CBD-Lipid-PK (CLiP) Study

  • Research type

    Research Study

  • Full title

    Pharmacokinetic study of a novel lipid formulation of cannabidiol compared to a standard formulation

  • IRAS ID

    288415

  • Contact name

    Amy Holton

  • Contact email

    amy.holton@kcl.ac.uk

  • Sponsor organisation

    King's College London

  • Eudract number

    2020-004551-33

  • ISRCTN Number

    ISRCTN18067579

  • Clinicaltrials.gov Identifier

    NCT05032807

  • Duration of Study in the UK

    0 years, 3 months, 1 days

  • Research summary

    Cannabidiol (CBD) has been approved as a treatment for rare childhood epilepsies and could be an effective treatment for psychotic disorders, anxiety disorders and addictions. It is available as an oral liquid and as standard oral capsules.

    The bioavailability of oral cannabidiol is poor (only around 5-10% is absorbed), particularly in the fasted state. With food, its absorption is much higher. In one study, a high-fat breakfast increased the maximum plasma concentration by 4-5 times. As a result of this food effect, when prescribing standard oral formulations of CBD, clinicians should provide advice on dosing the drug according to mealtimes, otherwise, there may be an increased risk of side effects or limited effectiveness.

    One way to reduce the food effect and improve bioavailability is to use lipid encapsulation. In the present study, we will evaluate CBD at the dose that is effective in patients with chronic psychosis (1000mg). The novel formulation will use lipids that are all EU pharmacopoeia approved and have been used in medicinal products before.

    The study aims to assess whether a novel lipid formulation can increase the bioavailability of oral CBD in the fasting state.

  • REC name

    London - Brent Research Ethics Committee

  • REC reference

    22/LO/0047

  • Date of REC Opinion

    1 Feb 2022

  • REC opinion

    Favourable Opinion