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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).

調査の概要

状態

募集

条件

研究の種類

介入

入学 (推定)

5

段階

  • 適用できない

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

  • 名前:Nayoun Kim, Ph.D.
  • 電話番号:+82 1040222340
  • メール:nkim@lucasbio.com

研究場所

      • Seoul、韓国、06591
        • 募集
        • The Catholic University of Korea Seoul ST.MARY'S Hospital
        • 主任研究者:
          • Young Hoon Park, MD-PhD

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

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: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.

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
Viral Load
時間枠: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
時間枠: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
時間枠: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
時間枠: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.

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。

スポンサー

捜査官

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

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。

一般刊行物

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 (実際)

2026年4月27日

一次修了 (推定)

2027年8月14日

研究の完了 (推定)

2027年8月14日

試験登録日

最初に提出

2026年6月25日

QC基準を満たした最初の提出物

2026年6月25日

最初の投稿 (実際)

2026年7月1日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月1日

QC基準を満たした最後の更新が送信されました

2026年6月25日

最終確認日

2026年6月1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

いいえ

米国FDA規制機器製品の研究

いいえ

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