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CompletedPhase 1

Single Ascending Dose Study With BPL-003 in Healthy Subjects

NCT05347849 · Beckley Psytech Limited

Closed to entry
Status
Not accepting participants
Phase 1
Phase
62
Target enrolment
1
Study sites
Outside the US

What it is testing

Summary

The study will evaluate safety, tolerability and PK profile of BPL-003 in healthy subjects

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Percentage of subjects with treatment emergent AEs (TEAES)

    Measured over From screening through to the follow up visit, up to 65 days

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

25 Years to 55 Years
Ages
All
Sex
Accepted
Healthy volunteers
Inclusion Criteria: * Medically healthy based on medical records and study specific assessments Exclusion Criteria: * Presence or history of severe adverse reaction to any drug or drug excipient

Where

1 study site

FacilityCityRegionCountry
Hammersmith Medicines ResearchLondonUnited Kingdom

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT05347849 on ClinicalTrials.gov →

Last updated in the registry 2024-03-18. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits