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Clinical Trial Summary

This is a phase II clinical trial aimed at evaluating the efficacy of PD-L1 inhibition with atezolizumab in advanced squamous and non-squamous NSCLC patients previously treated with anti-PD-1 therapy with either nivolumab or pembrolizumab. In order to account for the variability of response kinetics to PD-1 directed therapy, patients will be enrolled in 3 parallel cohorts based on the best overall response to PD-1 directed therapy. - Cohort 1 (progressive disease) - Cohort 2 (stable disease with minimum 12 weeks of therapy) - Cohort 3 (partial to complete response followed by progressive disease)


Clinical Trial Description

Atezolizumab will be given on day 1 of a 21-day cycle at 1200 mg IV. Radiographic assessments for disease response will occur every 6 weeks while on treatment. Confirmatory scans should be obtained ≥ 4 weeks following initial documentation of objective response or progressive disease on atezolizumab therapy. Atezolizumab will be given as long as the patient continues to experience clinical benefit in the opinion of the investigator or until unacceptable toxicity, symptomatic deterioration attributed to disease progression. Patients will be followed for 12 months or until death as per standard of care after discontinuation of Atezolizumab or until death, whichever occurs first. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03014648
Study type Interventional
Source University of Pittsburgh
Contact
Status Completed
Phase Phase 2
Start date July 18, 2017
Completion date March 31, 2022

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