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Drs' preference survey for mUC 1L

Drs' preference survey of choosing regimen for mUC 1L in Japan real world practice

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1030250496
Enrollment
200
Registered
2025-11-11
Start date
2025-12-08
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unresectable or metastatic urothelial carcinoma

Interventions

None listed

Sponsors

Minegishi Toshihiko
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Urologists or medical oncologists 2. Physicians who have experience within the past 6 months of administering first-line treatment, excluding best supportive care, to patients with unresectable or recurrent urothelial carcinoma (UC) 3. Physicians who have experience in determining the treatment plan when administering chemotherapy to patients with unresectable or recurrent UC 4. Able to provide informed consent There are other inclusion criteria.

Exclusion criteria

Exclusion criteria: 1. Physicians working in departments other than urology or oncology 2. Physicians working at clinics 3. When the EV-P or gemcitabine-cisplatin plus maintenance avelumab regimen is not registered at the workplace There are other exclusion criteria.

Design outcomes

Primary

MeasureTime frame
The questionnaire will collect data on the demographic characteristics of participating physicians, recent practices regarding first-line treatment for UC patients, and evaluations and expectations concerning available treatment options.

Contacts

Public ContactYuki Suzaki

MSD K.K., Tokyo, Japan

yuki.suzaki@msd.com+81-3-6272-1000

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026