Dextromethorphan/Bupropion: First Approval
- PMID: 36301443
- DOI: 10.1007/s40263-022-00968-4
Dextromethorphan/Bupropion: First Approval
Abstract
An oral, fixed-dose combination of dextromethorphan hydrobromide [an uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist and sigma-1 receptor agonist] and the antidepressant bupropion hydrochloride (an aminoketone and CYP2D6 inhibitor that increases dextromethorphan bioavailability) [AUVELITYTM; dextromethorphan/bupropion], is being developed by Axsome Therapeutics, Inc. for the treatment of major depressive disorder (MDD), Alzheimer's disease agitation and smoking cessation. Dextromethorphan/bupropion was approved in the USA in August 2022 for the treatment of MDD in adults. This article summarizes the milestones in the development of dextromethorphan/bupropion leading to this first approval for the treatment of adults with MDD.
© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
References
-
- World Health Organisation. Depression fact sheet. 2021. https://www.who.int/news-room/fact-sheets/detail/depression . Accessed 13 Sep 2022.
-
- O'Gorman C, Jones A, Kennon K, et al. AXS-05 for neuropsychiatric disorders: scientific rationale and clinical development [abstract no. T16 plus poster]. In: ASCP 2018 Annual Meeting: Treatment of Psychiatric Illness Across the Lifespan. 2018.
-
- Fenton C, Lee A. Glutamatergic modulators are poorly understood, but promising therapies in depressive disorders. Drugs Therapy Perspect. 2022;38(1):7–12. - DOI
Publication types
MeSH terms
Substances
Associated data
LinkOut - more resources
Full Text Sources
