News Release

French drug trial details murky, should not influence future cannabinoid research

Peer-Reviewed Publication

Mary Ann Liebert, Inc./Genetic Engineering News

<em>Cannabis and Cannabinoid Research</em>

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Cannabis and Cannabinoid Research is the only peer-reviewed open access journal dedicated to the scientific, medical, and psychosocial exploration of clinical cannabis, cannabinoids, and the endocannabinoid system. The Journal publishes a broad range of human and animal studies including basic and translational research; clinical studies; behavioral, social, and epidemiological issues; and ethical, legal, and regulatory controversies.

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Credit: ©Mary Ann Liebert, Inc., publishers

New Rochelle, NY, January 19, 2016--Contrary to initial reports, the drug tested on paid volunteers in a French study, which resulted in one death and five hospitalizations, did not contain cannabis or cannabinoids. The drug, an FAAH inhibitor manufactured by the Portuguese company Bial, was instead designed to act upon the human endocannabinoid system as a potential painkiller and treatment for anxiety. Beyond that, very little information is publicly known and as such, no conclusions can be drawn about the safety or efficacy related to future cannabis and cannabinoid research.

"Without adequate information it is impossible to advance any realistic theory about causes of toxicity," says Daniele Piomelli, PhD, Louise Turner Arnold Chair in Neurosciences and Professor, Anatomy & Neurobiology University of California-Irvine, School of Medicine, and Editor-in-Chief of Cannabis and Cannabinoid Research. "Several structurally different FAAH inhibitors have been previously tested for human safety in rigorous Phase 1 clinical trials. These include compounds from Sanofi, Pfizer, Merck, Johnson and Johnson, and others. All these FAAH inhibitors were shown to be safe in humans."

The human safety of multiple FAAH inhibitors suggests that toxicity of the Bial compound is unlikely to be a 'class effect'--in other words, it is unlikely to be due to the interaction of the Bial compound with FAAH.

"It is more probable that the Bial compound interacts with another, as yet unknown protein that is responsible for the observed toxicity, or that a toxic impurity was present in the test drug," continues Dr. Piomelli. "Of course, while we can tentatively exclude a class effect at this point, we cannot pin-point which other target might be responsible for the toxicity of the Bial compound."

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Cannabis and Cannabinoid Research is the only peer-reviewed open access journal dedicated to the scientific, medical, and psychosocial exploration of clinical cannabis, cannabinoids, and the endocannabinoid system. The Journal publishes a broad range of human and animal studies including basic and translational research; clinical studies; behavioral, social, and epidemiological issues; and ethical, legal, and regulatory controversies.

About the Publisher

Mary Ann Liebert, Inc., publishers is a privately held, fully integrated media company known for establishing authoritative peer-reviewed journals in many promising areas of science and biomedical research, including Journal of Medicinal Food, The Journal of Alternative and Complementary Medicine, and Journal of Child and Adolescent Psychopharmacology. A complete list of the firm's 80 journals, books, and newsmagazines is available on the Mary Ann Liebert, Inc., publishers website.


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