A Study of Atezolizumab Plus Carboplatin and Etoposide With or Without Tiragolumab in Patients With Untreated Extensive-Stage Small Cell Lung Cancer

Part of paid clinical trials in Lone Tree, Colorado.

Sponsor
Hoffmann-La Roche
Study ID
NCT04256421
Phase
PHASE3
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Tiragolumab — DRUG
    Tiragolumab 600 milligrams (mg) administered by IV infusion on Day 1 of each 21-day cycle.
  • Atezolizumab — DRUG
    Atezolizumab 1200 mg administered by IV infusion on Day 1 of each 21-day cycle.
  • Carboplatin — DRUG
    Carboplatin was administered by IV infusion on Day 1 of each 21-day cycle for 4 cycles.
  • Etoposide — DRUG
    Etoposide 100 mg/m\^2 administered by IV infusion on Days 1, 2 and 3 of each 21-day cycle for 4 cycles.
  • Placebo — DRUG
    Placebo administered by IV infusion on Day 1 of each 21-day cycle.

Study Details

This study will evaluate the efficacy of tiragolumab plus atezolizumab and carboplatin and etoposide (CE) compared with placebo plus atezolizumab and CE in participants with chemotherapy-naive extensive-stage small cell lung cancer (ES-SCLC). Eligible participants will be stratified by Eastern Cooperative Oncology Group (ECOG) Performance Status (0 vs. 1), LDH (\</= upper limit of normal \[ULN\] vs. \> ULN), and presence or history of brain metastasis (yes vs. no) and randomly assigned in a 1:1 ratio to receive one of the following treatment regimens during induction phase: * Arm A: Tiragolumab plus atezolizumab plus CE * Arm B: Placebo plus atezolizumab plus CE Following the induction phase, participants will continue maintenance therapy with either atezolizumab plus tiragolumab (Arm A) or atezolizumab plus placebo (Arm B).

Key Dates

Start date
Feb 4, 2020
Status verified
Mar 2026
Primary completion
Sep 6, 2022
Completion
Jul 31, 2025

Study Design

Enrollment
490 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Placebo + Atezolizumab + CE
    Participants will receive atezolizumab on Day 1 of each 21-day cycle followed by placebo on Day 1 of each 21-day cycle. Carboplatin will be administered followed by etoposide on Day 1 for 4 cycles. Participants will also receive etoposide on Days 2 and 3.
  • Experimental: Tiragolumab + Atezolizumab + CE
    Participants will receive atezolizumab on Day 1 of each 21-day cycle followed by tiragolumab on Day 1 of each 21-day cycle. Carboplatin will be administered followed by etoposide on Day 1 for 4 cycles. Participants will also receive etoposide on Days 2 and 3.

Primary Outcome Measure

Investigator-assessed Progression-free Survival (PFS) in the Primary Analysis Set (PAS) [ Time Frame: From randomization to the first occurrence of PD or death from any cause, whichever occurred first (up to approximately 24 months) ]

Locations (18)

FacilityCityStateZIPSite coordinators
Rocky Mountain Cancer Centers - Lone TreeLone TreeColorado80124-
MedStar Georgetown University Hospital (Lombardi Comprehensive Cancer Center)Washington D.C.District of Columbia20007-
Florida Cancer SpecialistsFort MyersFlorida33901-
SCRI Florida Cancer Specialists NorthSarasotaFlorida34232-
Northwest Georgia Oncology Centers PC - MariettaMariettaGeorgia30060-
Illinois Cancer CarePeoriaIllinois61615-
New England Cancer SpecialistsScarboroughMaine04074-
Weinberg Cancer Institution at Franklin SquareBaltimoreMaryland21237-
Minnesota Oncology HematologyMinneapolisMinnesota55404-
Comprehensive Cancer Centers of NevadaHendersonNevada89052-
Broome Oncology - BinghamtonBinghamtonNew York13905-
Memorial Sloan Kettering Cancer CenterNew YorkNew York10065-
Sarah Cannon Research Institute / Tennessee OncologyChattanoogaTennessee37404-
Sarah Cannon Research Inst.NashvilleTennessee37203-
Texas Oncology Cancer CenterAustinTexas78731-
Virginia Cancer SpecialistsFairfaxVirginia22031-
Blue Ridge Cancer CareRoanokeVirginia24014-
University of Wisconsin School of Medicine and Public HealthMadisonWisconsin53792-

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