← Eichor
Study identifier: NCT06918912 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Loncastuximab Tesirine in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL) or High-Grade B-Cell Lymphoma (HGBCL) Following CAR-T Therapy Failure

Condition: Diffuse Large B-Cell Lymphoma · High-grade B-cell Lymphoma (HGBCL) · B-Cell Lymphoma Treatment  ·  Sponsor: Istituto Clinico Humanitas

PhasePhase 2
Planned participants50
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate whether the drug Loncastuximab Tesirine can treat patients with relapsed or refractory Diffuse Large B-Cell Lymphoma (DLBCL) or High-Grade B-Cell Lymphoma (HGBCL) who have not responded to or have had a relapse after CAR-T therapy. The main question it aims to answer is: * Can Loncastuximab Tesirine improve the overall response rate (ORR) in patients who have failed CAR-T therapy? * What are the safety and potential side effects of Loncastuximab Tesirine in this patient group? This is a single-arm clinical trial, meaning all participants will receive the same treatment and there will be no comparison group. Researchers will focus on evaluating the effectiveness of the drug in helping patients achieve a response to treatment, and they will also assess the safety of the treatment. Participants will: * Be treated with Loncastuximab Tesirine through an intravenous (IV) infusion every 3 weeks for up to 8 cycles. * Undergo regular assessments to monitor the response to treatment, including PET-CT scans and blood tests to check for markers of the disease. * Be asked to provide informed consent before beginning the study and agree to follow the study procedures, including having biopsies performed to analyze biomarkers before starting treatment. * Be followed for up to 2 years after completing the treatment to track their progress and response. This study aims to help doctors understand if Loncastuximab Tesirine can offer a new trea…

This description comes directly from the study's public registry record.

Talk to the study team

Carmelo Carlo-Stella  ·  +39 02 8224 4577  ·  carmelo.carlostella@hunimed.eu

Always discuss trial participation with your own doctor first.

Locations (7)

Azienda Ospedaliera Nazionale Santi Antonio e Biagio e Cesare ArrigoAlessandria, ALESSANDRIA, ItalyRecruiting
Azienda Ospedaliero-Universitaria di Bologna, Policlinico di Sant'OrsolaBologna, BO, ItalyRecruiting
Azienda Sanitaria Ospedaliera Santa Croce e Carle di CuneoCuneo, Cuneo, ItalyRecruiting
Ospedale San RaffaeleMilan, MILANO, ItalyRecruiting
Istituto Nazionale dei TumoriMilan, MILANO, ItalyRecruiting
Irccs Istituto Clinico HumanitasRozzano, MILANO, ItalyRecruiting
AOU Policlinico Umberto IRoma, RO, ItalyRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06918912