drugset / Trial / NCT02352948

A Global Study to Assess the Effects of MEDI4736 (Durvalumab), Given as Monotherapy or in Combination With Tremelimumab Determined by PD-L1 Expression Versus Standard of Care in Patients With Locally Advanced or Metastatic Non Small Cell Lung Cancer

NCT02352948

Phase 3 Completed 597 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a Phase III, randomised, open label, multi-centre study assessing the efficacy and safety of MEDI4736 (durvalumab) versus Standard of Care in NSCLC patients with PD-L1 positive tumours and the combination of MEDI4736 (durvalumab) plus tremelimumab (MEDI4736+treme) versus Standard of Care in NSCLC patients with PD-L1-negative tumours in the treatment of male and female patients with locally advanced or metastatic NSCLC (Stage IIIB-IV), who have received at least 2 prior systemic treatment regimens including 1 platinum-based chemotherapy regimen for NSCLC. Patients with known EGFR (Epidermal growth factor receptor) tyrosine kinase (TK) activating mutations and anaplastic lymphoma kinase (ALK) rearrangements are not eligible for the study (prospective testing is not planned within this study). The Standard of Care options are: an EGFR tyrosine kinase inhibitor (erlotinib \[TARCEVA®\]), gemcitabine or vinorelbine (NAVELBINE®)

Timeline

Start
2015-01-13
Primary completion
2018-02-09
Completion
2023-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 10 mg/kg Intravenous
Comparator Erlotinib Small molecule 150 mg Oral
Comparator Gemcitabine Small molecule 1000 mg/m2 Intravenous
Subject Tremelimumab Monoclonal antibody 1 mg/kg Intravenous
Subject Tremelimumab Monoclonal antibody 10 mg/kg Intravenous
Comparator Vinorelbine Small molecule 30 mg/m2 Intravenous