| Clinical data | |
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| Other names | IMU-935 |
| Drug class | RORγ agonist/DHODH inhibitor |
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| Chemical and physical data | |
| Formula | C22H18ClF4N5O2 |
| Molar mass | 495.86 g·mol−1 |
| 3D model (JSmol) | |
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Izumerogant (IMU-935) is a drug which acts as both a selective antagonist of the receptor RAR-related orphan receptor gamma (RORγ), and also an inhibitor of the enzyme dihydroorotate dehydrogenase (DHODH). It has antiinflammatory and broad-spectrum antiviral effects, and is also of interest in the treatment of cancer.[1][2][3][4]
References
- Polasek TM, Leelasena I, Betscheider I, Marolt M, Kohlhof H, Vitt D, et al. (May 2023). "Safety, Tolerability, and Pharmacokinetics of IMU-935, a Novel Inverse Agonist of Retinoic Acid Receptor-Related Orphan Nuclear Receptor γt: Results From a Double-Blind, Placebo-Controlled, First-in-Human Phase 1 Study". Clinical Pharmacology in Drug Development. 12 (5): 525–534. doi:10.1002/cpdd.1243. PMID 36938862.
- Herrmann A, Gege C, Wangen C, Wagner S, Kögler M, Cordsmeier A, et al. (November 2024). "Orally bioavailable RORγ/DHODH dual host-targeting small molecules with broad-spectrum antiviral activity". Antiviral Research. 231 106008. doi:10.1016/j.antiviral.2024.106008. PMID 39306285.
- Wu H, Zhong X, Ma N, He Z, Wang G, Lu G, et al. (2 January 2026). "Selective disruption of RORγt-CBFβ interaction by IMU-935 prevents RORγt-dependent Th17 autoimmunity but not thymocyte development". The Journal of Clinical Investigation. 136 (1) e185942. doi:10.1172/JCI185942. PMC 12721887. PMID 41480759.
- Grochot R, Guo C, Carreira S, Crespo M, Welti J, Miranda S, et al. (March 2026). "An Open-label, Phase 1 Dose-finding Study of Single-agent IMU-935, a Novel RORγ/RORγt Inverse Agonist, in Patients with Progressive Metastatic Castration-resistant Prostate Cancer". European Urology Oncology: S2588–9311(26)00051–9. doi:10.1016/j.euo.2026.02.014. PMID 41820163.