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Evaluation of Safety and Efficacy of Autologous LB-DTK-CMV in Patients With Antiviral-Resistant and Refractory Cytomegalovirus Retinitis.

2026年6月25日 更新者:YoungHoon Park、LucasBio

An Exploratory Clinical Study of Autologous LB-DTK-CMV in Patients With Antiviral-Resistant and Refractory Cytomegalovirus Retinitis.

The goal of this exploratory clinical study is to evaluate the safety and efficacy of Cytomegalovirus-Specific T cells (LB-DTK-CMV) to treat patients diagnosed with antiviral-resistant and refractory cytomegalovirus retinitis. The main questions it aims to answer are:

  • What adverse events occur after the infusion of LB-DTK-CMV?
  • What is the duration of efficacy following treatment?
  • Is there a clinically significant reduction in CMV viral load in plasma and aqueous humor after the infusion?
  • Is there a clinically significant improvement in clinical symptoms after the infusion?

Participants will:

  • Receive two infusions of LB-DTK-CMV at 2x10^7cells/m^2 at two-week intervals beginning at the baseline visit (Cycle 1).
  • Take a three-week resting period following completion of Cycle 1.
  • Receive two infusions of LB-DTK-CMV at 2x10^7cells/m^2 at two-week intervals beginning three weeks after the last dose of Cycle 1 (Cycle 2).

研究概览

地位

招聘中

干预/治疗

研究类型

介入性

注册 (估计的)

5

阶段

  • 不适用

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

  • 姓名:Nayoun Kim, Ph.D.
  • 电话号码:+82 1040222340
  • 邮箱:nkim@lucasbio.com

学习地点

      • Seoul、韩国、06591
        • 招聘中
        • The Catholic University of Korea Seoul ST.MARY'S Hospital
        • 首席研究员:
          • Young Hoon Park, MD-PhD

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. Patients aged 19 years or older who have been diagnosed with CMV retinitis and have undergone hematopoietic stem cell transplantation or solid organ transplantation for the treatment of hematologic malignancies, or have received high-dose immunosuppressive therapy for the treatment of autoimmune diseases, and who meet at least one of the following criteria:

    • Patients with persistent or progressive CMV retinitis despite systemic antiviral therapy or intravitreal antiviral treatment.
    • Patients who have showed persistent CMV viremia despite systemic antiviral therapy or developed new CMV retinitis.
    • Patients with CMV UL54 or UL97 mutations associated with antiviral resistance.
    • Patients with adverse effects or toxicities limiting the administration of more than one systemic antiviral drug.
  2. Patients who are pregnant and able to reduce their steroid dosage to 0.5mg/kg/day of Prednisolone (or an equivalent dose) or less.
  3. For women of childbearing potential, those who tested negative on a pregnancy test (blood test) performed on the screening visit.
  4. Individuals who have voluntarily decided to participate in this clinical study and have provided written consent to comply with the restrictions.
  5. Individuals deemed suitable as study subjects through screening tests (vital signs, physical examination, medical and surgical history, electrocardiogram, laboratory tests, etc).

Exclusion Criteria:

  1. Individuals who have received treatment with ATG (Antithymocyte Globulin), Campath (Alemtuzumab), or other T-cell immunosuppressive monoclonal antibodies within 28 days prior to the first dose.
  2. Individuals who meet any of the following criteria at the time of screening:

    • Uncontrolled hypertension

      • Systolic BP ≥ 160 mmHg or diastolic BP ≥ 100 mmHg despite taking antihypertensive medication.
    • Uncontrolled severe diabetes: Severe diabetes is defined as follows:

      • Severe hyperglycemia with HbA1C ≥ 10.0%
      • Individuals who have been hospitalized for diabetic ketoacidosis within the past 12 weeks.
      • Individuals who have received emergency treatment or been hospitalized within the past 12 weeks for severe hypoglycemia (glucose <54 mg/dL) accompanied by seizures and loss of consciousness.
    • Other viral infections

      • Hepatitis B Virus (HBV), Hepatitis C Virus (HCV)
      • However, patients who are tested negative for HBsAg and positive for Anti-HBcAb are not subject to this exclusion criterion.
    • Tuberculosis
    • Syphilis
    • Moderate or severe liver damage

      • Aspartate aminotransferase (AST) or Alanin aminotransferase (ALT) > 5 times the upper limit of normal (ULN)
    • Chronic kidney disease

      • eGFR < 30mL/min/1.73m^2
    • Other uncontrolled infections. However, the following cases are considered controlled infections and do not meet the exclusion criteria:

      • Bacterial infection: Patients must be undergoing definitive antibiotic treatment for the infection and must have shown no signs of progression of the infection for 72 hours prior to enrollment in this clinical study.
      • Fungal infection: Patients must be receiving systemic antifungal therapy and must have shown no signs of infection progression for 1 week prior to enrollment in this clinical study.
  3. Patients who have received donor lymphocyte infusion (DLI) within 28 days prior to the scheduled first dose.
  4. Patients with active malignant tumor or uncontrolled recurrence.
  5. Patients with uncontrolled ophthalmic diseases other than CMV retinitis.
  6. Female subjects who are pregnant, breastfeeding, of childbearing potential, or not using appropriate contraceptive methods.
  7. Patients with a life expectancy of less than 24 hours at the time of the screening visit.
  8. Patients who have received an investigational product from another clinical study within 24 weeks prior to administration of the investigational product in this study.
  9. Patients deemed ineligible for participation in this clinical study by the investigator.

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:治疗
  • 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:Experimental Group (All)
LB-DTK-CMV is a CMV-specific T cell therapy product derived from a patient (autologous) and is stored frozen in a colorless, transparent freeze-dried vial until thawed into liquid before administration.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Viral Load
大体时间:From screening through 24 weeks after treatment initiation
CMV viral load testing is performed using plasma and aqueous humor samples. Viral load is measured at the screening visit and weekly for the first 4 weeks after the first dose in Cycle 1 through the resting period, followed by two measurements at 2-week intervals, then once every 4 weeks, and subsequently once every 12 weeks.
From screening through 24 weeks after treatment initiation
Clinical Symptom Assessment
大体时间:From the screening through 24 weeks after treatment initiation.
Clinical symptom assessments include visual acuity test, fundus examination, and optical coherence tomography. However, optical coherence tomography only applies to patients diagnosed with CMV retinitis involving the central retina. Fluorescein angiography (FAG) may also be performed on Visit 1 and 11 if considered necessary by the investigator.
From the screening through 24 weeks after treatment initiation.
Immunogenicity Testing
大体时间:From the screening through 24 weeks after treatment initiation.
Immunogenicity testing using IFN-γ ELISpot assay is performed to quantify CMV-specific T cells and evaluate the persistence and reconstitution of the immune response.
From the screening through 24 weeks after treatment initiation.
Adverse Events
大体时间:From the baseline visit throughout 24 weeks after treatment initiation.
The investigator must confirm the occurrence of adverse events through medical examinations during regular visits throughout the clinical study period. Adverse events shall be assessed at each visit starting from the administration of the investigational drug at the baseline visit (Visit 3).
From the baseline visit throughout 24 weeks after treatment initiation.

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。

赞助

调查人员

  • 首席研究员:Young Hoon Park, MD-PhD、Department of Ophthalmology, The Catholic University of Korea Seoul St.Mary's Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

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 (实际的)

2026年4月27日

初级完成 (估计的)

2027年8月14日

研究完成 (估计的)

2027年8月14日

研究注册日期

首次提交

2026年6月25日

首先提交符合 QC 标准的

2026年6月25日

首次发布 (实际的)

2026年7月1日

研究记录更新

最后更新发布 (实际的)

2026年7月1日

上次提交的符合 QC 标准的更新

2026年6月25日

最后验证

2026年6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)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

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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