Treatment Study of Denintuzumab Mafodotin (SGN-CD19A) Plus RICE Versus RICE Alone for Diffuse Large B-Cell Lymphoma
Part of paid clinical trials in Little Rock, Arkansas.
- Sponsor
- Seagen Inc.
- Study ID
- NCT02592876
- Phase
- PHASE2
- Status
- Terminated
Conditions
- Follicular Lymphoma, Grade 3b
- Lymphoma, B-cell
- Lymphoma, Follicular, Grade 3b
- Lymphoma, Large B-Cell, Diffuse
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- denintuzumab mafodotin — DRUGDenintuzumab mafodotin 3 mg/kg by intravenous (IV) infusion, every 3 weeks for up to 3 cycles.
- rituximab — DRUG375 mg/m\^2 by IV infusion, every 3 weeks for up to 3 cycles
- ifosfamide — DRUG5000 mg/m\^2 by IV infusion over a 24-hour period, every 3 weeks for up to 3 cycles
- carboplatin — DRUGAUC 5mg/mL x min by IV infusion, every 3 weeks for up to 3 cycles
- etoposide — DRUG100 mg/m\^2 per day by IV infusion for 3 days, every 3 weeks for up to 3 cycles
Study Details
The purpose of this randomized, open-label study is to evaluate the safety and efficacy of denintuzumab mafodotin plus RICE (rituximab, ifosfamide, carboplatin, and etoposide) when compared to RICE alone in the treatment of patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) or Grade 3b follicular lymphoma. Eligible patients must also be candidates for autologous stem cell transplant. Patients will be randomly assigned in a 1:1 ratio to receive 3 cycles of study treatment with either denintuzumab mafodotin + RICE or RICE alone. The study will assess whether there is a difference between the 2 groups in the side effects that are reported and the number of patients who achieve complete remission at the end of their study treatment.
Key Dates
- Start date
- Oct 31, 2015
- Status verified
- Apr 2019
- Primary completion
- Apr 20, 2018
- Completion
- Apr 20, 2018
Study Design
- Enrollment
- 81 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: 19A+RICEDenintuzumab mafodotin plus rituximab, ifosfamide, carboplatin, and etoposide
- Active Comparator: RICERituximab, ifosfamide, carboplatin, and etoposide
Primary Outcome Measure
Complete Remission Rate Per Independent Review Facility [ Time Frame: Up to 4 months ]
Locations (29)
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