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Spots Global Cancer Trial Database for Lazertinib Real-world Observational Study of in Pre-treated EGFR T790M Mutant With Advanced Non-small Cell Lung Cancer

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Trial Identification

Brief Title: Lazertinib Real-world Observational Study of in Pre-treated EGFR T790M Mutant With Advanced Non-small Cell Lung Cancer

Official Title: Lazertinib Real-world Observational Study of in Pre-treated EGFR T790M Mutant With Advanced Non-small Cell Lung Cancer

Study ID: NCT05377788

Interventions

Lazertinib

Study Description

Brief Summary: * It is to evaluate the safety and effectiveness of a lasertinib(LECLAZA) single drug in a actual medical environment for patients 1. Primary Purpose: Progression-free survival (PFS) 2. Secondary Purpose: * Objective response rate * Time to treatment failure * Adverse event (AE), serious adverse event (SAE), and adverse event of special interest (AESI) * Severity of (S)AE * duration of response (DoR) * Overall survival (OS) * Intravenous Progressive Survival Period (Intracranial PFS) * Relative dose intensity * Research Design : a Multi-Center Prospective and Restrospective Cohort Study

Detailed Description: □ the purpose of the study The study aims to explore the safety, efficacy and resistance of test drugs in patients with local progressive or metastatic epithelial growth factor T790M mutant non-small cell lung cancer who have been treated with epithelial growth factor receptor tyrosine kinase inhibitors. This study is conducted in Korea. About 600 patients will be monitored until the first occurrence of disease progression, withdrawal of consent, failure of follow-up investigation, and death. □ Research Procedures and Information Gathering Items There are no additional procedures performed by participating in this study and information on safety and effectiveness during the administration of Rexhraza will be followed up in routine care situations. The information you will receive when you participate in this study is as follows. * Subject characteristics, including age, gender, and race * T790M Positive Mutation Status Results and Types of Tests Performed and Receptors * a related medical history * a physical examination * disease characteristics * history of chemotherapy * associated concomitant medications * administration of a test drug * Safety and effectiveness * Resistance mechanism in plasma circulation tumor DNA

Keywords

Eligibility

Minimum Age: 19 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Samsung Medical Center, Seoul, , Korea, Republic of

Contact Details

Name: Jin Seok Ahn, MD, PhD

Affiliation: Samsung Medical Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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