Insys Therapeutics announced that the United States Food and Drug Administration had granted orphan drug designation to its proprietary cannabidiol product for the treatment of glioma. (A glioma is a type of tumor that starts in the brain or spine.)

To be granted orphan drug designation, the pharmaceutical must generally be intended to treat a disease that affects less than 200,000 people, although there are exceptions. Companies can apply for ODD through an FDA application. Part of this application includes a discussion of the scientific rationale for why the drug could benefit the intended disease. Acceptable evidence includes in vitro studies, preclinical animal testing, and any relevant human experience. If the rationale is not strong enough, then the FDA would reasonably deny the application.

Orphan Drug Designation for CBD

The fact that the FDA has granted ODD to a CBD product for treating glioma is remarkably important. It means the United States government believes the scientific evidence is strong enough to justify directly treating brain cancer in humans with a cannabinoid. They would have simply denied the application if there were no tangible merits, but such approval expressly implies real therapeutic potential.

This progress is impressively significant, but there is still much to be desired.

First, cannabinoids work best when used together, so a CBD-only treatment will probably yield poorer results than a formula with CBD, THC, and the dozens of other cannabinoids. It is also likely that the CBD being used by Insys is synthetic. While organic whole-plant, full-spectrum cannabis extracts are best, the FDA approval for CBD alone is still a major step.

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