Nivolumab With or Without Ipilimumab in Treating Younger Patients With Recurrent or Refractory Solid Tumors or Sarcomas
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT02304458
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Metastatic Melanoma
- Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
- Recurrent Hodgkin Lymphoma
- Recurrent Malignant Solid Neoplasm
- Recurrent Melanoma
- Recurrent Neuroblastoma
- Recurrent Non-Hodgkin Lymphoma
- Recurrent Osteosarcoma
- Recurrent Rhabdomyosarcoma
- Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
- Refractory Hodgkin Lymphoma
- Refractory Malignant Solid Neoplasm
- Refractory Melanoma
- Refractory Neuroblastoma
- Refractory Non-Hodgkin Lymphoma
- Refractory Osteosarcoma
- Refractory Rhabdomyosarcoma
- Stage III Cutaneous Melanoma AJCC v7
- Stage IIIA Cutaneous Melanoma AJCC v7
- Stage IIIB Cutaneous Melanoma AJCC v7
- Stage IIIC Cutaneous Melanoma AJCC v7
- Stage IV Cutaneous Melanoma AJCC v6 and v7
- Unresectable Melanoma
Eligibility Criteria
- Sex
- ALL
- Age
- 12 Months - 30 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ipilimumab — BIOLOGICALGiven IV
- Laboratory Biomarker Analysis — OTHERCorrelative studies
- Nivolumab — BIOLOGICALGiven IV
- Pharmacological Study — OTHERCorrelative studies
Study Details
This phase I/II trial studies the side effects and best dose of nivolumab when given with or without ipilimumab to see how well they work in treating younger patients with solid tumors or sarcomas that have come back (recurrent) or do not respond to treatment (refractory). Immunotherapy with monoclonal antibodies, such as nivolumab and ipilimumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. It is not yet known whether nivolumab works better alone or with ipilimumab in treating patients with recurrent or refractory solid tumors or sarcomas.
Key Dates
- Start date
- Mar 30, 2015
- Status verified
- Sep 2023
- Primary completion
- Sep 30, 2021
- Completion
- Mar 31, 2023
Study Design
- Enrollment
- 140 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (nivolumab, ipilimumab)See Detailed Description
Primary Outcome Measure
Frequency of Dose Limiting Toxicities of Nivolumab as a Single Agent or in Combination With Ipilimumab [ Time Frame: 28 days ]
Locations (24)
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