Imfinzi BTC Japan PMS_Japan Post-Marketing Surveillance (PMS) Study - CEI/SCEI
NCT05835778 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 236
Last updated 2026-01-14
Summary
To investigate onset of adverse drug reactions in patients with curatively unresectable biliary tract cancer who receive IMFINZI in combination with gemcitabine hydrochloride and cisplatin under actual use in the post-marketing setting.
Conditions
- Biliary Tract Cancer
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Toshimitsu Tokimoto · AstraZeneca KK
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-06-06
- Primary Completion
- 2025-11-21
- Completion
- 2025-11-21
Countries
- Japan
Study Locations
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