Minzasolmin
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| IUPAC name
N-[(2R)-1-(1H-indol-3-yl)hexan-2-yl]-2-(4-methylpiperazin-1-yl)-1,3-thiazole-5-carboxamide | |
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| Properties | |
| C23H31N5OS | |
| Molar mass | 425.60 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Minzasolmin (development names DLX313 and UCB0599) is an experimental small-molecule drug in development for Parkinson's disease that is designed to prevent misfolding of α-synuclein.[1][2] On December 16, 2024 UCB reported the results of a phase II clinical trial on minzasolmin for Parkinson's involving 496 people, stating that the drug failed to demonstrate superiority over placebo in both primary and secondary endpoints.[3]
See also
References
- ↑ Schwarz, Thomas C.; Beier, Andreas; Ledolter, Karin; Gossenreiter, Thomas; Höfurthner, Theresa; Hartl, Markus; Baker, Terry S.; Taylor, Richard J.; Konrat, Robert (11 April 2023). "High-resolution structural information of membrane-bound α-synuclein provides insight into the MoA of the anti-Parkinson drug UCB0599". Proceedings of the National Academy of Sciences. 120 (15) e2201910120. Bibcode:2023PNAS..12001910S. doi:10.1073/pnas.2201910120. PMC 10104497. PMID 37027427. S2CID 258007748.
- ↑ Price, Diana L.; Khan, Asma; Angers, Rachel; Cardenas, Alvaro; Prato, Maria Key; Bani, Massimo; Bonhaus, Douglas W.; Citron, Martin; Biere, Anja-Leona (17 July 2023). "In vivo effects of the alpha-synuclein misfolding inhibitor minzasolmin supports clinical development in Parkinson's disease". npj Parkinson's Disease. 9 (1): 114. doi:10.1038/s41531-023-00552-7. ISSN 2373-8057. PMC 10352257. PMID 37460603.
- ↑ Masson, Gabrielle (16 December 2024). "UCB-Novartis Parkinson's asset fails to improve symptoms". www.fiercebiotech.com. Retrieved 7 July 2026.
