Imfinzi/Imjudo NSCLC Japan PMS_Japan Post-Marketing Surveillance (PMS) Study - CEI/SCEI
NCT05826366 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 296
Last updated 2026-04-14
Summary
To collect information of safety in patients with unresectable advanced or recurrent non-small cell lung cancer who receive combination therapy of IMJUDO, IMFINZI and other platinum-based anti-cancer agents under actual use in the postmarketing setting.
Conditions
- Carcinoma, Non-Small-Cell Lung
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Toshimitsu Tokimoto · AstraZeneca KK
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-06-02
- Primary Completion
- 2025-04-30
- Completion
- 2025-04-30
Countries
- Japan
Study Locations
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