To assess the safety and efficacy of third-line and above therapy of patients with local advanced or metastatic non-small cell lung cancer (NSCLC) with combined treatment with launched recombinant humanized anti-PD-1 monoclonal antibody and Donafenib Tosilate
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
safety assessments
Timeframe: From signing ICF to 30 days after the end of treatment