Extracted Trials
Select a trial for this version to view the audit.

NCT04025879

CheckMate 816

Leal TA et al. (2022)

Eligibility Criteria

Inclusion Criteria

Participants with suspected or histologically confirmed Stage IIA (> 4 cm) to IIIB (T3N2) non-small cell lung carcinoma (NSCLC) with disease that is considered resectable No brain metastasis Treatment-naive for NSCLC (no prior systemic anti-cancer treatment) Ability to provide surgical or biopsy tumor tissue for biomarkers Eastern Cooperative Oncology Group (ECOG) Performance Status of ≤ 1

Exclusion Criteria

Participants with an active, known or suspected autoimmune disease Any positive test for hepatitis B virus or hepatitis C virus or human immunodeficiency virus (HIV) Any previous anti-cancer treatment including cytotoxic, IO treatment, targeted agents, or radiotherapy for NSCLC Prior treatment with any anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways

Bibliographic Info
Trial Acronym:
CheckMate 816
First Author:
Leal TA
Year:
2022
PMID:
35858590
View Article
Patient Baseline
N (Intervention):
229
N (Control):
232
Intervention Details

Clinical Endpoints

Built with v0