POLA-R-CHP in the First-line Treatment of Transformed DLBCL

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-80
SponsorFudan University

About this trial

This study aims to evaluate efficacy and safety of POLA-R-CHP in the treatment of patients with transformed DLBCL.

Eligibility criteria

Qualifiers

Age 18 -80 years old;

Histologically confirmed transformed DLBCL;

ECOG 0-2;

Signed informed consent form.

Disqualifiers

Individuals who are allergic to human or mouse monoclonal antibodies, or known sensitivity or allergic reaction to murine products;

Previous organ transplantation;

Prior treatment of any condition (e.g., cancer, rheumatoid arthritis) with cytotoxic drugs within 5 years at the time of screening or prior use of any anti-CD20 antibodies;

Evidence of uncontrolled significant comorbidities that may affect the patient's compliance with the study protocol or affect the interpretation of the study results, including significant cardiovascular disease (such as New York College of Cardiology Class III or IV heart disease, myocardial infarction within the past 6 months, unstable arrhythmia, or unstable angina) or pulmonary disease (including history of obstructive pulmonary disease and bronchospasm);

Trial design

Treatments tested in this trial

  • POLA-R-CHP

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators