Evidence map›Paper›PMID 32918835›Full record

ReviewEpilepsia2020

Clinical implications of trials investigating drug-drug interactions between cannabidiol and enzyme inducers or inhibitors or common antiseizure drugs.

Philip N Patsalos, Jerzy P Szaflarski, Barry Gidal, Kevan VanLandingham, David Critchley, Gilmour Morrison

Open access · hybridAbstract readReview
In one paragraph

Review in Epilepsia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. (+)-Trans-Cannabidiol Is an Agonist at Human CBPharmacology research & perspectives · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Utilization of Cannabidiol in Post-Organ-Transplant Care.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Impact of Age and Concurrent Antiseizure Medication Use on Lacosamide Dose to Concentration Ratio and Dosing in Pediatric Patients.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Philip N PatsalosDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.ORCID 0000-0003-2439-7404
Jerzy P SzaflarskiDepartment of Neurology and University of Alabama at Birmingham Epilepsy Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0000-0002-5936-6627
Barry GidalSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Kevan VanLandinghamGreenwich Biosciences, Inc., Carlsbad, California, USA.
David CritchleyGW Research Ltd, Cambridge, UK.
Gilmour MorrisonGW Research Ltd, Cambridge, UK.ORCID 0000-0002-5320-7721
GW Pharmaceuticals (United Kingdom) · GBNational Hospital for Neurology and Neurosurgery · GBUniversity of Alabama at Birmingham · USUniversity of Wisconsin–Madison · US

Funding

GW Research Ltd, Cambridge, UK
6 · The paper itself

Abstract

Highly purified cannabidiol (CBD) has demonstrated efficacy with an acceptable safety profile in patients with Lennox-Gastaut syndrome or Dravet syndrome in randomized, double-blind, add-on, controlled phase 3 trials. It is important to consider the possibility of drug-drug interactions (DDIs). Here, we review six trials of CBD (Epidiolex/Epidyolex; 100 mg/mL oral solution) in healthy volunteers or patients with epilepsy, which investigated potential interactions between CBD and enzymes involved in drug metabolism of common antiseizure drugs (ASDs). CBD did not affect CYP3A4 activity. Induction of CYP3A4 and CYP2C19 led to small reductions in exposure to CBD and its major metabolites. Inhibition of CYP3A4 activity did not affect CBD exposure and caused small increases in exposure to CBD metabolites. Inhibition of CYP2C19 activity led to a small increase in exposure to CBD and small decreases in exposure to CBD metabolites. One potentially clinically important DDI was identified: combination of CBD and clobazam (CLB) did not affect CBD or CLB exposure, but increased exposure to major metabolites of both compounds. Reduction of CLB dose may be considered if adverse reactions known to occur with CLB are experienced when it is coadministered with CBD. There was a small increase of exposure to stiripentol (STP) when coadministered with CBD. STP had no effect on CBD exposure but led to minor decreases in exposure to CBD metabolites. Combination of CBD and valproate (VPA) did not cause clinically important changes in the pharmacokinetics of either drug, or 2-propyl-4-pentenoic acid. Concomitant VPA caused small increases in exposure to CBD metabolites. Dose adjustments are not likely to be necessary when CBD is combined with STP or VPA. The safety results from these trials were consistent with the known safety profile of CBD. These trials indicate an overall low potential for DDIs between CBD and other ASDs, except for CLB.

Indexed as

AnticonvulsantsCannabidiolClinical Trials as TopicClobazamCytochrome P-450 CYP2C19Cytochrome P-450 CYP2C19 InducersCytochrome P-450 CYP2C19 InhibitorsCytochrome P-450 CYP3ACytochrome P-450 CYP3A InducersCytochrome P-450 CYP3A InhibitorsDioxolanesDose-Response Relationship, DrugDrug InteractionsDrug Therapy, CombinationEpilepsies, MyoclonicFatty Acids, Monounsaturated2-propyl-4-pentenoic acidAnticonvulsantsCannabidiolClobazamCytochrome P-450 CYP2C19Cytochrome P-450 CYP2C19 InducersCytochrome P-450 CYP2C19 InhibitorsCytochrome P-450 CYP3ACytochrome P-450 CYP3A InducersCytochrome P-450 CYP3A InhibitorsDioxolanesFatty Acids, MonounsaturatedstiripentolValproic AcidclobazamDravet syndromeLennox-Gastaut syndromestiripentolvalproate

Identifiers

PMID32918835
PMCPMC7693203
OpenAlexW3086907524

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.