The role of cytochrome P450 polymorphisms in the pharmacokinetics of oral esketamine.
Daniël T Coerts, Sanne Y Smith-Apeldoorn, Jérôme C Oude Nijhuis, Ron H N Van Schaik, Wim J Tamminga, Daan J Touw, Jolien K E Veraart, Robert A Schoevers, Jens H van Dalfsen
The pharmacogenomics journal April 24, 2026 DOI: 10.1038/s41397-026-00405-5 via PubMed
Summary
A genetic variation in the CYP2B6 enzyme, known as 516 G > T, is linked to higher blood levels of oral esketamine four hours after dosing in people with treatment-resistant depression. In a small sample of 18 participants from a placebo-controlled trial, carriers of the variant had median esketamine levels of 5.1 µg/L, compared to 2.1 µg/L in non-carriers. No significant associations were found for two other genetic variants, CYP3A4*22 and CYP3A5*3, but the numbers of carriers were very small. Larger studies are needed to clarify their effects.
Study at a glance
| Characteristics | Placebo-controlled trial Peer reviewed |
|---|---|
| Sample size | 18 |
| Population | Patients with treatment-resistant depression |
| Key finding | CYP2B6 516 G > T carriers had higher esketamine plasma levels than non-carriers. |
Abstract
Oral esketamine displays therapeutic potential for treatment-resistant depression. However, treatment is complicated by a low and variable bioavailability. Genetic polymorphisms in the cytochrome P450 (CYP) enzymes responsible for esketamine's metabolism may influence bioavailability. In a subsample of patients included in a placebo-controlled trial investigating repeated, low dose oral esketamine (N = 18), blood samples were collected four hours after dosing. CYP2B6 516 G > T, CYP3A4*22, and CYP3A5*3 genotyping was performed, and the plasma levels of esketamine and its metabolites were measured. CYP2B6 516 G > T carriers (Mdn = 5.1 µg/L) demonstrated higher esketamine plasma levels compared to non-carriers (Mdn = 2.1 µg/L) (U = 45.00, p = 0.032). No significant associations were observed for CYP3A4*22 carriership (n = 2) or CYP3A5*3 heterozygosity (n = 2), nor for esketamine's metabolites. In summary, CYP2B6 516 G > T is associated with higher esketamine plasma concentrations. Further research with more participants is warranted to draw conclusions about CYP3A4*22 and CYP3A5*3. Clinical trial registration: NTR6161 (Dutch Trial Register).