Study of Zevalin Versus Observation in Participants at Least 60 Years Old With Newly Diagnosed Diffuse Large B-cell Lymphoma in Positron Emission Tomography (PET)-Negative Complete Remission After Rituximab-Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) or R-CHOP-like Therapy
Part of paid clinical trials in Casa Grande, Arizona.
- Sponsor
- Spectrum Pharmaceuticals, Inc
- Study ID
- NCT01510184
- Phase
- PHASE3
- Status
- Terminated
Conditions
- Diffuse Large B-cell Lymphoma
- Follicle Center Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 60 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Zevalin — DRUGZevalin administered intravenous infusion.
- Y-90-Zevalin — DRUGY-90-Zevalin administered by intravenous infusion.
- Rituximab — DRUGRituximab administered by intravenous infusion.
- In-111 Zevalin — DRUGIn-111-Zevalin administered by intravenously.
Study Details
The purpose of this study is to evaluate the efficacy and safety of Zevalin compared with observation alone in participants who are in PET-negative complete remission after first-line R-CHOP or R-CHOP like therapy.
Key Dates
- Start date
- Apr 19, 2012
- Status verified
- Nov 2021
- Primary completion
- Oct 23, 2014
- Completion
- Oct 23, 2014
Study Design
- Enrollment
- 79 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: ZevalinParticipants received rituximab 250 milligram per meter square (mg/m\^2) by intravenous infusion on Day 1. If required by the governing regulatory agency, rituximab was to be followed 4 hours later by In-111-Zevalin 5.0 millicurie (mCi) on Day 1. And on Days 7-9: participants received rituximab 250 mg/m\^2 by intravenous infusion, followed 4 hours later by Y-90-Zevalin 0.4 millicurie/kilogram (mCi/kg) 10-minute intravenous push (0.3 mCi/kg in participants with a platelet count in 100,000/ microliter \[μL\] to 149,000/μL).
- No Intervention: ObservationParticipants who were randomized in this arm group did not receive any anti-lymphoma therapy unless they had a relapse of their disease.
Primary Outcome Measure
Overall Survival (OS) for Living Participants [ Time Frame: From randomization till death or end of study, whichever occurs first (Up to approximately 2.5 years) ]
Locations (28)
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