Evidence map›Paper›PMID 41868713›Full record

ArticleSchizophrenia bulletin open2026

A Qualitative Investigation of the Experience of Taking Xanomeline and Trospium Chloride for Schizophrenia, Part 1: Perceived Impact on Symptoms.

William P Horan, Cory Saucier, Peter J Weiden, Amy Claxton, Stephen R Marder, April M Foster, Colin Sauder, Kaitlin LaGasse, Sloan Rucker, Kristi Jackson and 3 more

Abstract read
In one paragraph

Article in Schizophrenia bulletin open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

William P HoranBristol Myers Squibb, Princeton, NJ 08543, United States.
Cory SaucierIQVIA Quality Metric Inc., Johnston, Rhode Island 02919, United States.
Peter J WeidenDepartment of Psychiatry and Behavioral Health, Renaissance School of Medicine at Stony Brook University, Stony Brook, NY 11794, United States.ORCID https://orcid.org/0000-0001-5583-5871
Amy ClaxtonBristol Myers Squibb, Princeton, NJ 08543, United States.
Stephen R MarderDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, CA 90095, United States.ORCID https://orcid.org/0000-0003-0288-309X
April M FosterIQVIA Quality Metric Inc., Johnston, Rhode Island 02919, United States.
Colin SauderBristol Myers Squibb, Princeton, NJ 08543, United States.
Kaitlin LaGasseIQVIA Quality Metric Inc., Johnston, Rhode Island 02919, United States.
Sloan RuckerIQVIA Quality Metric Inc., Johnston, Rhode Island 02919, United States.
Kristi JacksonIQVIA Quality Metric Inc., Johnston, Rhode Island 02919, United States.
Tej PatelBristol Myers Squibb, Princeton, NJ 08543, United States.
John G SonnenbergUptown Research Institute, Chicago, IL 60640, United States.
Inder KaulBristol Myers Squibb, Princeton, NJ 08543, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Xanomeline and trospium chloride (formerly KarXT) is a muscarinic M Methods: This is a qualitative study embedded within a larger 52-week open-label long-term safety study that investigated patient perspectives on xanomeline/trospium monotherapy in clinically stable outpatients transitioned from previous antipsychotic treatments. A subsample completed up to 2 semi-structured interviews to explore their experience-favorable or unfavorable-approximately 6 weeks ( Results: At study entry, most participants reported symptoms despite ongoing antipsychotic treatment, including positive (auditory hallucinations, >80%), negative (low motivation, >70%), and cognitive (trouble concentrating, >70%) symptoms. Over 60% reported meaningful improvement in one or more symptoms within 6 weeks of starting xanomeline/trospium, increasing to about 80% by 6 months. Less than 10% reported symptom worsening at either time point. Participants described these improvements as personally meaningful, with notable benefits in daily functioning. Discussion: Participants entered this study with various persistent, burdensome schizophrenia symptoms despite ongoing treatment. Most experienced substantial and sustained symptom relief for up to 6 months after initiating xanomeline/trospium treatment. These qualitative findings highlight xanomeline/trospium's potential to provide meaningful relief across multiple symptom domains and support functional recovery. A companion report explores quality of life and medication satisfaction.

Indexed as

qualitative studyschizophreniasubjective experiencexanomeline and trospium

Identifiers

PMID41868713
PMCPMC13000689

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.