drugset / Trial / NCT02477826

An Investigational Immuno-therapy Trial of Nivolumab, or Nivolumab Plus Ipilimumab, or Nivolumab Plus Platinum-doublet Chemotherapy, Compared to Platinum Doublet Chemotherapy in Patients With Stage IV Non-Small Cell Lung Cancer (NSCLC)

NCT02477826 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to show that Nivolumab, or Nivolumab plus Ipilimumab, or Nivolumab plus Platinum-Doublet Chemotherapy improves progression free survival and/or overall survival compared with chemotherapy in patients with advanced lung cancer.

Timeline

Start
2015-08-05
Primary completion
2024-10-25
Completion
2024-10-25

Outcome

Mixed primary results

registry analysis (superiority test); Part 1-Arm B: Nivo + Ipi vs Part 1-Arm C: Chemotherapy; Hazard Ratio (HR) 0.79 (95% CI 0.67 to 0.93) NCT02477826 ↗

registry analysis (superiority test); Part 1-Arm A: Nivolumab vs Part 1-Arm C: Chemotherapy; Hazard Ratio (HR) 0.95 (95% CI 0.81 to 1.12) NCT02477826 ↗

registry analysis (superiority test); Part 3 -Arm J: Nivolumab + Ipilimumab vs Part 3 -Arm K: Chemotherapy; Hazard Ratio (HR) 0.85 (95% CI 0.64 to 1.14) NCT02477826 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule — Intravenous
Subject Cisplatin Other / unclassified — Intravenous
Subject Gemcitabine Small molecule — Intravenous
Subject Ipilimumab Monoclonal antibody — Intravenous
Subject Nivolumab Monoclonal antibody — Intravenous
Subject Paclitaxel Small molecule — Intravenous
Subject Pemetrexed Small molecule — Intravenous