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RECRUITING
NCT06574100
PHASE1

Relative Bioavailability of Two Orally Administered CBD Formulations in Healthy Male Adults

Sponsor: University of Saskatchewan

View on ClinicalTrials.gov

Summary

This project is aimed at understanding whether a new fast-dissolving cheek-administered cannabidiol strip will be absorbed better into the body than cannabidiol powder. The results of this study will help guide dosage formulation choices as well as dosing regimens in NFL athletes for concussion management.

Key Details

Gender

MALE

Age Range

18 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2024-10-26

Completion Date

2025-11

Last Updated

2025-03-30

Healthy Volunteers

Yes

Interventions

DRUG

Cannabidiol

Patients in the first arm cross-over will receive either a single bolus dose of 250mg buccally administered or 1000mg CBD powder and cross over to vice-versa after 21 days.

DRUG

Cannabidiol

Patients will be randomised to receive 3000mg oral CBD fasting or Fed, they will the cross over to the other group 21 days following the first administration.

Locations (1)

University of Saskatchewan

Saskatoon, Saskatchewan, Canada