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NCT05737628
First-in-human Dose Escalation and Expansion Study With the SIRPα-directed Monoclonal Antibody BYON4228
Conditions: Lymphoma
Sex: All
Ages: 18 Years – N/A
Phase: PHASE1
Enrollment: 100
Sponsor: Byondis B.V.
Summary
This is the first-in-human study with BYON4228, a humanized monoclonal antibody (mAb) directed against SIRPα.
Eligibility Criteria
Inclusion Criteria:Part 1 (dose escalation): B-cell NHL expressing CD20 by immunohistochemistry (IHC) or flow cytometry, relapsed/refractory (R/R) to at least 2 prior lines of therapy or autologous CAR-T cell therapy.Part 2 (dose expansion):A. Histologically confirmed diffuse large B-cell lymphoma (DLBCL) expressing CD20 by IHC or flow cytometry, R/R to frontline therapy; or R/R to second line salvage regimens or autologous hematopoietic cell transplantation or autologous CAR-T cell therapy.B. Histologically confirmed marginal zone or follicular lymphoma (Grade 1-3a) expressing CD20 by IHC or flow cytometry, R/R to at least 2 prior lines of therapy or autologous CAR-T cell therapy.Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1;Adequate organ functionExclusion Criteria:Having been treated with CD47 or SIRPα targeting agents at any time or other anticancer therapy within 4 weeks or as defined in the protocolHistory of hypersensitivity or allergic reaction to any of the excipients of BYON4228 or rituximab which led to permanent discontinuation of the treatment;Burkitt's lymphoma;Red blood cell (RBC) transfusion dependencePatients with active graft versus host disease (GVHD) or ongoing immunosuppression for GVHD;History of autoimmune hemolytic anemia or autoimmune thrombocytopenia;History of active autoimmune disorders (including but not limited to: Crohn's disease, rheumatoid arthritis, scleroderma, systemic lupus erythematosus, Grave's disease) or other conditions that compromise or impair the immune system (except for hypogammaglobulinemia);History (within 6 months prior to start IMP) or presence of clinically significant cardiovascular disease such as unstable angina, congestive heart failure, myocardial infarction, uncontrolled hypertension, or cardiac arrhythmia requiring medication;Symptomatic brain metastases, brain metastases requiring steroids or treatment for brain metastases within 8 weeksSevere active infection or other severe uncontrolled systemic disease (e.g.
advanced renal disease, pulmonary, uncontrolled diabetes mellitus, severely immunocompromised state, or metabolic disease)
Source: ClinicalTrials.gov (NCT05737628). StuddyBuddy aggregates publicly available trial information.