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Epcoritamab in Combination With R-CHOP for Patients With Aggressive Non-Hodgkin Lymphoma

7 maggio 2026 aggiornato da: Mwanasha Merrill, MD

Epcoritamab in Combination With R-CHOP Debulking in Newly Diagnosed Patients With Aggressive Non-Hodgkin Lymphoma

A Phase II, open-label, two-arm, multicenter study evaluating the combination of epcoritamab with R-CHOP chemotherapy in patients with newly diagnosed, aggressive B-cell non-Hodgkin lymphoma.

Panoramica dello studio

Descrizione dettagliata

PRIMARY OBJECTIVES:

I. To evaluate the incidence and severity of all grade CRS cytokine release syndrome (CRS) in arm A and arm B.

SECONDARY OBJECTIVES:

I. To determine the safety and tolerability of the combination of epcoritamab and rituximab, cyclophosphamide, hydroxydaunorubicin, oncovin, prednisolone (R-CHOP) in both arms and individually.

II. The anti-tumor activity of epcoritamab + R-CHOP. III. To evaluate duration of response (DOR), progression-free survival (PFS), and overall survival (OS).

EXPLORATORY OBJECTIVES:

I. To evaluate changes in serum cytokine levels with epcoritamab treatment and explore their association with the incidence and severity of CRS.

II. To characterize peripheral T-cell subsets and activation states and explore phenotypic profiles associated with CRS.

OUTLINE:

Participants will receive epcoritamab combined with R-CHOP chemotherapy and dexamethasone. The treatment will be delivered in up to 8 cycles in an outpatient setting. participants are followed at Week 8 and every 3 months for up to one year, or until improvement or stabilization, or until new therapy begins, whichever occurs first.

Tipo di studio

Interventistico

Iscrizione (Stimato)

20

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: UCSF Hematopoietic Malignancies Clinical Trial Recruitment
  • Numero di telefono: 877-827-3222
  • Email: HDFCCC.Heme@ucsf.edu

Backup dei contatti dello studio

Luoghi di studio

    • California
      • San Francisco, California, Stati Uniti, 94143
        • University of California, San Francisco
        • Contatto:
        • Contatto:
          • UCSF Hematopoietic Malignancies Clinical Trial Recruitment
          • Numero di telefono: 877-827-3222
          • Email: HDFCCC.Heme@ucsf.edu
        • Investigatore principale:
          • Mwanasha Merrill, MD
      • San Francisco, California, Stati Uniti, 94110
        • Zuckerberg San Francisco General
        • Contatto:
          • UCSF Hematopoietic Malignancies Clinical Trial Recruitment
          • Numero di telefono: 877-827-3222
          • Email: HDFCCC.Heme@ucsf.edu
        • Contatto:
          • Clinical Trial Recruitment
          • Numero di telefono: cancertrials@ucsf.edu
        • Investigatore principale:
          • Mwanasha Merrill, MD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Participants must have confirmed CD20-positive aggressive B-cell lymphoma, including de novo or transformed diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS); high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangement; primary mediastinal large B-cell lymphoma (PMBCL); T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL); Epstein-Barr virus-positive DLBCL, NOS; or follicular lymphoma grade 3b.
  2. Measurable disease per Lugano 2014 criteria.
  3. No prior therapy for DLBCL or FL G3B other than corticosteroids or palliative radiotherapy. Of note, a cycle of anthracycline-containing regimen (given as standard of care prior to study enrollment) is allowed, provided that patients will receive a total of six cycles of chemotherapy as part of their treatment plan. Patients who received one cycle of an anthracycline-containing regimen prior to enrollment will proceed directly to Cycle 2 on study.
  4. Age ≥18 years
  5. Participants must have an International Prognostic Index (IPI) score of 2-5.
  6. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥ 60%)
  7. Demonstrates adequate organ function as defined below:

    Adequate bone marrow function:

    absolute neutrophil count platelets

    • 1.0 × 10⁹/Litre (L) (with growth factor use allowed)
    • 75 × 10⁹/L

    Exceptions:

    Patients may be enrolled despite not meeting the thresholds above if either of the following applies, provided the Absolute Neutrophil Count (ANC) is ≥0.75 × 10⁹/L:

    1. The patient has received one prior cycle of chemotherapy off study, and cytopenias at Cycle 2, Day 1 of protocol therapy are believed to be due to recent chemotherapy, provided there is evidence of marrow recovery and no other contraindications.
    2. The patient has documented bone marrow involvement by lymphoma, and cytopenias are believed to be disease-related rather than indicative of poor marrow reserve or unrelated pathology. In such cases, enrollment is permitted at the discretion of the investigator if the patient is otherwise eligible and deemed safe to proceed.

    Adequate hepatic function:

    Total bilirubin

    ≤2 × upper limit of normal (ULN) (unless due to Gilbert's)

    Aspartate aminotransferase (AST) Serum glutamic-oxaloacetic transaminase (SGOT)

    ≤3 × institutional upper limit of normal

    Alanine aminotransferase (ALT) Serum glutamic-pyruvic transaminase (SGPT)

    ≤3 × institutional upper limit of normal

    Adequate renal function:

    As assessed by estimated glomerular filtration rate (eGFR)

    Coagulation:

    Prothrombin time (PT) International Normalized Ratio (INR) and Activated partial thromboplastin time aPTT

    ≤1.5 × ULN, unless receiving anticoagulation therapy

  8. Left ventricular ejection fraction (LVEF) ≥50% by multigated acquisition (MUGA) or echocardiography at screening.
  9. Ability to understand and the willingness to sign a written informed consent document.
  10. .Human immunodeficiency virus (HIV)-infected individuals are eligible if the following criteria are met:

    1. Serum HIV viral load is < lower limit of detection (LLD) and controlled with antiretroviral therapy for at least 1 year prior to enrollment, with confirmatory testing at screening;
    2. CD4 count ≥ 200 cells/microliter (μL) at screening;
    3. Subject is receiving antiretroviral regimens in accordance with current International Acquired Immunodeficiency Syndrome (AIDS) Society guidelines;
    4. No evidence of AIDS-defining illnesses (other than lymphoma diagnosis) or active opportunistic infections;
    5. Antiretroviral therapy does not interfere with study medications.
  11. For participants with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.
  12. Individuals with a history of hepatitis C virus (HCV) infection must have been treated and cured. For individuals with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
  13. Individuals with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
  14. The effects of epcoritamab on the developing human fetus are unknown. For this reason, and because bispecific antibodies may be teratogenic, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, or abstinence). Woman with reproductive potential must agree to use adequate contraception during the trial, and for 12 months after the last administration of epcoritamab or according to the local prescribing information of the standard of care (SOC) regimens, whichever is the longest. Adequate contraception is defined as highly effective methods of contraception. Also refer to the local prescribing information for information regarding contraceptive requirements for the SOC regimens.
  15. A woman of childbearing potential must have a negative serum (beta-hCG) pregnancy test at screening and a negative urine pregnancy test before treatment administration on Day 1 of every cycle.
  16. A woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the trial and for 12 months after receiving the last dose of epcoritamab or according to the local prescribing information of the SOC regimens, whichever is the longest.
  17. A man who is sexually active with a woman of childbearing potential and has not had a vasectomy must agree to use a barrier method of birth control, eg, either condom with spermicidal foam/gel/film/cream/suppository or partner with occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository, and all men must also not donate sperm during the trial and for 12 months after receiving the last dose of epcoritamab or according to the local prescribing information of the SoC regimens, whichever is the longest.
  18. Participants must agree not to donate blood for 60 days after receiving the last dose of trial treatment.
  19. Participants must have a treating physician at University of California, San Francisco (UCSF) or Zuckerberg San Francisco General Hospital (ZSFGH), receive study treatment under the supervision of the study Principal Investigator or qualified study sub-investigators at the enrolling site, and be willing to comply with study procedures.

Exclusion Criteria:

  1. History of severe allergic or anaphylactic reactions to anti-CD20 mAb therapy or known allergy or intolerance to any component or excipient of epcoritamab.
  2. Any prior treatment with a bispecific antibody targeting CD3 and CD20.
  3. Treatment with an investigational drug within 4 weeks or 5 half-lives, whichever is longer, prior to the first dose of epcoritamab.
  4. Requiring immunosuppressive therapy for an ongoing baseline medical condition. For corticosteroids, prednisolone >10 mg daily (or equivalent) qualifies as immunosuppressive and thus be excluded for this use. Note: corticosteroids at any dose are permitted for control of lymphoma related symptoms, including during screening, and for any adverse events (AE) management during study.
  5. Vaccination with live vaccines within 28 days prior to the first dose of epcoritamab.
  6. Clinically significant cardiovascular disease, including:

    1. Myocardial infarction within 6 months prior to the first dose of epcoritamab, or unstable or uncontrolled disease/condition related to or affecting cardiac function (eg, unstable angina, congestive heart failure New York Heart Association Class III-IV), cardiac arrhythmia (NCI Common Terminology Criteria for Adverse Events (CTCAE) Version 5 Grade 3 or higher), or clinically significant electrocardiogram (ECG) abnormalities
    2. Screening 12-lead ECG showing a baseline QT Corrected for Heart Rate using Fridericia's Formula (QTcF) >470 msec
    3. Stroke within 6 months prior to first epcoritamab dose
  7. Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at trial enrolment or significant infections within 2 weeks prior to the first dose of epcoritamab.
  8. Active hepatitis B Virus (HBV) (Deoxyribonucleic Acid Polymerase Chain Reaction (DNA PCR) -positive) or hepatitis C (Ribonucleic Acid Polymerase Chain Reaction (RNA PCR) -positive infection). Subjects with evidence of prior HBV but who are PCR-negative are permitted in the trial but should receive prophylactic antiviral therapy. Subjects who received treatment for Hepatitis C Virus (HCV) that was intended to eradicate the virus may participate if hepatitis C Ribonucleic acid (RNA) levels are undetectable.
  9. Known past or current malignancy other than inclusion diagnosis, except for:

    1. Cervical carcinoma of Stage 1B or less
    2. Non-invasive basal cell or squamous cell skin carcinoma
    3. Non-invasive, superficial bladder cancer
    4. Prostate cancer with a current Prostate-Specific Antigen (PSA) level < 0.1 ng/milliliter (mL)
    5. Any curable cancer with a complete response (CR) of > 2 years duration.
  10. Neuropathy > grade 1 with the exception of neuropathy directly related to lymphoma (e.g., direct nerve compression from tumor).
  11. . Female who is pregnant, breast-feeding, or planning to become pregnant while enrolled in this trial or within 12 months after the last dose of epcoritamab; female subjects must also agree not to breastfeed during the entire trial and until 12 months after the last administration of study drug.
  12. Male who plans to father a child while enrolled in this trial or within 12 months after the last dose of epcoritamab.
  13. Contraindication to any of the individual drugs of the R-CHOP regimen.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Arm A: Treatment with Standard Dexamethasone (First 6 participants)
Participants will receive 8 cycles of rituximab, cyclophosphamide, hydroxydaunorubicin, oncovin, prednisolone (R-CHOP) chemotherapy combined with epcoritamab. A standard dose of dexamethasone is given in Cycle 2. Treatment includes six 21-day cycles: Cycle 1 consists of R-CHOP alone; Cycles 2-5 include R-CHOP on Day 1 with epcoritamab on Days 1, 8, and 15. In Cycle 2, dexamethasone is given on epcoritamab treatment days and for 3 subsequent days. In Cycle 6, both R-CHOP and epcoritamab are given on Day 1 only. This is followed by two 28-day consolidation cycles (Cycles 7-8) with epcoritamab on Day 1. Safety follow-up occurs at Week 8 and every 3 months for up to one year. Participants who discontinue due to adverse events will be followed until improvement or stabilization, or until new therapy begins, whichever occurs first.
Dato oralmente
Given orally and intravenously (IV)
Altri nomi:
  • R-CHOP-21
Given subcutaneously (SC)
Altri nomi:
  • EPKINLY
  • epcoritamab-bysp
Undergo imaging
Perform Blood work
Participants complete European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)
Undergo Imaging
Sperimentale: Arm B: Treatment with Modified Dexamethasone
Participants will receive 8 cycles of rituximab, cyclophosphamide, hydroxydaunorubicin, oncovin, prednisolone (R-CHOP) chemotherapy combined with epcoritamab. A modified dose of dexamethasone will be given in Cycle 2. Treatment includes six 21-day cycles: Cycle 1 consists of R-CHOP alone; Cycles 2-5 include R-CHOP on Day 1 with epcoritamab on Days 1, 8, and 15. In Cycle 2, dexamethasone is administered on epcoritamab treatment days and the following day. In Cycle 6, both R-CHOP and epcoritamab are given on Day 1 only. This is followed by two 28-day consolidation cycles (Cycles 7-8) with epcoritamab on Day 1. Safety follow-up occurs at Week 8 and every 3 months for up to one year. Participants who discontinue due to adverse events will be followed until improvement or stabilization, or until new therapy begins, whichever occurs first.
Dato oralmente
Given orally and intravenously (IV)
Altri nomi:
  • R-CHOP-21
Given subcutaneously (SC)
Altri nomi:
  • EPKINLY
  • epcoritamab-bysp
Undergo imaging
Perform Blood work
Participants complete European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)
Undergo Imaging

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Cytokine Release Syndrome (CRS) Rate
Lasso di tempo: Up to day 42
The cytokine release syndrome (CRS) rate is defined as the incidence of CRS of any grade during Cycle 2, graded according to the American Society for Transplantation and Cellular Therapy (ASTCT) consensus criteria. The proportion and corresponding 95% confidence interval will be reported.
Up to day 42

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Proportion of Participants with Treatment-emergent Adverse Events
Lasso di tempo: Up to 60 days after treatment
Proportion of participants with treatment-emergent adverse events, classified according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) v5.0. The proportion and 95% confidence interval will be reported.
Up to 60 days after treatment
Overall Response (OR)
Lasso di tempo: Up to 2 years
Overall response (OR) is defined as the proportion of treated participants who obtained an radiographic objective response confirmed complete response (CR) or confirmed partial response (PR) per Lugano Classification. The proportion and 95% confidence interval will be reported.
Up to 2 years
Duration of Overall Response
Lasso di tempo: Up to 2 years
Duration of overall response is defined as the time from first documentation of complete response (CR) or partial response (PR) to the first occurrence of disease progression, recurrence, or death, whichever occurs first. Patients without progression who are alive at the clinical cutoff will be censored at the date of their last disease assessment. Median, estimates and 95% confidence interval will be reported using the Kaplan-Meier method and Brookmeyer and Crowley method.
Up to 2 years
Median Progression-Free Survival (PFS)
Lasso di tempo: Up to 2 years
Progression-free survival (PFS) is the time from the first dose of treatment until disease progression or death, whichever occurs first. If neither event occurs, PFS is measured up to the last adequate disease assessment. If a patient is alive but has no tumor assessments after starting treatment, PFS is measured up to the first dose date. Median, estimates and 95% confidence interval will be reported using the Kaplan-Meier method and Brookmeyer and Crowley method.
Up to 2 years
Median Overall Survival (OS)
Lasso di tempo: Up to 2 years.
Overall survival (OS) is the time from the first dose of treatment until death from any cause. Patients who are still alive will be followed up to their last known contact date. Median, estimates and 95% confidence interval will be reported using the Kaplan-Meier method and Brookmeyer and Crowley method.
Up to 2 years.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Mwanasha Merrill, MD, University of California, San Francisco

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 luglio 2026

Completamento primario (Stimato)

31 luglio 2028

Completamento dello studio (Stimato)

31 luglio 2029

Date di iscrizione allo studio

Primo inviato

7 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

7 maggio 2026

Primo Inserito (Effettivo)

15 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 252526

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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