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OncoMatch/Clinical Trials/NCT04205552

Neoadjuvant Nivolumab Combination Treatment in Resectable Non-small Cell Lung Cancer Patients

Is NCT04205552 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Nivolumab 10 MG/ML Intravenous Solution and Relatlimab 10 MG/ML Intravenous Solution for nsclc stage ii.

Phase 2RecruitingUniversity Hospital, EssenNCT04205552Data as of May 2026

Treatment: Nivolumab 10 MG/ML Intravenous Solution · Relatlimab 10 MG/ML Intravenous SolutionThe primary objective of this study is to determine the feasibility of four weeks of preoperative immunotherapy with Nivolumab, and Nivolumab plus Relatlimab in patients with early stage or locally advanced non-small cell lung cancer eligible for curative resection.

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Disease stage

Required: Stage I B, II, SELECTED STAGE III A

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: LAG-3 inhibitor

Prior treatment with Lymphocyte-activation gene 3 (LAG-3) targeting Agent

Cannot have received: anti-PD-1 therapy (nivolumab)

Previous treatment with Nivolumab

Cannot have received: other immune checkpoint inhibitor (relatlimab)

Previous treatment with Relatlimab

Cannot have received: preoperative antineoplastic treatment including irradiation

Any other concurrent preoperative antineoplastic treatment including irradiation

Lab requirements

Blood counts

Adequate hematological function parameters

Kidney function

Adequate renal function parameters

Liver function

Adequate hepatic function parameters

Cardiac function

Sufficient cardiac left ventricular defined as left ventricular ejection fraction (LVEF) ≥ 50% documented either by echocardiography or multigated acquisition scan (MUGA)

Adequate hematological, hepatic and renal function parameters; Sufficient cardiac left ventricular defined as left ventricular ejection fraction (LVEF) ≥ 50% documented either by echocardiography or multigated acquisition scan (MUGA)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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