drugset / Trial / NCT02250326

Safety and Efficacy Study of Nab®-Paclitaxel With CC-486 or Nab®-Paclitaxel With Durvalumab, and Nab®-Paclitaxel Monotherapy as Second/Third-line Treatment for Advanced Non-small Cell Lung Cancer

NCT02250326 ↗

Phase 2 Completed 240 enrolled Celgene Corporation
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 2, open-label, multicenter study to assess the efficacy and safety of second/third-line treatment with nab-paclitaxel in combination with the epigenetic modifying therapy of CC-486 or immunotherapy of durvalumab, and nab-paclitaxel monotherapy in subjects with advanced non-small cell lung cancer (NSCLC).

Timeline

Start
2015-01-07
Primary completion
2017-07-17
Completion
2023-08-17

Outcome

Missed primary endpoint

registry analysis (superiority test); Nab-Paclitaxel + CC-486 vs Nab-Paclitaxel Alone; Hazard Ratio (HR) 1.3 (95% CI 0.90 to 1.94) NCT02250326 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CC-486 Unknown 200 mg Oral
Subject Durvalumab Monoclonal antibody 1125 mg Intravenous
Subject Nab-paclitaxel Small molecule 100 mg/m2 Intravenous