drugset / Trial / NCT07507188

Collaborative Clinical-translational Cohort of Amivantamab Plus Lazertinib and Amivantamab Plus Chemotherapy in Patients With EGFR-mutant, Locally Advanced or Metastatic/Recurrent Non-Small Cell Lung Cancer (INSTAR Study)

NCT07507188

Phase 2 Not yet recruiting 80 enrolled Yonsei University
Non-randomizedSingle-groupOpen-labelTreatment

Summary

* In this study, we hypothesized that immune engagement by amivantamab will enhance antitumor efficacy by modulating the immune microenvironment in combination with lazertinib in patients with untreated EGFR-mutant NSCLC or with chemotherapy (carboplatin plus pemetrexed) after progression with 3rd generation (3G) EGFR TKI. * The primary objective of this study is to examine the patients' tumors for immunomodulatory effects of amivantamab-based regimens. * In a phase 2, two cohort clinical trial, treatment naïve patients with EGFR-mutant NSCLC will be treated with amivantamab SC plus oral lazertinib (Cohort 1, n=30) or patients with EGFR-mutant NSCLC progressed on or after 3G EGFR TKI treated with amivantamab SC plus chemotherapy (Cohort 2, n=30).

Timeline

Start
2026-04-06
Primary completion
2031-01-31
Completion
2031-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Amivantamab Monoclonal antibody 1600 mg Subcutaneous
Subject Amivantamab Monoclonal antibody 2240 mg Subcutaneous
Subject Amivantamab Monoclonal antibody 2400 mg Subcutaneous
Subject Amivantamab Monoclonal antibody 3360 mg Subcutaneous
Subject Carboplatin Small molecule Intravenous
Subject Lazertinib Small molecule 240 mg Oral
Subject Pemetrexed Small molecule 500 mg/m2 Intravenous