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Epcoritamab as Consolidative Therapy for Waldenstr(SqrRoot)(Delta)m Macroglobulinemia (WM) Treated With a Bruton Tyrosine Kinase Inhibitor (BTKi)

Epcoritamab as Consolidative Therapy for Waldenstrom Macroglobulinemia (WM) Treated With a Bruton Tyrosine Kinase Inhibitor (BTKi)

Background:

Waldenstrom macroglobulinemia (WM) is a type of blood cancer. It causes the blood to get thicker, which slows circulation and makes it harder to carry oxygen and other substances around the body. WM is treated with drugs called Bruton tyrosine kinase inhibitors (BTKi). But WM never goes away completely, and sometimes it gets worse despite treatment.

Objective:

To test a new drug (epcoritamab) in people with WM.

Eligibility:

People aged 18 years or older who have WM. They must have been taking a BTKi for a year or more.

Design:

Participants will be screened. They will have blood and urine tests. They will have imaging scans and a test of their heart function. They may have a bone marrow biopsy: A large needle will be used to remove a sample of the soft tissue and fluids from inside the hip bone.

Epcoritamab is injected under the skin, normally on the lower belly or thigh. Participants will be treated in 28-day cycles. They will have 12 treatment cycles. During the first cycle, they will come to the clinic to get an injection once a week for 4 weeks. After that, they will get 1 injection on the first day of each cycle.

Blood tests and imaging scans will be repeated at study visits. A saliva sample will be taken for genetic testing. Participants will also continue their normal treatment with BTKi.

After their last treatment with the study drug, participants will have 5 follow-up visits in 6 months. Tests, including a bone marrow biopsy, may be repeated. Follow-up visits will continue every 6 months for 3 (Omega) years or more.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

Study Description:

This is a phase 2 study of adding epcoritamab as consolidative therapy for subjects with Waldenstrom macroglobulinemia (WM) receiving treatment with a Bruton tyrosine kinase inhibitor (BTKi), zanubrutinib or ibrutinib. Subjects will be treated with epcoritamab for twelve 28-day cycles. For cycle 1, patients will receive epcoritamab subcutaneously (SC) with step-up dosing (SUD; 0.16 mg on C1D1, 0.8 mg on C1D8, 3 mg on C1D15, 48 mg on C1D22). The first 3 subjects will start treatment with epcoritamab >=4 weeks apart and be hospitalized for 24 hours after the first full dose of 48 mg for observation. In the absence of grade >=3 cytokine release syndrome (CRS), subsequent subjects will be treated on an outpatient basis. Epcoritamab 48 mg SC will be administered every 4 weeks from cycles 2 to 12.

Subjects achieving complete remission (CR) or very good partial remission (VGPR) by serum IgM after 12 cycles of epcoritamab will be evaluated by bone marrow biopsy and aspirate 2 months after the last dose of epcoritamab, and elect to discontinue BTKi therapy if CR/VGPR is confirmed. For subjects who do not attain CR/VGPR, BTKi will continue as per standard of care.

Objectives:

Primary objective:

-Evaluate the efficacy of epcoritamab as consolidative therapy in WM treated with a BTKi

Secondary objectives:

  • Evaluate the safety of epcoritamab as consolidative therapy in WM treated with a BTKi
  • Evaluate other parameters of efficacy of epcoritamab as consolidative therapy in WM treated with a BTKi

Endpoints:

Primary Endpoint:

-Rate of CR/VGPR after 12 cycles of epcoritamab in WM treated with a BTKi

Secondary Endpoint:

  • Rate of cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and IgM flare
  • Incidence and severity of treatment-emergent adverse events (TEAEs)
  • Progression-free survival (PFS)
  • Duration of response after BTKi discontinuation
  • Overall survival (OS)

Tipo di studio

Interventistico

Iscrizione (Stimato)

24

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

Backup dei contatti dello studio

Luoghi di studio

    • Maryland
      • Bethesda, Maryland, Stati Uniti, 20892
        • National Institutes of Health Clinical Center
        • Contatto:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • Numero di telefono: TTY dial 711 800-411-1222
          • Email: ccopr@nih.gov

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

Da 18 anni a 100 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

  • INCLUSION CRITERIA:

Patients must meet the following entry criteria to be eligible to participate in the study:

  1. Age >=18 years

  2. Ability to comprehend the investigational nature of the study and provide informed consent

  3. Diagnosis of WM according to 11th International Workshop on WM (IWWM-11) (19)

    1. Presence of an IgM monoclonal protein
    2. Bone marrow involvement by lymphoplasmacytic lymphoma
  4. Presence of MYD88 L265P mutation

  5. Currently receiving a BTKi, zanubrutinib or ibrutinib, for >=12 months

  6. Able to obtain a commercial supply of BTKi

  7. Achieved partial response, minor response, or stable disease on a BTKi per IWWM-11 response criteria (19)

  8. A female participant is eligible to participate if not pregnant or breastfeeding, and >=1 of the following conditions applies:

    Is not a woman of childbearing potential (WOCBP)

    OR

    Is a WOCBP and

    • Uses a contraceptive method
    • Has a negative highly sensitive serum pregnancy test within 7 days before the first dose of study intervention.
  9. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 within 7 days prior to the first dose of study intervention.

  10. The ability to swallow and retain oral medication.

  11. Participants who are HBsAg positive are eligible if they have received HBV antiviral therapy for >=4 weeks and have undetectable HBV viral load prior to study entry.

    Note: Participants should remain on anti-viral therapy throughout study intervention and for at least 12 months following discontinuation of epcoritamab. Hepatitis B screening tests should include HBsAg and anti-HBV.

  12. Participants who received treatment for HCV that was intended to eradicate the virus are eligible if hepatitis C RNA levels are undetectable.

  13. COVID 19 eligibility criteria:

    Subject has no known active severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. If a subject has signs/symptoms suggestive of SARS-CoV-2 infection or have had recent known exposure to someone with SARS-CoV-2 infection, the subject must have a negative molecular (e.g., PCR) test, or 2 negative antigen test results at least 24 hours apart, to rule out SARS-CoV-2 infection.

    Subjects who do not meet SARS-CoV-2 infection eligibility criteria must be screen failed and may only rescreen after they meet the following SARS-CoV-2 infection viral clearance criteria:

    • No signs/symptoms suggestive of active SARS-CoV-2 infection
    • Negative molecular (e.g., PCR) result or 2 negative antigen test results at least 24 hours apart
  14. Adequate organ function as defined below.

**Adequate Organ Function Laboratory Values**

System

Laboratory Value

Hematological

Absolute neutrophil count (ANC)

>=1000/microL (a)

Platelets

>=75000/microL or >=50000/microLin the presence of bone marrow involvement or splenomegaly (a)

Hemoglobin

>=8 g/dL (a)

Renal

Creatinine

<=1.5 x ULN or eGFR >=30 mL/min

Hepatic

Total bilirubin

<=1.5 x ULN unless due to Gilbert's syndrome or controlled autoimmune hemolytic anemia (not requiring immunosuppressive other than <=20 mg of prednisolone daily)

AST and ALT

<=3 ULN

Coagulation

PT

aPTT

<=1.5 x ULN unless participant is receiving anticoagulant therapy

eGFR=estimated glomerular filtration rate; ALT =alanine aminotransferase; AST =aspartate aminotransferase; ULN=upper limit of normal; INR=international normalized ratio; PT=prothrombin time; aPTT=activated partial thromboplastin time

  1. Growth factor and/or transfusion support is allowed to meet this requirement at Screening only if directly attributable to WM infiltration of the bone marrow, proven by bone marrow biopsy

    EXCLUSION CRITERIA:

    An individual who meets any of the following criteria will be excluded from participation in this study:

    1. Active CNS involvement, including Bing-Neel syndrome

    2. Active HBV/HCV infection.

    3. Infection with HIV-1 or HIV-2. Exception: patients with well-controlled HIV (e.g., CD4 >350/mm^3 and undetectable viral load) are eligible.

    4. Gastrointestinal dysfunction that may affect drug absorption (e.g., gastric bypass surgery, gastrectomy).

    5. Ongoing active bacterial, viral, fungal, mycobacterial, parasitic, or other infection requiring systemic treatment (excluding prophylactic treatment) at the time of enrollment or within the previous 2 weeks prior to the first dose of epcoritamab, including COVID-19 infection. Note that a past COVID-19 infection may be a risk factor, but if resolved and the subject is vaccinated, it may be allowable to enroll the Subject.

    6. Stroke or intracranial hemorrhage within 6 months of screening

    7. Hypertensive urgency or emergency

    8. Active, clinically significant cardiovascular disease including:

    9. Uncontrolled or symptomatic arrhythmias

    10. Class 3 or 4 congestive heart failure as defined by New York Heart Association Functional Classification

      • Association and/or known decreased ejection fraction <45%
    11. Myocardial infarction, unstable angina or acute coronary syndrome within 6 months of screening.

    12. History of Mobitz II second-degree or third-degree heart block without a permanent pacemaker in place.

    13. QTcF >450 msecs based on Fridericia's formula

      Note: QTcF value may be calculated as the numerical average of up to 3 separate readings for eligibility).

    14. Known allergy/sensitivity to epcoritamab

    15. History of severe bleeding disorder defined as an ongoing congenital or acquired condition that leads to an increased likelihood of bleeding (i.e., von Willebrand's disease or hemophilia).

    16. History of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 2 years.

      Note: The time requirement does not apply to participants who underwent successful definitive resection of basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ, excluding carcinoma in situ of the bladder.

    17. Currently being treated with the following drugs:

      • CYP3A strong inducers
      • CYP3A strong inhibitors

      Note: A washout period of at least 5 times the half-life after the last dose of any of the above treatments is required for a participant to be eligible for study enrollment.

    18. Has received prior systemic anti-WM therapy besides a BTKi within 3 half-lives or 4 weeks (if prior therapy was a monoclonal antibody) of start of epcoritamab.

    19. Has received prior radiotherapy within 2 weeks of start of epcoritamab or radiation-related toxicities requiring corticosteroids.

      Note: Two weeks or fewer of palliative radiotherapy for non-CNS disease, with a 1-week washout, is permitted.

    20. Has received a live vaccine or live-attenuated vaccine within 28 days before the first dose of epcoritamab. Administration of killed vaccines are allowed.

    21. Patients requiring ongoing treatment with warfarin within 7 days of start of epcoritamab

    22. Patients who have received > 140 mg of prednisone for 14 days prior to first dose of epcoritamab or those requiring > 10 mg prednisone (or equivalent) daily, unless needed for disease control.

    23. Confirmed history or current autoimmune disease or other diseases resulting in permanent immunosuppression or requiring permanent immunosuppressive therapy. Low-dose (<=10 mg/day) prednisolone (or equivalent) for rheumatoid arthritis or similar conditions is allowed.

    24. Enrolled on another therapeutic clinical trial for WM at the start of epcoritamab. Concurrent enrollment on another therapeutic clinical trial or any trial designed to impact the efficacy of anti-cancer therapy is prohibited.

    25. Has not adequately recovered after 4 weeks from major surgery or has ongoing surgical complications.

      Note: Biopsy and placement of central venous access devices are not considered major surgery.

    26. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Epcoritamab

Epcoritamab will be administered as consolidative therapy in adults who have been receiving zanubrutinib or ibrutinib.

Step-up epcoritamab dosing during cycle 1, followed by 48 mg every 4 weeks for cycles 2-12

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Rate of complete remission (CR) or very good partial remission (VGPR)
Lasso di tempo: 12 cycles (approximately 12 months after treatment begins)

CR: No detectable monoclonal IgM, normal bone marrow morphology with no lymphoplasmacytic lymphoma involvement, and resolution of any baseline extramedullary disease.VGPR: At least a 90% reduction in serum IgM from baseline or a serum IgM level within the normal range.

12 cycles (approximately 12 months after treatment begins)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall survival (OS)
Lasso di tempo: From the first dose of epcoritamab until death or up to 5 years after the first dose.

Time from treatment initiation to death from any cause.

From the first dose of epcoritamab until death or up to 5 years after the first dose.
Duration of response (DOR) after BTKi discontinuation
Lasso di tempo: After BTKi discontinuation until loss of response, progression, death, or initiation of subsequent therapy.

The length of time that a confirmed CR or VGPR is maintained after BTKi therapy is discontinued.

After BTKi discontinuation until loss of response, progression, death, or initiation of subsequent therapy.
Progression-free survival (PFS)
Lasso di tempo: From the first dose of epcoritamab until progression or death.

Time from treatment initiation to disease progression or death from any cause.

From the first dose of epcoritamab until progression or death.
Treatment-emergent adverse events (TEAEs)
Lasso di tempo: From the first dose of epcoritamab through 60 days after the last dose, or until new systemic anticancer therapy.

Any new or worsened unfavorable medical occurrence after study treatment begins, regardless of whether it is considered treatment-related.

From the first dose of epcoritamab through 60 days after the last dose, or until new systemic anticancer therapy.
IgM flare
Lasso di tempo: Baseline, during treatment, after treatment, and following BTKi discontinuation.

Measured through serial serum IgM.

Baseline, during treatment, after treatment, and following BTKi discontinuation.
Immune effector cell associated neurotoxicity syndrome (ICANS)
Lasso di tempo: From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.

ICANs will be assessed using the 10-point ICE tool.

From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.
Cytokine release syndrome (CRS)
Lasso di tempo: From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.

CRS will be graded using the ASTCT CRS criteria.

From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.

Collaboratori e investigatori

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

Investigatori

  • Investigatore principale: Laura S Samples, M.D., National Heart, Lung, and Blood Institute (NHLBI)

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

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)

9 novembre 2026

Completamento primario (Stimato)

1 novembre 2030

Completamento dello studio (Stimato)

1 novembre 2033

Date di iscrizione allo studio

Primo inviato

19 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

19 ottobre 2026

Primo Inserito (Effettivo)

20 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 novembre 2026

Ultimo verificato

15 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

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

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

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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