Cost-effectiveness analysis of xanomeline and trospium chloride for the treatment of adults with schizophrenia in the US

AIM: The objective of this analysis was to evaluate the cost-effectiveness of xanomeline and trospium chloride (KarXT) as first line (1 L) treatment for adults with schizophrenia from a third-party US payer perspective compared with commonly used antipsychotics, considering both costs and patient quality of life. METHODS: A decision tree-Markov hybrid approach was used to develop an economic model which included both acute and maintenance phases, accounting for probability of treatment response, discontinuation, relapse, adverse events, and death over a lifetime horizon. Clinical data were drawn from published trials, with costs and utilities coming from publicly available sources. Incremental cost-effectiveness ratios (ICERs) were calculated, and sensitivity and scenario analyses were performed to test the robustness of the results. RESULTS: In the base case analysis, KarXT was found to be more costly but more effective than common generic antipsychotics, yielding cost-effective ICERs, and less costly and more effective than branded antipsychotics. The model was associated with moderate sensitivity to treatment response inputs. Scenario analyses showed that implementation of a societal perspective, no tardive dyskinesia risk for KarXT, and a 50% reduction KarXT's relapse probability improved the cost-effectiveness of KarXT. Conversely, a 50% increase in KarXT's relapse probability and a second line analysis worsened cost-effectiveness. LIMITATIONS: At the time of the analysis, relapse data did not exist for KarXT therefore an average of other treatments was assumed and tested in a sensitivity analysis. Also, patients may receive multiple lines of therapy in a lifetime, however, the model only incorporated three lines of treatment. CONCLUSIONS: KarXT, the first schizophrenia medication in 70 years with a non-dopaminergic mechanism of action, is a valuable and potentially cost-effective 1 L treatment option, highlighting the need for continued innovation in this disease space.

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Publication Details

Journal
Journal of Medical Economics
Published
2026-05-09
DOI
https://doi.org/10.1080/13696998.2026.2664332
Primary Topic
Schizophrenia research and treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Cost-effectiveness analysis of xanomeline and trospium chloride for the treatment of adults with schizophrenia in the US

Matthew Sidovar, Ken Kramer, Tyler Mantaian, Andrew J. Cutler et al.
Journal of Medical Economics
Schizophrenia research and treatment
article

Cost-effectiveness analysis of xanomeline and trospium chloride for the treatment of adults with schizophrenia in the US

Matthew Sidovar, Ken Kramer, Tyler Mantaian, Andrew J. Cutler, Kristin Gillard, Jonathan Kowalski
article en

Abstract

AIM: The objective of this analysis was to evaluate the cost-effectiveness of xanomeline and trospium chloride (KarXT) as first line (1 L) treatment for adults with schizophrenia from a third-party US payer perspective compared with commonly used antipsychotics, considering both costs and patient quality of life. METHODS: A decision tree-Markov hybrid approach was used to develop an economic model which included both acute and maintenance phases, accounting for probability of treatment response, discontinuation, relapse, adverse events, and death over a lifetime horizon. Clinical data were drawn from published trials, with costs and utilities coming from publicly available sources. Incremental cost-effectiveness ratios (ICERs) were calculated, and sensitivity and scenario analyses were performed to test the robustness of the results. RESULTS: In the base case analysis, KarXT was found to be more costly but more effective than common generic antipsychotics, yielding cost-effective ICERs, and less costly and more effective than branded antipsychotics. The model was associated with moderate sensitivity to treatment response inputs. Scenario analyses showed that implementation of a societal perspective, no tardive dyskinesia risk for KarXT, and a 50% reduction KarXT's relapse probability improved the cost-effectiveness of KarXT. Conversely, a 50% increase in KarXT's relapse probability and a second line analysis worsened cost-effectiveness. LIMITATIONS: At the time of the analysis, relapse data did not exist for KarXT therefore an average of other treatments was assumed and tested in a sensitivity analysis. Also, patients may receive multiple lines of therapy in a lifetime, however, the model only incorporated three lines of treatment. CONCLUSIONS: KarXT, the first schizophrenia medication in 70 years with a non-dopaminergic mechanism of action, is a valuable and potentially cost-effective 1 L treatment option, highlighting the need for continued innovation in this disease space.

Journal of Medical EconomicsVol. 29(1)
Luminex (United States) (US), Bristol-Myers Squibb (Germany) (DE), SUNY Upstate Medical University (US), Bristol-Myers Squibb (Sweden) (SE), Bristol-Myers Squibb (Belgium) (BE)
Openalex Percentile: Top 5%
Schizophrenia research and treatment
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