Tozadenant
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|---|---|
| Other names | RO4494351; RO-4494351; SYN-115; SYN115 |
| Routes of administration | Oral[1] |
| Drug class | Adenosine A2A receptor antagonist; Antiparkinsonian agent |
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| Pharmacokinetic data | |
| Elimination half-life | 15 hours[2] |
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| PDB ligand | |
| Chemical and physical data | |
| Formula | C19H26N4O4S |
| Molar mass | 406.50 g·mol−1 |
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Tozadenant (INN, USAN; developmental code names RO4494351 and SYN-115) is an adenosine A2A receptor antagonist which was under development for the treatment of Parkinson's disease and liver disorders but was never marketed due to safety concerns.[1][3] It is taken orally.[1] Tozadenant was under development by Roche, Acorda Therapeutics, and Biotie Therapies.[1] It reached phase 3 clinical trials for Parkinson's disease prior to the discontinuation of its development.[1] The development of tozadenant was discontinued due to findings of agranulocytosis and associated serious adverse effects in clinical trials including five patient deaths.[1][4][5]
See also
References
- ^ a b c d e f "Acorda Therapeutics". AdisInsight. 5 November 2023. Retrieved 28 January 2026.
- ^ Mancel V, Mathy FX, Boulanger P, English S, Croft M, Kenney C, et al. (August 2017). "Pharmacokinetics and metabolism of [14C]-tozadenant (SYN-115), a novel A2a receptor antagonist ligand, in healthy volunteers". Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 47 (8): 705–718. doi:10.1080/00498254.2016.1221164. PMID 27489076.
- ^ Perez-Lloret S, Merello M (June 2014). "Two new adenosine receptor antagonists for the treatment of Parkinson's disease: istradefylline versus tozadenant". Expert Opinion on Pharmacotherapy. 15 (8): 1097–1107. doi:10.1517/14656566.2014.903924. PMID 24673462.
- ^ Taylor P (15 November 2017). "Acorda slumps on safety fears for Parkinson's drug tozadenant". Fierce Biotech. Retrieved 28 January 2026.
- ^ Taylor NP (20 November 2017). "Acorda dumps $363M Parkinson's drug after patient deaths". Fierce Biotech. Retrieved 28 January 2026.