CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 28 enrolled
Drug / intervention
Atezolizumabdrug
Likely dose
Atezolizumab 1200mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03014648
NCT03014648Phase 2Completed

A Phase II Clinical Trial Evaluating the Efficacy of Atezolizumab in Advanced Non-small Cell Lung Cancer (NSCLC) in Patients Previously Treated With PD-1-directed Therapy

Liza Villaruz, MD·interventional·Posted Jan 9, 2017·Updated Dec 13, 2023

In Brief

A Phase 2 clinical trial evaluating Atezolizumab for Advanced Non-small Cell Lung Cancer. Completed, enrolled 28 participants across 2 sites.

Detailed 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)

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsGenentech, Inc.

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedJan 9, 2017
Enrollment StartJul 18, 2017
Primary CompletionDec 31, 2021
Study CompletionMar 31, 2022
TodayJul 2, 2026
Enrollment to primary: 4.5 yearsPosted 9.5 years ago

Interventions

Atezolizumabdrug

Atezolizumab will be administered through an IV over 60 minutes at a dose of 1200mg on Day 1 of each 21-day cycle. If the first dose is tolerated without any infusion-related adverse events, the following doses can be administered over 30 minutes.