Stereotactic Body Radiotherapy (SBRT) Plus Immunotherapy for Cancer
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Chicago
- Study ID
- NCT03431948
- Phase
- PHASE1
- Status
- Completed
Conditions
- Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab — DRUGNivolumab 240 mg given by intravenous infusion every 2 weeks
- Cabiralizumab — DRUGCabiralizumab 4 mg/kg given by intravenous infusion every 2 weeks
- Urelumab — DRUGUrelumab 8 mg given by intravenous infusion every 4 weeks
- Stereotactic Body Radiation Therapy — RADIATIONRadiation to metastatic lesion(s) given at assigned dose levels based on lesion location and dose level being tested at time of enrollment. Doses range from 30 - 50 Gy.
Study Details
Study to determine the best dose of stereotactic body radiation therapy (SBRT) to be administered in combination with immunotherapy drugs including urelumab, cabiralizumab and nivolumab .
Key Dates
- Start date
- Mar 15, 2018
- Status verified
- Feb 2023
- Primary completion
- Feb 29, 2020
- Completion
- Apr 11, 2022
Study Design
- Enrollment
- 60 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: SBRT with Nivolumab and UrelumabPatients will receive stereotactic body radiation therapy (SBRT) in combination with nivolumab and urelumab.
- Experimental: SBRT with Nivolumab and CabiralizumabPatients will receive stereotactic body radiation therapy (SBRT) in combination with nivolumab and cabiralizumab .
Primary Outcome Measure
Recommended dose of SBRT given in combination with immunotherapy [ Time Frame: 3 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago Medical Center | Chicago | Illinois | 60637 | - |
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