drugset / Trial / NCT01642004

Study of BMS-936558 (Nivolumab) Compared to Docetaxel in Previously Treated Advanced or Metastatic Squamous Cell Non-small Cell Lung Cancer (NSCLC) (CheckMate 017)

NCT01642004 ↗

Phase 3 Completed 272 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to compare the overall survival of BMS-936558 as compared with Docetaxel in subjects with squamous cell non-small cell lung cancer (NSCLC), after failure of prior platinum-based chemotherapy.

Timeline

Start
2012-10-16
Primary completion
2014-11-17
Completion
2021-08-16

Outcome

Met primary endpoint

registry Nivolumab vs Docetaxel; p = 0.0002; Hazard Ratio (HR) 0.59 (96.85% CI 0.43 to 0.81) NCT01642004 ↗

paper The risk of death was 41% lower with nivolumab than with docetaxel (hazard ratio, 0.59; 95% CI, 0.44 to 0.79; P<0.001). PMID 26028407 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 75 mg/m2 Intravenous
Subject Nivolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 480 mg Intravenous