Tetrahydrocannabinol/cannabinol/cannabidiol (THC/CBN/CBD), sold under the brand name Zenivol and also known by its developmental code name ZTL-101, is a cannabinoidmedication used for the treatment of insomnia. It is approved and marketed in Germany.
The drug is administered sublingually as a liquid using a syringe about 1 hour before bedtime. Each 0.5 mL dose contains 10 mg δ9-tetrahydrocannabinol (THC), 1 mg cannabinol (CBN), and 0.5 mg cannabidiol (CBD), corresponding to a 20:2:1 mg/mL ratio.
One or two doses are typically taken per night.
The pharmacokinetics of the formulation have been investigated and described in clinical studies.
Pharmacodynamics
THC is a psychoactive cannabinoid acting as a CB1 and CB2 receptorpartial agonist.
CBN is a mildly psychoactive cannabinoid that also acts as a CB1 and CB2 receptor partial agonist.
CBD does not act as an agonist at cannabinoid receptors but modulates the endocannabinoid system and other molecular targets.
THC/CBN/CBD does not significantly alter sleep architecture, aside from a near-significant 3.5% reduction in REM sleep duration.
History
THC/CBN/CBD was approved and launched as a pharmaceutical drug for insomnia in Germany in 2022.
It was developed and is marketed by Zelira Therapeutics.
12345Lavender I, McGregor IS, Suraev A, Grunstein RR, Hoyos CM (August 2022). "Cannabinoids, Insomnia, and Other Sleep Disorders". Chest. 162 (2): 452–465. doi:10.1016/j.chest.2022.04.151. PMID35537535. The most robustly designed study to date examined the safety and efficacy of the cannabinoid formulation ZTL101 (D9-THC 10 mg, CBN 1 mg, and CBD 0.5 mg) relative to placebo in a sample of 23 patients with chronic insomnia disorder.11 Participants self-administered ZTL-101 one hour prior to bedtime for 2 weeks, with the option to double the dose after the fourth night (52% of participants increased the dose). ZTL-101 improved subjective sleep quality by 5.1 points (95% CI, –7.3 to –2.9) on the Insomnia Severity Index and improved self-reported sleep-onset latency, total sleep time, subjective sleep quality, and feelings of rest upon waking. Actigraphy measures indicated reduced wake following sleep onset and increased total sleep time; however, no differences in polysomnography indexes were observed.11 Headaches, xerostomia, dizziness, and "feeling abnormal" were reported more frequently with active treatment (n = 17) than with placebo (n = 4), but these adverse events were self-limiting and did not persist upon wake.