Loncastuximab Tesirine for Large B-cell Lymphoma After CAR T-cell Therapy

This study is testing a drug called Loncastuximab Tesirine (Lonca) in people with large B-cell lymphoma (LBCL) that has come back or not responded to previous treatments, specifically after CAR T-cell therapy. The goal is to see if Lonca can help patients who have had some improvement (called "partial response" or PR) after CAR T-cell therapy to achieve a complete response. Researchers will also look at the safety of Lonca and any side effects it might cause. You may be able to join if you are 18 or older and have relapsed or refractory LBCL, primary mediastinal B-cell lymphoma, transformed indolent B-cell lymphomas, or high-grade B-cell lymphoma. The study aims to enroll 30 participants.

Study design
This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 30 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary goal of the study is to measure conversion to complete response through study completion and/or an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05464719

A Phase II Study of Loncastuximab Tesirine as Consolidation Strategy in Patients With LBCL in PR After CAR T-cell Therapy

Recruiting
PHASE2Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~30 participants
Updated 2026-07-15 on ClinicalTrials.gov
What's tested:Loncastuximab Tesirine

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Rate of conversion to complete response
Measured over through study completion and or average of 1 year
Large B-cell Lymphoma
Lymphoma
1 sites across 1 states
Texas1
  • Paolo Strati, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

Opens a ready-to-send draft in your own email app — review before sending.

  • Rate of conversion to complete responsethrough study completion and or average of 1 year