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Active, Not Recruiting

A Study of Relatlimab Plus Nivolumab in Combination With Chemotherapy vs. Nivolumab in Combination With Chemotherapy as First Line Treatment for Participants With Stage IV or Recurrent Non-small Cell Lung Cancer (NSCLC) - CA224-104

Updated: 5 June, 2024   |   ClinicalTrials.gov

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Trial Details

  • Phase 2

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Part 1: Arm A (Nivolumab + Relatlimab Dose 1 + Platinum Doublet Chemotherapy (PDCT))
Biological: Nivolumab, Relatlimab Drug: Carboplatin, Cisplatin, Paclitaxel, Nab-Paclitaxel, Pemetrexed
Experimental: Part 1: Arm B (Nivolumab + Relatlimab Dose 2 + PDCT))
Biological: Nivolumab, Relatlimab Drug: Carboplatin, Cisplatin, Paclitaxel, Nab-Paclitaxel, Pemetrexed
Experimental: Part 2: Arm C (Nivolumab + Relatlimab Dose 2 + PDCT)
Biological: Nivolumab, Relatlimab Drug: Carboplatin, Cisplatin, Paclitaxel, Pemetrexed
Active Comparator: Part 2: Arm D (Nivolumab + PDCT)
Biological: Nivolumab Drug: Carboplatin, Cisplatin, Paclitaxel, Pemetrexed

Key Eligibility Criteria

Inclusion Criteria - Histologically confirmed metastatic non-small cell lung cancer (NSCLC) of squamous (SQ) or non-squamous (NSQ) histology with Stage IV A/B (as defined by the 8th International Association for the Study of Lung Cancer Classification) or recurrent disease following multi-modal therapy for locally advanced disease. - Eastern Cooperative Oncology Group (ECOG) performance status (PS) of less than or equal to 1 at screening and confirmed prior to randomization. - Measurable disease by computed tomography (CT) or magnetic resonance resources (MRI) per response evaluation criteria in solid tumor version 1.1 (RECIST 1.1) criteria. - No prior systemic anti-cancer treatment (including epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) inhibitors) given as primary therapy for advanced or metastatic disease. Exclusion Criteria - Participants with EGFR, ALK, ROS-1, or known B-rapidly accelerated fibrosarcoma proto-oncogene (BRAF V600E) mutations that are sensitive to available targeted therapy. - Untreated CNS metastases. - Leptomeningeal metastases (carcinomatous meningitis). - Concurrent malignancy requiring treatment or history of prior malignancy active within 2 years prior to randomization (ie, participants with a history of prior malignancy are eligible if treatment was completed at least 2 years before randomization and the participant has no evidence of disease). - Prior treatment with an anti-programmed cell death protein 1 (PD-1), anti-programmed death-ligand 1 (PD-L1), anti-programmed death-ligand 2 (PD-L2), or anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antibody, or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways. - Other protocol-defined Inclusion/Exclusion criteria apply.

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