Testing the Combination of Copanlisib, Nivolumab and Ipilimumab in Patients With Advanced Cancer and Lymphoma
Part of paid clinical trials in Bethesda, Maryland.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT03502733
- Phase
- PHASE1
- Status
- Active Not Recruiting
Conditions
- Lymphoma
- Metastatic Malignant Solid Neoplasm
- Recurrent Malignant Solid Neoplasm
- Unresectable Malignant Solid Neoplasm
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Biopsy Procedure — PROCEDUREUndergo tumor biopsy
- Biospecimen Collection — PROCEDUREUndergo blood sample collection
- Computed Tomography — PROCEDUREUndergo CT scan
- Copanlisib — DRUGGiven IV
- Echocardiography Test — PROCEDUREUndergo ECHO
- Ipilimumab — BIOLOGICALGiven IV
- Magnetic Resonance Imaging — PROCEDUREUndergo MRI
- Nivolumab — BIOLOGICALGiven IV
Study Details
This phase Ib trial studies the side effects and best dose of copanlisib and nivolumab and side effects of copanlisib given together with nivolumab and ipilimumab in treating patients with solid tumors that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or lymphoma. Copanlisib stops tumors from growing by blocking proteins that are known to be important for tumor cell growth. 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. Giving copanlisib together with nivolumab or with nivolumab and ipilimumab may work better in treating patients with solid tumors or lymphoma.
Key Dates
- Start date
- Aug 14, 2018
- Status verified
- Dec 2025
- Primary completion
- Jul 1, 2026
- Completion
- Jul 1, 2026
Study Design
- Enrollment
- 64 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort I (Doublet) (copanlisib, nivolumab)Patients receive copanlisib IV over 1 hour on days 1 and 15 or days 1, 8, and 15 of each cycle and nivolumab IV over 30 minutes on day 1 or days 1 and 15 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT scan and/or MRI throughout the trial. Patients undergo blood sample collection on study and during follow-up, as well as tumor biopsy on study. Patients also undergo an ECHO during screening and as clinically indicated on study.
- Experimental: Cohort II (Triplet Safety) (copanlisib, nivolumab, ipilimumab)Patients receive copanlisib IV over 1 hour on days 1, 8, and 15 of each cycle, nivolumab IV over 30 minutes on day 1 of each cycle, and ipilimumab IV over 90 minutes on day 1 for cycles 1-4. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT scan and/or MRI throughout the trial. Patients undergo an ECHO during screening and as clinically indicated on study.
- Experimental: Cohort III (Triplet) (copanlisib, nivolumab, ipilmumab)Patients receive copanlisib IV over 1 hour on days 1, 8, and 15 of each cycle, nivolumab IV over 30 minutes on day 15 of cycle 1 and then day 1 of each subsequent cycles, and ipilimumab IV over 90 minutes on day 1 for cycles 2-5. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT scan and/or MRI throughout the trial. Patients undergo blood sample collection on study and during follow-up, as well as tumor biopsy on study. Patients also undergo an ECHO during screening and as clinically indicated on study.
Primary Outcome Measure
Recommended phase 2 dose of copanlisib and nivolumab combination [ Time Frame: Up to 28 days ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| National Cancer Institute Developmental Therapeutics Clinic | Bethesda | Maryland | 20892 | - |
| National Institutes of Health Clinical Center | Bethesda | Maryland | 20892 | - |
| M D Anderson Cancer Center | Houston | Texas | 77030 | - |
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