A Study of Tiragolumab in Combination With Atezolizumab in Chemotherapy-Naïve Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer
Part of paid clinical trials in Tempe, Arizona.
- Sponsor
- Genentech, Inc.
- Study ID
- NCT03563716
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Atezolizumab — DRUGAtezolizumab at a fixed dose of 1200 mg will be administered first by IV infusion Q3W on Day 1 of each 21-day cycle.
- Tiragolumab — DRUGTiragolumab at a fixed dose of 600 mg will be administered by IV infusion Q3W on Day 1 of each 21-day cycle.
- Placebo — DRUGPlacebo will be administered by IV infusion Q3W on Day 1 of each 21-day cycle.
Study Details
This study will evaluate the safety and efficacy of tiragolumab plus atezolizumab compared with placebo plus atezolizumab in chemotherapy-naive patients with locally advanced unresectable or metastatic PD-L1-selected non-small cell lung cancer (NSCLC), excluding patients with a sensitizing EGFR mutation or ALK translocation.
Key Dates
- Start date
- Aug 10, 2018
- Status verified
- Apr 2026
- Primary completion
- Jun 30, 2019
- Completion
- Nov 14, 2025
Study Design
- Enrollment
- 135 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Placebo Comparator: Placebo + AtezolizumabParticipants will receive atezolizumab at a fixed dose of 1200 mg administered by IV infusion Q3W on Day 1 of each 21-day cycle and placebo administered by IV infusion Q3W on Day 1 of each 21-day cycle.
- Experimental: Tiragolumab + AtezolizumabParticipants will receive atezolizumab at a fixed dose of 1200 mg administered by intravenous (IV) infusion every 3 weeks (Q3W) on Day 1 of each 21-day cycle and tiragolumab at a dose of 600 mg administered by IV infusion Q3W on Day 1 of each 21-day cycle.
Primary Outcome Measure
Objective Response Rate (ORR) [ Time Frame: From baseline until a total of 80 progression-free survival (PFS) events have occurred (up to approximately 11 months) ]
Locations (11)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Arizona Oncology Associates, PC - HAL | Tempe | Arizona | 85284 | - |
| SCRI Florida Cancer Specialists South | Fort Myers | Florida | 33901 | - |
| Florida Cancer Specialists - NORTH - SCRI - PPDS | St. Petersburg | Florida | 33705 | - |
| Illinois Cancer Specialists | Arlington Heights | Illinois | 60005 | - |
| Illinois Cancer Care | Peoria | Illinois | 61615 | - |
| University of Kansas Medical Center | Westwood | Kansas | 66205 | - |
| Karmanos Cancer Institute | Detroit | Michigan | 48201 | - |
| Research Medical Center | Kansas City | Missouri | 64132 | - |
| SCRI Tennessee Oncology | Nashville | Tennessee | 37203 | - |
| Virginia Cancer Specialists, PC | Fairfax | Virginia | 22031 | - |
| Northwest Cancer Specialists - Vancouver | Vancouver | Washington | 98684 | - |
Find similar trials in Tempe, AZ
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Arizona Oncology Associates, PC - HAL· Tempe, AZSCRI Florida Cancer Specialists South· Fort Myers, FLFlorida Cancer Specialists - NORTH - SCRI - PPDS· St. Petersburg, FLIllinois Cancer Specialists· Arlington Heights, ILIllinois Cancer Care· Peoria, ILUniversity of Kansas Medical Center· Westwood, KS
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