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Adjuvant Nivolumab in Resected Lung Cancers (ANVIL)-A Randomized Phase III Study of Nivolumab After Surgical Resection and Adjuvant Chemotherapy in Non-Small Cell Lung Cancers

Co-Primary Endpoints: To evaluate whether adjuvant therapy with nivolumab will result in improved overall survival (OS) and/or disease-free survival (DFS) over standard observation in patients with Stage IB greater than or equal to 4cm, II and IIIA, NSCLC following surgical resection and standard adjuvant therapy. Secondary Endpoints: To evaluate the safety profile of nivolumab when given as an adjuvant therapy To evaluate and compare disease free and overall survival in patients with tumors that express PD-L1 in various patterns associated with nivolumab and standard observation To evaluate and compare disease free and overall survival in patients with tumors that have high mutational load associated with nivolumab and standard observation To evaluate OS and DFS by stage To evaluate OS and DFS by each stratification factor To evaluate the proportion of patients alive and progression free at 1 year, 2 years, and 5 years (OS and DFS rate)

Phase

III

Recruitment Status

Past Studies