Tebideutorexant
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Other names | JNJ-61393215; JNJ-3215 |
Routes of administration | Oral |
Drug class | Orexin receptor antagonist |
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Elimination half-life | 14–25 hours[1] |
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Formula | C23H16D2F4N4O2 |
Molar mass | 460.428 g·mol−1 |
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Tebideutorexant[2] (developmental code names JNJ-61393215, JNJ-3215) is an orexin antagonist medication which is under development for the treatment of depression and anxiety disorders.[3][4][5][6] The drug was originated and developed by Janssen Pharmaceuticals.[3]
It is an orally active compound and acts as a selective antagonist of the orexin OX1 receptor (1-SORA).[4][5][6] Preliminary clinical findings suggest that tebideutorexant may have anti-panic effects in humans.[4][5] The elimination half-life of tebideutorexant is 13.6 to 24.6 hours.[1]
As of June 2023, tebideutorexant is in phase 2 clinical trials for the treatment of major depressive disorder while no further development has been reported for treatment of panic disorder and other anxiety disorders.[3] In 2025, a phase 2a, double-blind, placebo-controlled trial in adults with major depressive disorder and anxious distress found that adjunctive tebideutorexant did not significantly improve depressive symptoms on the Hamilton Rating Scale for Depression or anxiety on the Hamilton Anxiety Rating Scale compared with placebo.[7]
See also
[edit]- List of investigational antidepressants § Orexin receptor antagonists
- List of investigational anxiolytics
References
[edit]- ^ a b Brooks S, Zuiker R, Bleys C, Ziagkos D, Moyer J, van Nueten L, et al. (2023). "Pharmacological characterization of the selective orexin-1 receptor antagonist JNJ-61393215 in healthy volunteers". Journal of Psychopharmacology. 37 (6): 577–589. doi:10.1177/02698811231167989. hdl:1887/3720682. ISSN 0269-8811. PMID 37165642. Retrieved 27 July 2025.
- ^ PubChem. "Tebideutorexant". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-08-15.
- ^ a b c "JNJ 61393215 - AdisInsight".
- ^ a b c Caldirola D, Alciati A, Cuniberti F, Perna G (2021). "Experimental Drugs for Panic Disorder: An Updated Systematic Review". Journal of Experimental Pharmacology. 13: 441–459. doi:10.2147/JEP.S261403. PMC 8055642. PMID 33889031.
- ^ a b c Jacobson LH, Hoyer D, de Lecea L (May 2022). "Hypocretins (orexins): The ultimate translational neuropeptides". Journal of Internal Medicine. 291 (5): 533–556. doi:10.1111/joim.13406. PMID 35043499. S2CID 248119793.
- ^ a b Salvadore G, Bonaventure P, Shekhar A, Johnson PL, Lord B, Shireman BT, et al. (September 2020). "Translational evaluation of novel selective orexin-1 receptor antagonist JNJ-61393215 in an experimental model for panic in rodents and humans". Translational Psychiatry. 10 (1): 308. doi:10.1038/s41398-020-00937-9. PMC 7477545. PMID 32895369.
- ^ Schmidt ME, Moyer JA, Kezic I, Zhou X, Samtani MN, Bleys C, et al. (June 2025). "Efficacy, safety, and tolerability of JNJ-61393215 (tebideutorexant), a selective orexin-1 receptor antagonist, as adjunctive treatment for major depressive disorder with anxious distress: A double-blind, placebo-controlled, randomized phase 2a study". European Neuropsychopharmacology. 95: 14–23. doi:10.1016/j.euroneuro.2025.03.007. PMID 40215570.