Combining Loncastuximab Tesirine and Epcoritamab in Relapsed/Refractory Diffuse Large B-cell Lymphoma (DLBCL)

Recruiting now · Phase 2

Conditions studied: Aggressive Diffuse Large B-cell Lymphoma, High-grade B-cell Lymphoma (HGBL), Follicular Lymphoma (FL) Grade 3B

In brief

This is a phase II study designed to evaluate the toxicity and efficacy of the combination of loncastuximab tesirine and epcoritamab in patients with relapsed/refractory aggressive B-cell lymphoma. Chimeric antigen receptor (CAR)-T cell naive patients who have failed first-line therapy and patients who have received CAR-T cells as second-line therapy and experienced CAR-T failure will be eligible for inclusion.

Key facts

Study ID

NCT07197307

Run by

Universität Münster

People needed

120

Starts

2025-10-31

Expected to finish

2030-04-30

Last updated by the study team

2026-07-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Disease:
• Subjects with histologically confirmed relapsed/refractory DLBCL based on pathology report (WHO 2022 criteria)
• DLBCL (de novo or transformed)
• High-grade B-cell lymphoma with MYC and BCL2 rearrangements
• High-grade B-cell lymphoma, not otherwise specified (NOS)
• Follicular lymphoma grade 3B
• Diagnostic biopsy performed at the time of relapse/progressive disease no longer than 3 months before study entry must be available, with sufficient material for central review and complimentary scientific analyses. CD20 expression (or a high likelihood of CD20 expression) based on immunohistochemistry should be documented prior enrollment into the study.
• Refractory disease is defined as no remission to the last therapy. Subjects intolerant to previous therapy are excluded. Two groups of patients are eligible:
• Progressive disease (PD) or stable disease (SD) as best response to previous therapy.
• Complete (CR) or partial response (PR) as the best response after previous therapy, with biopsy-proven relapse occurring < 6 months after end of treatment.
• Relapsed disease is defined as subjects achieving complete or partial remission to previous therapy, followed by biopsy-proven relapse ≥6 months after treatment completion.
• Subjects with refractory and early relapsed (≤12 months) disease after first line anti-CD20-/anthracycline-containing therapy are eligible. Subjects with late relapsed (>12 months) disease after first line anti-CD20-/anthracycline-containing therapy can be enrolled in the study only if deemed ineligible to high dose chemotherapy (HDCT) followed by autologous stem cell transplantation (ASCT)) or if refuse to undergo HDCT/ASCT. Subjects relapsed/refractory to second line CAR-T cell therapy are eligible.
• Subject must be 18 years or older.
• Subject must be eligible to receive and in need of treatment initiation based on symptoms and/or disease burden, as assessed by the investigator.
• Eastern Cooperative Oncology Group Performance (ECOG) status 0-2.
• Subject must have one or more measurable disease sites defined as follows:
• A positron emission tomography/computed tomography (PET/CT) scan demonstrating PET- positive lesion(s) AND
• At least one measurable nodal lesion (long axis > 1.5 cm and short axis > 1.0 cm) or ≥ one measurable extra-nodal lesion (long axis > 1.0 cm) on CT scan or MRI.
• Ability to understand and willingness to sign written informed consent. Signed informed consent must be obtained before any study specific procedure.
• Contraception:
• Women of childbearing potential and sexually active men must practice a highly effective method of birth control during and after the study, consistent with local regulations regarding the use of birth control methods for subjects participating in clinical trials. Men with female partners who are of childbearing potential must agree to use a condom when sexually active or practice total abstinence from the time of giving informed consent until at least 7 months after the patient receives his last dose of study treatment. Men must agree not to donate sperm from the time of giving informed consent until at least 7 months after the patient receives his last dose of study treatment. For female subjects, they apply for 12 months after the last dose of the study drug. A woman is considered to be of childbearing potential until becoming post-menopausal or permanently sterile. Permanent sterilization methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy. Post-menopausal status is defined as no menstrual periods for a continuous 12-month period without an alternative medical cause. A post-menopausal state can be confirmed by a high follicle-stimulating hormone (FSH) level within the postmenopausal range, especially in women not using hormonal contraception or replacement therapy. The investigator or a designated associate will provide guidance to patients on achieving highly effective contraception (with a failure rate of less than 1%), such as intrauterine devices, intrauterine hormone-releasing systems, bilateral tubal occlusion, having a vasectomized partner, or sexual abstinence. Male patients are required to use condoms unless their female partner is permanently sterile.
• Women of childbearing potential participating in the study will be required to undergo a pregnancy test using either urine or serum beta-human chorionic gonadotropin (beta-hCG) at the screening visit. A negative result is necessary for inclusion in the study.
• Adequate baseline organ function tests collected no more than 7 days before starting study treatment:
• Total bilirubin ≤ 1.5 times the upper limit of normal (ULN), except for patients with Gilbert syndrome, cholestasis due to hepatic hilum adenopathies or liver involvement, or biliary obstruction due to lymphoma, who may have a total bilirubin ≤ 3 times the ULN.
• Alanine transaminase (ALT) and aspartate aminotransferase (AST) and gamma-glutamyl transferase (GGT) ≤ 2.5 times the ULN, or ≤ 5 times the ULN for patients with liver involvement by lymphoma.

You may not qualify if…

• Patients who meet any of the following criteria at the time of screening will be excluded:
• Any prior lymphoma-directed treatment, except for first-line anti-CD20-/anthracycline-containing chemoimmunotherapy or second line CAR-T cell therapy. Particularly, patients previously treated with loncastuximab tesirine and any CD3xCD20 bispecific antibody therapy are not eligible.
• Patients with late relapse (>12 months) after first-line immunochemotherapy considered HDCT/ASCT eligible as assessed by the local investigator.
• Known central nervous system (CNS) involvement.
• Diagnosed or treated for any malignancy other than r/r DLBCL, HGBL or FL grade 3B within the last 3 years, except for adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease, non-invasive basal cell or squamous cell skin carcinoma, adequately treated carcinoma in situ without evidence of disease, localized prostate cancer, post-radical prostatectomy with non-rising prostate-specific antigen levels < 0.1 ng/mL, cervical carcinoma of stage 1B or less, non-invasive, superficial bladder cancer or any curable cancer with a CR of > 2 years duration.
• Known history of human immunodeficiency virus (HIV) or active hepatitis C virus (HCV) or active hepatitis B virus (HBV) infection or any known active systemic bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds). Patients with serologic markers of HBV immunization due to vaccination (HBsAg negative, Anti-HBc negative, and Anti-HBs positive) will be eligible. Subjects who are positive for hepatitis B core antibody, hepatitis B surface antigen, or hepatitis C antibody must have a negative polymerase chain reaction (PCR) result before enrollment. Those who are PCR positive will be excluded.
• Cytomegalovirus (CMV)-PCR positive at baseline.
• Any life-threatening illness, medical condition, or organ system dysfunction that, in the investigator's opinion, could compromise the subject's safety or interfere with the feasibility to administer study drugs including active hemophagocytic lymphohistiocytosis/macrophage activation syndrome (HLH/MAS), history of cutaneous collagenous vasculopathy and capillary leak syndrome.
• Concurrent treatment with another investigational agent or radiation therapy.
• Any psychological, cognitive, familial, or social condition that, in the investigator's opinion, compromises the patient's ability to understand the patient information, give informed consent, or comply with the study protocol.
• Participation in another clinical trial.
• Known history of hypersensitivity and/or positive serum human anti-drug antibody (ADA) against any component of the study products or of the concomitant medication or an anti-CD19 antibody.
• History of Stevens-Johnson syndrome or toxic epidermal necrolysis.
• Clinically significant third space fluid accumulation (i.e., ascites requiring drainage or pleural effusion that is either requiring drainage or associated with shortness of breath; history of pericardial effusion).
• Pregnancy or breastfeeding.
• Use of any other experimental medication within 30 days or 5 half-lives prior to the start of the study drug (Cycle 1 Day 1).
• Close affiliation with the investigational site, such as being a close relative of the investigator or dependent person (e.g., employee or student of the investigational site).
• Excluded medical conditions:
• Congestive heart failure > New York Heart Association (NYHA) class 2.
• Unstable angina (angina symptoms at rest) or new-onset angina (begun within the last 3 months).
• Uncontrolled atrial or ventricular cardiac arrhythmia.
• Left ventricular ejection fraction ≤ 45%.
• Electrocardiographic evidence of acute ischemia, coronary angioplasty, or myocardial infarction within 6 months prior to screening.
• Arterial or venous thrombotic or embolic events such as cerebrovascular accident (including transient ischemic attacks), deep vein thrombosis, or pulmonary embolism within 3 months before the start of study medication.
• Congenital long QT syndrome or a QT corrected by Fridericia's formula (QTcF) interval of > 480 ms at screening (unless secondary to pacemaker or bundle branch block).

Where it is running

• Universitaetsklinikum Ulm — Ulm, Germany (enrolling)
• Universitaetsklinikum Augsburg — Augsburg, Germany (enrolling)
• Vivantes Netzwerk fuer Gesundheit — Berlin, Germany (enrolling)
• Charite Universitaetsmedizin Berlin — Berlin, Germany (enrolling)
• HELIOS Klinikum Berlin-Buch — Berlin, Germany (enrolling)
• Evangelisches Klinikum Bethel — Bielefeld, Germany (enrolling)
• Klinikum Chemnitz — Chemnitz, Germany (enrolling)
• Universitaetsklinikum Duesseldorf — Düsseldorf, Germany (enrolling)
• Universitaetsklinikum Erlangen — Erlangen, Germany (enrolling)
• Klinikum Oldenburg — Oldenburg, Germany (enrolling)
• Medizinisches Versorgungszentrum des Bruederkrankenhauses St. Josef Paderborn — Paderborn, Germany (enrolling)
• Universitaetsklinikum Regensburg — Regensburg, Germany (enrolling)
• Universitaetsklinikum Aachen — Aachen, Germany (enrolling)
• Universitaetsklinikum Frankfurt — Frankfurt, Germany (enrolling)
• Medical Center - University Of Freiburg — Freiburg im Breisgau, Germany (enrolling)
• Universitaetsmedizin Greifswald — Greifswald, Germany (enrolling)
• Universitaetsklinikum Halle (Saale) — Halle, Germany (enrolling)
• St. Barbara-Klinik Hamm — Hamm, Germany (enrolling)
• Universitaetsklinikum Heidelberg — Heidelberg, Germany (enrolling)
• Universitaet Des Saarlandes — Homburg, Germany (enrolling)
• Universitaetsklinikum Jena — Jena, Germany (enrolling)
• Staedtisches Klinikum Karlsruhe — Karlsruhe, Germany (enrolling)
• Universitaetsklinikum Schleswig-Holstein — Kiel, Germany (enrolling)
• Universitaetsklinikum Schleswig-Holstein — Lübeck, Germany (enrolling)
• Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz — Mainz, Germany (enrolling)

Full record on ClinicalTrials.gov

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