278
Participants
Start Date
May 15, 2025
Primary Completion Date
December 31, 2027
Study Completion Date
December 31, 2028
Vebreltinib
Subjects will receive Vebreltinib Enteric-coated Capsule orally twice per day (BID).
PLB1004
Subjects will receive PLB1004 80mg orally once per day (QD).
Pemetrexed plus Carboplatin or Cisplatin
Subjects randomized to the control group received pemetrexed 500 mg/m² + platinum-based chemotherapy (carboplatin AUC 5 or cisplatin 75 mg/m²) via intravenous infusion for 4-6 cycles (determined by the investigator) as initial therapy, followed by pemetrexed maintenance therapy (500 mg/m²) until disease progression, intolerable toxicity, initiation of new antitumor therapy, death, loss to follow-up, or other treatment-terminating conditions (whichever occurred first).
Avistone Biotechnology Co., Ltd.
INDUSTRY