Diffuse Large B-cell Lymphoma Clinical Trial
Official title:
A Phase 1, Open-label, Dose-escalation Study of SGN-CD19B in Patients With Relapsed or Refractory Aggressive B-cell Non-Hodgkin Lymphoma
The study will examine the safety profile of SGN-CD19B administered as a single agent. The main purpose of the study is to estimate the highest dose that does not cause unacceptable side effects of SGN-CD19B in patients with relapsed or refractory aggressive B-cell non-Hodgkin lymphoma (NHL) subtypes of diffuse large B-cell lymphoma (DLBCL) and Grade 3 follicular lymphoma (FL3). Additionally, the pharmacokinetic profile and antitumor activity of SGN-CD19B will be assessed.
SGN-CD19B will be given to patients at increasing doses every 28 days (or on an alternative
dosing schedule of every 42 days).
Individual expansion cohorts of up to approximately 20 patients will be opened at dose levels
selected by the Safety Monitoring Committee based on the aggregate known safety and activity
data to further define the safety and antitumor activity in refractory and relapsed disease
subgroups.
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