Combinations of Cemiplimab (Anti-PD-1 Antibody) and Platinum-based Doublet Chemotherapy in Patients With Lung Cancer
Фаза 3
Завершено
NCT03409614
| Заболевание | Non-small Cell Lung Cancer |
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| Фаза | Фаза 3 |
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| Спонсор | Regeneron Pharmaceuticals |
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| Статус | Завершено |
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| Участники | 789 участн. |
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| Вмешательство | REGN2810, REGN2810/chemo/ipi, Chemotherapy |
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| Дата начала | 6.03.2018 |
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| Дата завершения | 27.02.2025 |
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| Публикация результатов | 29.04.2026 |
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Кратко
The primary objectives of this study are: Part 1: To compare the overall survival (OS) of cemiplimab/chemo-f and cemiplimab/chemo-l/ipi versus platinum-based doublet chemotherapy in the first-line treatment of patients with advanced squamous or nonsquamous non-small cell lung cancer (NSCLC) with tumors expressing PD-L1 in \<50% of tumor cells. Part 2: To compare the OS of cemiplimab/chemo-f with placebo/chemo-f in the first-line treatment of patients with advanced squamous or non-squamous NSCLC irrespective of PD-L1 expression. The key secondary objectives are: Part 1: To compare the progression-free survival (PFS) and objective response rate (ORR) of cemiplimab/chemo-f and cemiplimab/chemo-l/ipi versus chemo-f in the first-line treatment of patients with advanced squamous or non-squamous NSCLC and tumors expressing PD-L1 in \<50% of tumor cells. Part 2: To compare the PFS and ORR of cemiplimab/chemo-f versus placebo/chemo-f in the first-line treatment of patients with advanced squamous or non-squamous NSCLC irrespective of PD-L1 expression.
Part 1: Overall Survival (OS)
Up to a maximum of 82.2 months · months
| Part 1: Cemiplimab + Chemotherapy | 15.9 months |
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| Part 1: Cemiplimab+AbbrevChemo+Ipilimumab | 20.1 months |
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| Part 1: Chemotherapy | 13.9 months |
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| p-value | 0.1782 |
| Hazard Ratio (HR) | 0.813 (95% CI 0.601–1.100) |
Part 2: OS
Up to a maximum of 68.4 months · months
| Part 2: Cemiplimab + Chemotherapy | 21.1 months |
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| Part 2: Placebo + Chemotherapy | 12.9 months |
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| p-value | 0.0002 |
| Hazard Ratio (HR) | 0.662 (95% CI 0.531–0.825) |
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