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Completed Phase 3 Interventional Results available

A Study of Carboplatin Plus Etoposide With or Without Atezolizumab in Participants With Untreated Extensive-Stage (ES) Small Cell Lung Cancer (SCLC)

ClinicalTrials.gov ID: NCT02763579

Public ClinicalTrials.gov record NCT02763579. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 1:51 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I/III, Randomized, Double-Blind, Placebo-Controlled Study of Carboplatin Plus Etoposide With or Without Atezolizumab (Anti-PD-L1 Antibody) in Patients With Untreated Extensive-Stage Small Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, Phase I/III, multicenter, double-blinded, placebo-controlled study was designed to evaluate the safety and efficacy of atezolizumab (anti-programmed death-ligand 1 \[PD-L1\] antibody) in combination with carboplatin plus (+) etoposide compared with treatment with placebo + carboplatin + etoposide in chemotherapy-naive participants with ES-SCLC. Participants will be randomized in a 1:1 ratio to receive either atezolizumab + carboplatin + etoposide or placebo + carboplatin + etoposide on 21-day cycles for four cycles in the induction phase followed by maintenance with atezolizumab or placebo until progressive disease (PD) as assessed by the investigator using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1). Treatment can be continued until persistent radiographic PD or symptomatic deterioration.

Study identification

NCT ID
NCT02763579
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
503 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 7, 2016 (Actual)
Primary completion
Apr 24, 2018 (Actual)
Completion
Jul 7, 2022 (Actual)
Last update posted
Jul 28, 2023

2016 – 2022

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Florida Cancer Specialists - Fort Myers (Broadway) Fort Myers Florida 33901 —
Florida Hospital Orlando Florida 32804 —
Florida Cancer Specialists. St. Petersburg Florida 33705 —
Northwest Georgia Oncology Centers PC - Marietta Marietta Georgia 30060 —
Rush University Medical Center Chicago Illinois 60612-3244 —
Illinois Cancer Care Peoria Illinois 61615 —
Cancer Treatment Centers of America - Midwestern Regional Medical Center Zion Illinois 60099 —
Louisville Oncology Louisville Kentucky 40202 —
New England Cancer Specialists Scarborough Maine 04074 —
Weinberg CA Inst Franklin Sq Baltimore Maryland 21237 —
Mayo Clinic Rochester Minnesota 55905 —
Comprehensive Cancer Centers of Nevada - Eastern Avenue Las Vegas Nevada 89169 —
The Valley Hospital Paramus New Jersey 07652 —
Broome Oncology - Binghamton Binghamton New York 13905 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Tennessee Oncology Chattanooga Chattanooga Tennessee 37404 —
Tennessee Oncology PLLC - Nashville (20th Ave) Nashville Tennessee 37203 —
Vanderbilt Medical Center Nashville Tennessee 37232-7610 —
Virginia Cancer Specialists, PC Fairfax Virginia 22031 —
Blue Ridge Cancer Care Roanoke Virginia 24014 —
Northwest Medical Specialties Tacoma Washington 98405 —
University of Wisconsin Madison Wisconsin 53705 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 92 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02763579, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 28, 2023 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02763579 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →