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Safety and efficacy for day 1 administration of gemcitabine and cisplatin

Safety and efficacy for day 1 administration of gemcitabine and cisplatin - Safety and efficacy for day 1 administration of gemcitabine and cisplatin

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031015
Enrollment
20
Registered
2018-01-27
Start date
2018-01-25
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

Urothelial carcinoma

Interventions

gemcitabine and cisplatin

Sponsors

Tokyo Metropolitan Tama Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: urothelial carcinoma

Exclusion criteria

Exclusion criteria: nothing

Design outcomes

Primary

MeasureTime frame
Safety

Countries

Japan

Contacts

Public ContactTakeshi Azuma

Tokyo Metropolitan Tama Medical Center Urology

tazuma-tky@umin.ac.jp042-323-5111

Outcome results

None listed

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