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OpenTrials
Completed

NCT Number: NCT04083261

Pharmacogenetic Variation: Factors That May Affect the Efficacy and Safety of Medical Marijuana

The primary purpose of this research is to identify genetic factors that may affect the efficacy and safety of medical marijuana, regardless of condition. The pharmacogenomics test detects DNA variants, which may affect the way drugs work and are metabolized in the body and/or detect potential side effects.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Columbia Care New York Dispensary

New York, 10003, United States

About this study

This observational, population-based study will examine genetic differences between ultra-rapid, intermediate and poor metabolizers of various formulations of Columbia Care's medical cannabis products in order to identify genetic factors that may affect the efficacy and safety of medical marijuana, regardless of condition. The goal of the research is to establish relationships between cannabis consumers, cannabinoids, and consumer outcomes. The study is expected to enroll 150 subjects across three cohorts, high daily dose users (poor metabolizers) that take more than 50 mg of cannabinoids daily (n=50), low daily dose users (ultra-rapid metabolizers) that take less than 10 mg of cannabinoids daily (n=50), and a control group (intermediate metabolizers) that represents the median daily dose user taking between 11-21 mg of cannabinoids daily (n=50).

Columbia Care Inc. has identified trends amongst its medical cannabis users suggesting that there are some patients who are "high daily dose users" and others who are "low daily dose users", with both groups assumed to have similar satisfaction with the products. The complexity of the endocannabinoid system combined with individual genetic predisposition and gene-environment interactions likely result in the variation in response seen with cannabinoid treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and Females age 18 and older
  • Currently obtaining medical marijuana products from Columbia Care LLC
  • Willing to participate and consent to a DNA analysis
  • Purchased product from Columbia Care for three consecutive encounters spanning a 6-month period

Exclusion criteria

  • Unwillingness to participate and consent to a DNA analysis
  • Unwillingness to answer a survey/questionnaire on patient satisfaction as related to product efficacy

Treatment and study plan

DNA Genotek Oragene 600

Other

Saliva-based DNA sample collection kit

Primary outcomes

  1. Identification of genetic factors

    Time frame: Day 1

    Saliva-based DNA sample will be tested for known genes (e.g., the cytochrome P-450 superfamily)

Secondary outcomes

  1. Satisfaction with therapy and adverse effects: survey

    Time frame: Day 1

    Survey tool will examine patient satisfaction with current dose as a covariate and evaluate adverse outcomes (e.g., mental health indications, reported unintended effects) based on varying doses and mode of exposure of cannabis within our analyses.

Sponsors and collaborators

Lead sponsor

Columbia Care Inc.

Other

Registry information

Official study title

An Observational, Population-Based Study of Pharmacogenetic Variation to Identify Genetic Factors That May Affect the Efficacy and Safety of Medical Marijuana

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Sep 10, 2019
Registry last updated
Jul 10, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.