CompletedPhase 1

Single Ascending Dose Study With BPL-003 in Healthy Subjects

United Kingdom62 participantsStarted 2022-02-14

Plain-language summary

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

Who can participate

Age range25 Years – 55 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Percentage of subjects with treatment emergent AEs (TEAES)

Timeframe: From screening through to the follow up visit, up to 65 days

Trial details

NCT IDNCT05347849

SponsorBeckley Psytech Limited

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2024-01-19

View on ClinicalTrials.gov More Pharmacokinetics in Healthy Adults trials