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The future of endocannabinoid-oriented clinical research after CB1 antagonists

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Abstract

Introduction

Great interest has been shown by the medical community and the public in the cannabinoid CB1 receptor antagonists, such as rimonabant, for treatment of obesity, metabolic syndrome, and possibly drug addiction.

Discussion

This novel class of drug has therapeutic potential for other disorders, as the endocannabinoid system is involved in various health conditions. However, rimonabant, the first clinically available member of this class of drugs, has been linked to increased risk of anxiety, depression, and suicidality. Due to those risks, the European Medicines Agency called for its withdrawal from the market in October, 2008. Shortly after this decision, several pharmaceutical companies (Sanofi-aventis, Merck, Pfizer, Solvay) announced that they would stop further clinical research on this class of drug. Here, we provide an overview of those events and make several suggestions for continuing such clinical research, while safeguarding the safety of patients and clinical trial subjects.

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Acknowledgment

Drs. Gorelick and Goldberg are supported by the Intramural Research Program, NIH, National Institute on Drug Abuse. Dr. Gorelick was an investigator in clinical trials of rimonabant at NIDA sponsored by Sanofi. He did not personally receive any funding from Sanofi. Drs. Le Foll and Goldberg report no competing interests.

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Correspondence to Bernard Le Foll.

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Le Foll, B., Gorelick, D.A. & Goldberg, S.R. The future of endocannabinoid-oriented clinical research after CB1 antagonists. Psychopharmacology 205, 171–174 (2009). https://doi.org/10.1007/s00213-009-1506-7

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  • DOI: https://doi.org/10.1007/s00213-009-1506-7

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