CYB003
| Clinical data | |
|---|---|
| Other names | CYB-003; deuterated psilocybin analogue; deuterated psilocin analogue |
| Routes of administration | By mouth |
| Drug class | Serotonergic psychedelic |
| ATC code |
|
| Pharmacokinetic data | |
| Onset of action | 30 minutes (Cmax) (rats) |
| Elimination half-life | 45 minutes (rats) |
CYB003, or CYB-003, also known as deuterated psilocybin analogue, is a serotonergic psychedelic related to psilocybin which is under development for the treatment of major depressive disorder, alcoholism, and other psychiatric disorders. It is taken by mouth.
It is a tryptamine derivative and is a deuterated analogue of psilocybin and psilocin. The pharmacodynamic profile of CYB003, including its interactions with serotonin receptors and its effects in animals, is similar to that of psilocin. As with psilocin, CYB003 is a potent agonist of the serotonin 5-HT2A receptor and produces psychedelic-like effects in animals. However, it was developed to have improved pharmacokinetic properties compared to psilocybin, including reduced variability in circulating levels, a faster onset of action, and a shorter duration.
As of October 2024, CYB003 is in phase 3 clinical trials for major depressive disorder and is in the preclinical stage of development for alcoholism and other psychiatric disorders. Two phase 3 clinical trials for major depressive disorder are being initiated in November 2024 and February 2025. The drug is under development by Cybin. The chemical structure of CYB003 has not yet been disclosed. However, Cybin patented deuterated tryptamines including the dideuterated psilocin analogue PI-α,α-d2 (psilocin dideuterated at the α carbon) in 2023. Other related drugs include the deuterated tryptamine CYB004, the deuterated phenethylamine CYB005, and the phenethylamine CYB210010.
An INN of deupsilocin for a deuterated form of psilocin called d10-psilocin with CAS number 1435934-64-7 was proposed in 2023 and recommended in 2024. This deuterated analogue of psilocin was patented in 2021 by Lennham Pharmaceuticals. It is said to be in phase 3 trials.