Vebreltinib Plus PLB1004 Versus Platinum-based Doublet Chemotherapy in Patients With EGFRm, MET+, Locally Advanced or Metastatic NSCLC Following EGFR-TKI Failure

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorAvistone Biotechnology Co., Ltd.

About this trial

Efficacy and Safety of Vebreltinib in Combination With PLB1004 Versus Platinum-based Doublet Chemotherapy in Patients With EGFR Mutations, MET Amplification and/or Overexpression, Locally Advanced or Metastatic Non-Small Cell Lung Cancer Following EGFR-TKI Treatment Failure

Eligibility criteria

Qualifiers

Ability to understand and willingness to sign a written informed consent document.

Aged at least 18 years old.

Histologically or cytologically confirmed locally advanced or metastatic NSCLC (stage IIIB~IV).

At least one measurable lesion as defined by RECIST V1.1.

Disqualifiers

There are mutations of ALK or ROS1.

Have symptomatic and neurologically unstable central nervous system (CNS) metastases or CNS disease that requires increased steroid doses for control.

Before randomization, patients did not recover from any toxicity and/ or complications of previous chemotherapy, surgery, radiotherapy and other anti-cancer treatments, that is, did not fall to grade 1 or lower (National Cancer Research Common Toxicity Criteria for Adverse Events [NCI-CTCAE] v5.0), except for hair loss and irrecoverable permanent radiation damage.

Major surgery or had significant traumatic injury within 4 weeks prior to the first dose of the investigational product.

Trial design

Treatments tested in this trial

  • Vebreltinib
  • PLB1004
  • Pemetrexed plus Carboplatin or Cisplatin

Treatment groups

278 Participants
are divided into 2 treatment groups

Locations

This trial has no locations