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A Phase II Study for the Evaluation of the Feasibility of Lazertinib 160mg Per Day in Patients With EGFR T790M Mutant Non-small Cell Lung Cancer
The lazertinib is currently approved as 2nd line T790M mutation-positive NSCLC that failed from either 1st or 2nd generation EGFR TKI. The current recommended dosage is 240mg. Based on the promising clinical efficacy of the dose escalation study, this study is designed to evaluatee the clinical efficacy and safety of 160mg lazertinib.
Age
19 - No limit years
Sex
ALL
Healthy Volunteers
No
Samsung Medical Center
Seoul, MA, South Korea
Start Date
February 1, 2023
Primary Completion Date
January 31, 2024
Completion Date
January 31, 2025
Last Updated
January 27, 2023
117
ESTIMATED participants
Lazertinib
DRUG
Lead Sponsor
Samsung Medical Center
NCT07250477
NCT06639191
Data Source & Attribution
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