Condition: Non-Hodgkin Lymphoma · Cytokine Release Syndrome · Sponsor: Taylor Brooks
The goal of this clinical trial is to is to determine the safety, feasibility and efficacy of siltuximab prophylaxis of cytokine release syndrome and neurotoxicity occurring after epcoritamab subcutaneous administration for participants with large b-cell lymphoma (DLBCL) or follicular lymphoma (FL). Participants will receive siltuximab, prior to the injection of epcoritamab. Epcoritamab is administered in 28 day cycles for one year. After this injection, the physician will continue to watch participants for side effects and follow the condition for a minimum of 60 days.
This description comes directly from the study's public registry record.
Taylor Brooks, MD · 1-866-223 8100 · TaussigResearch@ccf.org
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| Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center | Cleveland, Ohio, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06447376