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

PHASE1RecruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

October 26, 2024

Primary Completion Date

November 30, 2025

Study Completion Date

November 30, 2025

Conditions
Pharmacokinetics
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.

Trial Locations (1)

S7N 5E5

RECRUITING

University of Saskatchewan, Saskatoon

All Listed Sponsors
collaborator

University of Regina

OTHER

lead

University of Saskatchewan

OTHER