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Clinical Trial Summary

Basic characterization of the drug delivery system for cannabidiol. A comparative bioavailability study.


Clinical Trial Description

This study aims to investigate an innovative pharmaceutical preparation of cannabidiol. Thus, a comparative bioavailability study will be conducted, comparing cannabidiol capsules (reference formulation) with an intranasal cannabidiol gel (test formulation), with the further aim to find an appropriate dosing of the new pharmaceutical preparation. The intranasal administration may also be suitable to reduce the high variability in the bioavailability of cannabidiol observed for the current oral administration. ;


Study Design


Related Conditions & MeSH terms

  • Pharmacokinetics, Bioavailability

NCT number NCT03471559
Study type Interventional
Source Central Institute of Mental Health, Mannheim
Contact
Status Terminated
Phase Phase 1
Start date December 10, 2018
Completion date August 29, 2019