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Study identifier: NCT06449313 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neoadjuvant Chemo-Immunotherapy and Surgical Resection in Locally Advanced Non-small Cell Lung Cancer With N3 Lymph Node Involvement

Condition: Non-small Cell Lung Cancer Stage III  ·  Sponsor: Georgetown University

PhasePhase 2
Planned participants21
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn about neoadjuvant cemiplimab with histology-specific chemotherapy followed by resection and adjuvant cemiplimab in stage 3 non-small cell lung cancer (NSCLC) with contralateral mediastinal or ipsilateral supraclavicular lymph node (N3) involvement.. The main question it aims to answer is whether patients with stage 3 NSCLC with involvement of lymph nodes can undergo surgery to remove the cancer after receiving treatment with chemotherapy + immunotherapy. Participants will receive FDA-approved chemotherapy called platinum-doublet chemotherapy together with an immunotherapy drug targeting the immune marker PD-1 called cemiplimab. Patients will receive a 3 drug combination for 4 total treatments given every 3 weeks before surgery. After surgery, patients will have the option to undergo radiation therapy if it is recommended by their treatment team. After this, they will receive cemiplimab every 3 weeks for one year.

This description comes directly from the study's public registry record.

Talk to the study team

Joshua Reuss, MD  ·  202-444-2223  ·  Joshua.E.Reuss@gunet.georgetown.edu

Always discuss trial participation with your own doctor first.

Locations (3)

Lombardi Comprehensive Cancer Center, Georgetown UniversityWashington D.C., District of Columbia, United StatesRecruiting
Washington University School of Medicine-Sitemen Cancer CenterSt Louis, Missouri, United StatesRecruiting
UVA Comprehensive Cancer CenterCharlottesville, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06449313