Evidence map›Paper›PMID 37095473›Full record

ArticleBMC urology2023

Study design of a phase 4, real-world study (COMPOSUR) to evaluate vibegron in patients with overactive bladder.

Roger R Dmochowski, Eric S Rovner, Michael J Kennelly, Diane K Newman, Laleh Abedinzadeh, Daniel Snyder, Elizabeth Thomas, Cornelia Haag-Molkenteller, Matt T Rosenberg

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC urology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05067478 (Composur, a Patient-centric, Phase IV, Open-label, Prospective, Real World US Study to Evaluate Vibegron on Patient Treatment Satisfaction, Quality of Life, and Healthcare Resource Utilization in Overactive Bladder), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
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.

NCT05067478 completednot on this map

Composur, a Patient-centric, Phase IV, Open-label, Prospective, Real World US Study to Evaluate Vibegron on Patient Treatment Satisfaction, Quality of Life, and Healthcare Resource Utilization in Overactive Bladder

TypeobservationalSponsorUrovant Sciences GmbHRan2021 to 2024Enrolled403ConditionsOveractive BladderArmsVibegron
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Observational
  2. Review
  3. Observational
  4. Article
  5. Narrative review of telemedicine applications in decentralized research.Journal of clinical and translational science · 2024
    Review
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

9 authors at 6 institutions in 1 country.

Roger R DmochowskiDepartment of Urologic Surgery, Vanderbilt University Medical Center, 1211 Medical Center Dr, Nashville, TN, 37232, USA. roger.dmochowski@vumc.org.
Eric S RovnerDepartment of Urology, Medical University of South Carolina, Charleston, SC, USA.
Michael J KennellyCarolinas Medical Center, Charlotte, NC, USA.
Diane K NewmanPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Laleh AbedinzadehUrovant Sciences, Irvine, CA, USA.
Daniel SnyderUrovant Sciences, Irvine, CA, USA.
Elizabeth ThomasUrovant Sciences, Irvine, CA, USA.
Cornelia Haag-MolkentellerUrovant Sciences, Irvine, CA, USA.
Matt T RosenbergMid-Michigan Health Centers, Jackson, MI, USA.
Myovant Sciences (United States) · USCarolinas Medical Center · USMedical University of South Carolina · USMercy Health · USUniversity of Pennsylvania · USVanderbilt University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOveractive bladder (OAB) is defined as urinary urgency accompanied by frequency and nocturia, with or without urge urinary incontinence (UUI). Vibegron, a selective β

methodsThis is a 12-month, prospective, observational, real-world study, with an optional 12-month extension to 24 months, in the US assessing adults ≥ 18 years old starting a new course of vibegron. Patients must be previously diagnosed with OAB with or without UUI, symptomatic for ≥ 3 months before enrollment, and receive prior treatment with an anticholinergic, with mirabegron, or with a combination of an anticholinergic and mirabegron. Enrollment is performed by the investigator following exclusion and inclusion criteria guided by US product labeling, reinforcing a real-world approach. Patients complete the OAB Satisfaction with Treatment Questionnaire (OAB-SAT-q) monthly and the OAB Questionnaire short form (OAB-q-SF) and Work Productivity and Activity Impairment Questionnaire (WPAI:US) at baseline and monthly for 12 months. Patients are followed up via phone call, in-person visits, or telehealth (ie, virtual) visits. The primary endpoint is patient treatment satisfaction as determined by the OAB-SAT-q satisfaction domain score. Secondary endpoints include percent positive responses to individual OAB-SAT-q questions, additional OAB-SAT-q domain scores, and safety. Exploratory endpoints include adherence and persistence. DISCUSSION: OAB leads to a significant decrease in quality of life, as well as impairment of work activities and productivity. Persistence with OAB treatments can be challenging, often due to lack of efficacy and adverse effects. COMPOSUR is the first study to provide long-term, prospective, pragmatic treatment data for vibegron in the US and the resultant effect on quality of life among patients with OAB in a real-world clinical setting. Trial registration ClinicalTrials.gov identifier: NCT05067478; registered: October 5, 2021.

Indexed as

Urinary Bladder, OveractiveAcetanilidesAdolescentAdrenergic beta-3 Receptor AgonistsAdultCholinergic AntagonistsHumansMuscarinic AntagonistsObservational Studies as TopicProspective StudiesPyrimidinonesPyrrolidinesQuality of LifeThiazolesTreatment OutcomeAcetanilidesAdrenergic beta-3 Receptor AgonistsCholinergic AntagonistsmirabegronMuscarinic AntagonistsN-(4-((5-(hydroxy(phenyl)methyl)pyrrolidin-2-yl)methyl)phenyl)-4-oxo-4,6,7,8-tetrahydropyrrolo(1,2-a)pyrimidine-6-carboxamidePyrimidinonesPyrrolidinesThiazolesAdherenceAdrenergic beta-3 receptor agonistsAnticholinergicAntimuscarinicMedication persistenceMicturitionTelemedicineUrinary bladderUrinary incontinence

Identifiers

PMID37095473
PMCPMC10124676
OpenAlexW4366996705

What OpenQuestion holds

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Registered trials

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.