Korea Post Marketing Surveillance (PMS) Study of Vizimpro

Status Enrolling by invitation

Clinical Trial Summary

Vizimpro will be approved for the treatment of EGFR NSLCL 1L in Korea. In accordance with the Standards for Re-examination of New Drug, it is required to conduct a PMS. Post marketing surveillance is required to determine any problems or questions associated with Vizimpro after marketing in Korea, with regard to the following clauses under conditions of general clinical practice. Therefore, through this study, effectiveness and safety of Vizimpro will be observed.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Lung Neoplasms

Clinical Trial Details

NCT number	NCT04721106
Study type	Observational
Source	Pfizer
Contact
Status	Enrolling by invitation
Phase
Start date	March 12, 2021
Completion date	March 30, 2026

View Details

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