Data from Clinicaltrials.gov - Curated by EPG Health - Last updated 04 October 2017

This global, multicenter, open-label, randomized, controlled study will evaluate the efficacy and safety of atezolizumab (an anti-programmed death−ligand 1 [anti-PD-L1] antibody) compared with docetaxel...

purpose

This global, multicenter, open-label, randomized, controlled study will evaluate the efficacy and safety of atezolizumab (an anti-programmed death−ligand 1 [anti-PD-L1] antibody) compared with docetaxel in participants with locally advanced or metastatic non-small cell lung cancer (NSCLC) after failure with platinum-containing chemotherapy. Participants will be randomized 1:1 to receive either docetaxel or atezolizumab. Treatment may continue 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.


Study Type: Interventional
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase III, Open-Label, Multicenter, Randomized Study to Investigate the Efficacy and Safety of Atezolizumab (Anti-PD-L1 Antibody) Compared With Docetaxel in Patients With Non-Small Cell Lung Cancer After Failure With Platinum Containing Chemotherapy
Enrollment: 1225
Actual Study Start Date: March 11, 2014
Estimated Study Completion Date: December 31, 2018
Primary Completion Date: July 7, 2016 (Final data collection date for primary outcome measure)

Arms:
- Experimental:
Atezolizumab (MPDL3280A), an Engineered Anti-PD-L1 Antibody
- Active Comparator: Docetaxel


Related journal:
- Atezolizumab versus docetaxel in patients with previously treated non-small-cell lung cancer (OAK): a phase 3, open-label, multicentre randomised controlled trial.

Category Value
Date last updated at source 02-Jul-17
Study type(s) Interventional
Expected enrolment 1225
Study start date 11-Mar-17
Estimated primary completion date 07-Jul-16

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