Vorolanib + Atezolizumab as Maintenance Therapy for Extensive-Stage Small Cell Lung Cancer
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Washington University School of Medicine
- Study ID
- NCT04373369
- Phase
- PHASE2
- Status
- Terminated
Conditions
- Extensive-stage Small Cell Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Vorolanib — DRUGVorolanib is administered orally at a dose of 200 mg on Days 1 through 21 of each 21-day cycle.
- Atezolizumab — DRUGAtezolizumab is administered intravenously at a dose of 1200 mg on Day 1 of each 21-day cycle.
Study Details
The purpose of the study is to determine whether adding vorolanib to atezolizumab will improve the length of time that participants are cancer-free after receiving standard chemotherapy.
Key Dates
- Start date
- Oct 7, 2020
- Status verified
- Oct 2025
- Primary completion
- Aug 18, 2022
- Completion
- Aug 11, 2025
Study Design
- Enrollment
- 11 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Vorolanib + AtezolizumabConsenting and eligible participants who have no evidence of tumor progression after 3 to 4 cycles of standard-of-care induction therapy will receive atezolizumab intravenously (IV) every 3 weeks and vorolanib by mouth daily.
Primary Outcome Measure
Kaplan Meier Estimate of Progression-free Survival (PFS) at 6 Months [ Time Frame: 6 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Washington University School of Medicine | St Louis | Missouri | 63110 | - |
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