ASKC202 Combined With Limertinib Versus Platinum-based Chemotherapy in Treatment of Locally Advanced or Metastatic NSCLC With MET Amplification/Overexpression After Failure of EGFR-TKI Therapy

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorJiangsu Aosaikang Pharmaceutical Co., Ltd.

About this trial

This study is designed to compare the safety and efficacy of ASKC202 combined with Limertinib Versus platinum-based chemotherapy in locally advanced or metastatic NSCLC With MET Amplification/Overexpression after disease progression on EGFR tyrosine kinase inhibitor.

Eligibility criteria

Qualifiers

Willing and able to provide signed and dated informed consent;

Patients at least 18 years of age;

Locally advanced or metastatic non-small cell lung cancer (NSCLC);

Objective disease progression following prior EGFR-TKI therapy;

Disqualifiers

Prior or ongoing treatment with any c-Met target;

Previously received systemic chemotherapy;

Patients requiring continuous use of systemic immunosuppressants or systemic corticosteroids within 2 weeks prior to the first dose.

Patients who underwent other major surgical procedures other than diagnosis or biopsy within 4 weeks prior to the first dose, or who were expected to undergo major surgeries during the study period;

Trial design

Treatments tested in this trial

  • ASKC202+ Limertinib
  • Pemetrexed + Cisplatin /Carboplatin

Treatment groups

286 Participants
are divided into 2 treatment groups