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A Study to Evaluate Treatment Preferences for Japanese Participants With Muscle-invasive Urothelial Carcinoma of the Bladder (SNUGGLE)

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status

Completed

Conditions

Urinary Bladder Neoplasms

Study type

Observational

Funder types

Industry

Identifiers

NCT05742867
CA209-6M4

Details and patient eligibility

About

The main purpose of this study is to identify important treatment attributes for post-radical cystectomy (RC) treatment for participants with MIBC (Muscle-Invasive Bladder Cancer) and assess the relative importance of treatment attributes for post-RC treatment in Japan.

Enrollment

115 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Must reside in Japan and able to speak/read Japanese for the interview/survey

  • Must have a clinical diagnosis of Muscle-invasive bladder cancer (MIBC):

    • ypT2-ypT4a or ypN+ MIBC, with prior neoadjuvant cisplatin chemotherapy and underwent radical cystectomy
    • pT3-pT4a or pN+ MIBC, without prior neoadjuvant cisplatin chemotherapy and underwent radical cystectomy
  • Must not have received any treatment related to MIBC after radical cystectomy

Exclusion criteria

  • Determined by the physician as being unsuitable for the study (e.g. having any clinically significant psychiatric disorder, cognitive impairment, or having difficulty with communicating in Japanese)
  • Confirmed diagnosis of other primary cancers at the time of obtaining consent
  • Current participation in a MIBC clinical trial

Trial design

115 participants in 1 patient group

Cohort 1
Description:
High-risk Muscle-Invasive Bladder Cancer (MIBC) participants following radical cystectomy

Trial contacts and locations

1

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Central trial contact

First line of the email MUST contain NCT # and Site #.; BMS Study Connect Contact Center http://www.bmsstudyconnect.com

Data sourced from clinicaltrials.gov

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