRIs.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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What This Trial Is Studying

An open-label, multi-centre, Phase 2a study to evaluate the safety, tolerability, and pharmacodynamics of one and two doses of intranasal BPL-003 combined with psychological support, in patients with treatment resistant depression when administered as monotherapy or as adjunctive therapy with defined SSRIs (citalopram, escitalopram, sertraline or fluoxetine). Conditions: Treatment Resistant Depression Interventions: BPL-003 Lead Sponsor: Beckley Psytech Limited Planned Enrollment: 64 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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