Impact of Lazertinib Dose Modification on Effectiveness and Safety

Not yet recruitingOBSERVATIONAL
Enrollment

200

Participants

Timeline

Start Date

February 1, 2023

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Non-small Cell Lung Cancer
Interventions
DRUG

Lazertinib

Lazertinib 240mg(3tablets, 80mg/1tablet), once a day(QD), oral(PO), until disease progression or unacceptable toxicity

Trial Locations (11)

41404

Kyungpook National University Chilgok Hospital, Daegu

41944

Kyungpook National University Hospital, Daegu

42415

Yeungnam University Medical Center, Daegu

42472

Daegu Catholic University Medical Center, Daegu

42601

Keimyung University Dongsan Medical Center, Daegu

47392

Inje University Busan Paik Hospital, Busan

48108

Inje University Haeundae Paik Hospital, Busan

49201

Dong-A University Hospital, Busan

49241

Pusan National University Hospital, Busan

49267

Kosin University Gospel Hospital, Busan

50612

Pusan National University Yangsan Hospital, Yangsan

All Listed Sponsors
collaborator

Yuhan Corporation

INDUSTRY

lead

Pusan National University Hospital

OTHER

NCT05716672 - Impact of Lazertinib Dose Modification on Effectiveness and Safety | Biotech Hunter | Biotech Hunter