Lazertinib for NSCLC Harboring Activating EGFR Mutations in TKI naïve Patients

NCT05463224 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2026-04-28

No results posted yet for this study

Summary

The primary objective is to evaluate the efficacy/safety of lazertinib and to explore the resistance mechanism of lazertinib as first-line in patients with NSCLC harboring activating EGFR mutations.

Conditions

Interventions

DRUG

Lazertinib group

Lazertinib 240mg, Once, po, daily (1 cycle of 21 days)

Sponsors & Collaborators

  • Se-Hoon Lee

    lead OTHER

Principal Investigators

  • Se-Hoon Lee, MD · Samsung Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-04
Primary Completion
2026-12-01
Completion
2027-12-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05463224 on ClinicalTrials.gov