36
Participants
Start Date
March 31, 2025
Primary Completion Date
March 31, 2030
Study Completion Date
August 31, 2030
lorlatinib
Eligible patients will be registered to receive oral lorlatinib 100mg qd for 36 months during the treatment phase.
concurrent/sequential platinum-based chemoradiotherapy
The choice of chemotherapy and will be determined by the investigator prior to treatment allocation and the radiotherapy also according to the clinical therapy regimen decided by the investigator.
Guangdong Association of Clinical Trials
OTHER