Testing Ipilimumab and Nivolumab Combination With or Without Cabozantinib in People >= 18 Years Old With Advanced Soft Tissue Sarcoma
Part of paid clinical trials in Duarte, California.
- Sponsor
- National Cancer Institute LAO
- Study ID
- NCT05836571
- Phase
- PHASE2
- Status
- Active Not Recruiting
Conditions
- Locally Advanced Extraskeletal Myxoid Chondrosarcoma
- Locally Advanced Leiomyosarcoma
- Locally Advanced Liposarcoma
- Locally Advanced Undifferentiated Pleomorphic Sarcoma
- Locally Advanced Unresectable Soft Tissue Sarcoma
- Metastatic Soft Tissue Sarcoma
- Metastatic Undifferentiated Pleomorphic Sarcoma
- Unresectable Leiomyosarcoma
- Unresectable Liposarcoma
- Unresectable Undifferentiated Pleomorphic Sarcoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Biopsy Procedure — PROCEDUREUndergo biopsy
- Biospecimen Collection — PROCEDUREUndergo collection of urine and/or blood sample
- Cabozantinib — DRUGGiven PO
- Computed Tomography — PROCEDUREUndergo CT
- Ipilimumab — BIOLOGICALGiven IV
- Magnetic Resonance Imaging — PROCEDUREUndergo MRI
- Nivolumab — BIOLOGICALGiven IV
Study Details
This phase II trial compares the effect of immunotherapy with ipilimumab and nivolumab alone to their combination with cabozantinib in treating patients with soft tissue sarcoma that has spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Immunotherapy with monoclonal antibodies, such as ipilimumab and nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Cabozantinib is in a class of medications called kinase inhibitors. It works by blocking the action of an abnormal protein that signals cancer cells to multiply and may also prevent the growth of new blood vessels that tumors need to grow. By these actions it may help slow or stop the spread of cancer cells. Adding cabozantinib to the combination of ipilimumab and nivolumab may be better in stopping or slowing the growth of tumor compared to ipilimumab and nivolumab alone in patients with advanced soft tissue sarcoma.
Key Dates
- Start date
- Oct 25, 2023
- Status verified
- Apr 2026
- Primary completion
- May 15, 2026
- Completion
- May 15, 2026
Study Design
- Enrollment
- 66 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Arm A (nivolumab, ipilimumab)Patients receive nivolumab IV over 30-60 minutes and ipilimumab IV over 60-90 minutes on day 1 of each cycle. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity for 4 cycles. Patients then receive nivolumab IV over 30 minutes on day 1 of subsequent cycles. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT or MRI scans, tumor biopsies, and collection of urine samples throughout the trial. Patients may also optionally undergo collection of blood samples at baseline. Patients can crossover from Arm A to Arm B at the time of disease progression.
- Experimental: Arm B (cabozantinib, nivolumab, ipilimumab)See Detailed Description.
Primary Outcome Measure
Progression-free survival (PFS) [ Time Frame: Up to 30 days after completion of study treatment ]
Locations (26)
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