About this trial
An open-label, single-arm, multi-center phase 2 study to evaluate the efficacy and safety of abexinostat, as monotherapy in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL)
Eligibility criteria
Qualifiers
Histologically confirmed diffuse large B-cell lymphoma (DLBCL);
Have received only two prior standard therapy lines for diffuse large B-cell lymphoma (DLBCL) including anti- cluster of differentiation antigen (anti-CD20) antibody and cytotoxic therapy;
Confirmed to be unresponsive to the last line of therapy, or have disease progression following the last line of therapy;
Have at least one radiologically measurable lymph node or extranodal lymphoid malignant lesion;
Disqualifiers
Have primary central nervous system (CNS) lymphoma or secondary central nervous system (CNS) infiltration, transformed lymphoma, unclassified B-cell lymphoma with features intermediate between DLBCL and classical Hodgkin's lymphoma (HL), primary effusion lymphoma, plasma lymphoma;
Toxicity not yet recovered from previous anti-tumor therapies;
Uncontrolled systemic infections or infections requiring intravenous antibiotics;
Have received steroid hormone, chemotherapy, targeted therapy, radiotherapy, antibody-based therapies, within a specified amount of time per protocol;
Trial design
Treatments tested in this trial
- abexinostat