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Emapalumab Prophylaxis of Bispecific T-Cell Engagers (BiTEs) Associated CRS and ICANS

2026年5月4日 更新者:NYU Langone Health

A Phase II Study of the Interferon Gamma Inhibitor Emapalumab for Prophylaxis of Cytokine Release Syndrome and Immune Effector Cell-Associated Neurotoxicity Syndrome in Patients With Lymphoma and Multiple Myeloma Receiving Bispecific T-Cell Engagers

The purpose of this study is to evaluate emapalumab as a prophylactic therapy in preventing cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) in patients with hematologic malignancies receiving bispecific antibodies (BsAbs) as outpatient. The primary objectives of this study are to evaluate the efficacy, safety, and feasibility of prophylaxis with the interferon gamma (IFN-У -γ) inhibitor Emapalumab in preventing CRS and/or ICANS in patients receiving bispecific antibody therapy for hematologic malignancies.

研究概览

研究类型

介入性

注册 (估计的)

60

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • New York
      • Brooklyn、New York、美国、11220
        • NYU Langone Health Perlmutter Cancer Center - Sunset Park
      • Manhattan、New York、美国、10016
        • NYU Langone Health Perlmutter Cancer Center - Manhattan
      • Mineola、New York、美国、11501
        • NYU Langone Health - Long Island

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Disease Criteria:

    1. Adult patients (≥18 years) with large B-cell lymphoma (LBCL) that is refractory to first-line chemoimmunotherapy or that relapsed after first-line chemoimmunotherapy not eligible for high-dose therapy/autologous stem cell transplantation (HDT-ASCT) or Chimeric Antigen Receptor T- cell (CAR-T) therapy, or adult patients with relapsed/refractory (R/R) LBCL after two or more lines of systemic therapy, who are planned to receive a commercially approved bispecific antibody therapy (e.g. epcoritamab, glofitamab). This includes:

      • Diffuse large B-cell lymphoma (DLBCL) not otherwise specified,
      • Primary mediastinal large B-cell lymphoma,
      • High-grade B-cell lymphoma,
      • DLBCL arising from follicular lymphoma.
    2. Adult patients with R/R multiple myeloma (MM) who have received multiple lines of therapy and are planned to receive a commercially approved bispecific antibody therapy. These prior therapies will typically include a proteasome inhibitor (e.g., bortezomib, carfilzomib), an immunomodulatory drug (e.g., lenalidomide, pomalidomide), and an anti-CD38 monoclonal antibody (e.g., daratumumab).
  2. Treatment Eligibility:

    1. At least measurable disease per Lugano Criteria (for B-cell lymphomas) or per International Myeloma Working Group (IMWG) criteria (for multiple myeloma) at the time of screening.
    2. At least 2 weeks or 5 half-lives (whichever is shorter) must have elapsed since any prior systemic therapy at the time the subject is planned for bispecific antibody therapy, except for systemic inhibitory/stimulatory immune checkpoint therapy. Steroids require only a 7-day washout.
    3. At least 3 half-lives must have elapsed from any prior systemic inhibitory/stimulatory immune checkpoint molecule therapy (e.g., ipilimumab, nivolumab, pembrolizumab, atezolizumab, OX40 agonists, 4-1BB agonists, etc.) before the planned bispecific therapy.
  3. Performance Status:

    1. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
  4. Organ Function:

    1. Adequate renal, hepatic, pulmonary, and cardiac function, defined as:
    2. Absolute neutrophil count (ANC) ≥ 1000/µL,
    3. Platelet count ≥ 50,000/µL,
    4. Hgb > 7, and standard pre-medications are allowed per standard of care guidelines
    5. Patients eligible to receive the bispecifics per institutional guidelines.
    6. Absolute lymphocyte count ≥ 100/µL
    7. Creatinine clearance (as estimated by Cockcroft Gault or CKD-EPI) ≥ 30 mL/min,
    8. Serum ALT/AST ≤ 2.5 times institutional upper limit of normal (ULN),
    9. Total bilirubin ≤ 1.5 mg/dL, except in subjects with Gilbert's syndrome,
    10. Cardiac ejection fraction ≥ 40%, no clinically significant pericardial effusion, and no clinically significant ECG findings (current status)
    11. Baseline oxygen saturation > 92% on room air.
  5. Reproductive Status:

    1. Females of childbearing potential must have a negative serum or urine pregnancy test. Females who have undergone surgical sterilization or who have been postmenopausal for at least 2 years are not considered to be of childbearing potential.
    2. Women of Childbearing Potential (WOCBP) must agree to use one highly effective method of contraception, including hormonal contraceptives (e.g. combined oral contraceptives, patch, vaginal ring, injectables, and implants); intrauterine device (IUD) or intrauterine system (IUS); vasectomy or tubal ligation; and one effective method of contraception, including male condom, female condom, cervical cap, diaphragm or contraceptive sponge or abstain from heterosexual intercourse for the duration of study participation and for six months after the last bispecific antibody dose..
    3. Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment.
  6. 6. Consent:

    1. Ability to understand and willingness to sign a written informed consent document

Exclusion Criteria:

  1. Other Malignancies:

    a. History of malignancy other than nonmelanoma skin cancer or carcinoma in situ (e.g., cervix, bladder, breast) unless disease-free for at least 2 years.

    b. History of Richter's transformation of chronic lymphocytic leukemia (CLL).

  2. Stem Cell Transplantation:

    1. Autologous stem cell transplant within 6 weeks of planned bispecific antibody therapy.
    2. History of allogeneic stem cell transplantation within 6 months of planned bispecific antibody.
  3. Infections:

    1. Presence of uncontrolled fungal, bacterial, viral, or other infections at the time of screening.
    2. Patients with uncontrolled hepatitis B or C infection. Subjects with positive Hepatitis B or C serology should be started on appropriate antiviral therapy prior to Emapalumab infusion.
    3. Patients must be negative for tuberculosis (TB). Subjects positive for latent tuberculosis prior to study must be started on or have completed with appropriate treatment prior to emapalumab infusion.
    4. Patients must be negative for active cytomegalovirus (CMV, NAT), Epstein-Barr virus (EBV, NAT), and adenovirus (NAT) by PCR testing.
  4. Central nervous system (CNS) Disorders:

    a. Evidence of active CNS disease, regardless of prior CNS history. b. History or presence of CNS disorder such as seizure disorder or cerebrovascular ischemia/hemorrhage within 6 months of enrollment.

  5. Cardiac and Pulmonary Events:

    1. History of myocardial infarction, cardiac angioplasty or stenting, unstable angina, or other clinically significant cardiac disease within 6 months of enrollment.
    2. History of symptomatic pulmonary embolism within 3 months of enrollment (ongoing anticoagulation is allowed if beyond 3 months).
  6. Autoimmune Disease:

    a. History of autoimmune disease requiring ongoing systemic immunosuppression. Steroids are allowed up to 5mg prednisone-equivalent for adrenal insufficiency.

    b. Patients anticipated to require canakinumab, Janus kinase (JAK) inhibitors, Tumor necrosis factor (TNF) inhibitors, or tocilizumab for baseline autoimmune/inflammatory disease at the time of bispecific antibody therapy initiation.

  7. Vaccination:

    1. Receipt of a Bacillus Calmette-Guérin (BCG) vaccine within 12 weeks prior to screening.
    2. Receipt of any live or attenuated live vaccine (other than BCG) within 4 weeks prior to screening.
  8. Investigational Agents:

    a. Participants receiving any other investigational agents for their condition.

  9. Pregnancy or Breastfeeding:

    a. Females who are pregnant or breastfeeding, or participants unwilling to use birth control during the study and for 6 months after bispecific therapy.

  10. Inability to Participate:

    1. In the investigator's judgment, subjects unlikely to complete all protocol required study visits or procedures, including follow-up visits, or comply with study participation requirements.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Prophylactic Emapalumab
Participants will receive the investigational IFN-У inhibitor Emapalumab prior to the intended standard bispecific antibody therapy for lymphoma and multiple myeloma.
1.0 mg/kg IV one day prior to bispecific antibody therapy

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Number of participants with cytokine release syndrome (CRS) (grades 2-5, as per ASTCT criteria) and/or immune effector cell-associated neurotoxicity syndrome (ICANS) (grades 2-5, per ASTCT criteria) within 30 days of bispecific antibody administration.
大体时间:Within 30 days of treatment
Within 30 days of treatment

次要结果测量

结果测量
措施说明
大体时间
Time to onset of first occurrence of CRS/ICANS by grades 2-5
大体时间:Within 30 days of treatment
Within 30 days of treatment
Number of participants with grade 3 or higher CRS
大体时间:Within 30 days of treatment
Within 30 days of treatment
Number of participants with grade 3 or higher ICANS
大体时间:Within 30 days of treatment
Within 30 days of treatment
Number of participants with any grade non-hematologic adverse events (AEs)
大体时间:Within 30 days of treatment
Within 30 days of treatment
Number of participants with grade hematologic AEs
大体时间:Within 30 days of treatment
Within 30 days of treatment
Number of participants hospitalized within 30 days of treatment
大体时间:Within 30 days of treatment
Within 30 days of treatment
Mean CRS grade
大体时间:Within 30 days of treatment
Cytokine release syndrome (CRS) grades range from 2-5, the higher the grade the more severe the event.
Within 30 days of treatment
Mean ICANS grade
大体时间:Within 30 days of treatment
Immune effector cell-associated neurotoxicity syndrome (ICANS) grades range from 2-5, the higher the grade the more severe the event.
Within 30 days of treatment

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Oscar B. Lahoud, MD、NYU Langone Health

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年5月11日

初级完成 (估计的)

2028年5月31日

研究完成 (估计的)

2029年5月31日

研究注册日期

首次提交

2026年4月28日

首先提交符合 QC 标准的

2026年4月28日

首次发布 (实际的)

2026年5月5日

研究记录更新

最后更新发布 (实际的)

2026年5月6日

上次提交的符合 QC 标准的更新

2026年5月4日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

The de-identified participant data from the final research dataset will be shared upon reasonable request beginning 9 to 36 months after publication or as required by a condition of awards or supporting agreements, provided the requesting investigator executes a data use agreement with NYU Langone Health. This instance of data sharing will also require separate IRB review as well as review from NYU Langone's Data Sharing Strategy Board (DSSB). Requests should be directed to: Oscar.lahoud@nyulangone.org. The protocol and statistical analysis plan will be posted on Clinicaltrials.gov only as required by federal regulation or supporting awards and agreements.

IPD 共享时间框架

Beginning 9 months and ending 36 months following article publication or as required by a condition of awards and agreements supporting the research.

IPD 共享访问标准

The investigator who proposed to use the data will be granted access upon reasonable request. Requests should be directed to Oscar.lahoud@nyulangone.org. To gain access, data requestors will need to sign a data access agreement. This instance of data sharing will also require separate IRB review as well as review from NYU Langone's DSSB.

IPD 共享支持信息类型

  • 研究方案
  • 树液

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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