drugset / Trial / NCT01903993

A Randomized Phase 2 Study of Atezolizumab (an Engineered Anti-PDL1 Antibody) Compared With Docetaxel in Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer Who Have Failed Platinum Therapy - "POPLAR"

NCT01903993 ↗

Phase 2 Completed 287 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This multicenter, open-label, randomized study will evaluate the efficacy and safety of Atezolizumab compared with docetaxel in participants with advanced or metastatic non-small cell lung cancer after platinum failure. Participants will be randomized to receive either Atezolizumab 1200 milligram (mg) intravenously every 3 weeks or docetaxel 75 milligram per meter square (mg/m\^2) intravenously every 3 weeks. Treatment with Atezolizumab may be continued as long as participants are experiencing clinical benefit as assessed by the investigator, i.e., in the absence of unacceptable toxicity or symptomatic deterioration attributed to disease progression.

Timeline

Start
2013-08-06
Primary completion
2015-11-19
Completion
2018-09-06

Outcome

Met primary endpoint

registry analysis (unspecified test); Docetaxel vs Atezolizumab; p = 0.0106; Hazard Ratio (HR) 0.69 (95% CI 0.52 to 0.92); Log rank (Stratified) NCT01903993 ↗

paper Atezolizumab significantly improved survival compared with docetaxel in patients with previously treated NSCLC. PMID 26970723 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atezolizumab Monoclonal antibody 1200 mg Intravenous
Comparator Docetaxel Small molecule 75 mg/m2 Intravenous