Post Marketing Surveillance(PMS) Study of Lorviqua in Korea
NCT05599412 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 600
Last updated 2026-03-27
Summary
The objective of this study is to monitor the usage of Lorviqua in real practice within label, including the adverse events associated with Lorviqua
Conditions
- Metastatic ALK+ Non Small Cell Lung Cancer
Interventions
- DRUG
-
Lorviqua
As provided in real world practice
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-05-22
- Primary Completion
- 2028-01-31
- Completion
- 2028-01-31
Countries
- South Korea
Study Locations
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