Clinical Trials Directory

Trials / Approved For Marketing

Approved For MarketingNCT04829422

Early Access Program of Lazertinib in Republic of Korea

Multi-center, Prospective, Early Access Program of Lazertinib in Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) Patients With T790M Mutation-positive After 1st/2nd Generation EGFR TKIs Therapy to Assess the Safety and Efficacy of Real World Evidence.

Status
Approved For Marketing
Phase
Study type
Expanded Access
Enrollment
Sponsor
Yuhan Corporation · Industry
Sex
All
Age
19 Years
Healthy volunteers

Summary

This early access program will be conducted to provide access to Lazertinib for adult patients with locally advanced or metastatic Non-small Cell Lung Cancer (NSCLC) with T790M mutation-positive after 1st/2nd generation EGFR TKIs Therapy.

Detailed description

Lazertinib is an oral, highly potent, mutant-selective and irreversible EGFR Tyrosine-kinase inhibitors (TKIs) targets both the T790M mutation and activating EGFR mutations while sparing wild type-EGFR. This is a Multi-center, Prospective, Early Access Program of Lazertinib in locally advanced or metastatic Non-small Cell Lung Cancer (NSCLC) patients with T790M mutation-positive after 1st/2nd generation EGFR TKIs therapy to assess the safety and efficacy of real world evidence as second-line treatment.

Conditions

Interventions

TypeNameDescription
DRUGLazertinib 240 mgThe initial dose of lazertinib 240 mg (3 tablets of 80 mg lazertinib) once daily can be reduced to 160 mg once daily (2 tablets of 80 mg lazertinib) under specific circumstances

Timeline

First posted
2021-04-02
Last updated
2022-03-03

Source: ClinicalTrials.gov record NCT04829422. Inclusion in this directory is not an endorsement.