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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.

調査の概要

状態

まだ募集していません

介入・治療

詳細な説明

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)

研究の種類

介入

入学 (推定)

24

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Maryland
      • Bethesda、Maryland、アメリカ、20892
        • National Institutes of Health Clinical Center
        • コンタクト:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • 電話番号:TTY dial 711 800-411-1222
          • メール:ccopr@nih.gov

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~100年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

  • 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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Rate of complete remission (CR) or very good partial remission (VGPR)
時間枠: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)

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall survival (OS)
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Laura S Samples, M.D.、National Heart, Lung, and Blood Institute (NHLBI)

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月9日

一次修了 (推定)

2030年11月1日

研究の完了 (推定)

2033年11月1日

試験登録日

最初に提出

2026年10月19日

QC基準を満たした最初の提出物

2026年10月19日

最初の投稿 (実際)

2026年10月20日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年11月3日

最終確認日

2026年10月15日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

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