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Clinical Trial Summary

The goal of this clinical trial] is to learn about neoadjuvant cemiplimab with histology-specific chemotherapy followed by resection and adjuvant cemiplimab in stage III non-small cell lung cancer (NSCLC) with contralateral mediastinal or ipsilateral supraclavicular lymph node 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06449313
Study type Interventional
Source Georgetown University
Contact Joshua Reuss, MD
Phone 202-444-2223
Email Joshua.E.Reuss@gunet.georgetown.edu
Status Not yet recruiting
Phase Phase 2
Start date September 2024
Completion date September 2032

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