Study to Evaluate Efficacy and Safety of Oral Abexinostat in Patients With Relapsed or Refractory Diffuse Large B-cell Lymphoma (DLBCL)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorXynomic Pharmaceuticals, Inc.

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

Treatment groups

170 Participants
are divided into 1 treatment group

Sponsors and collaborators