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出血のためのトシリズマブ-AAZG:虚血血管イベントの減少 (THRIVE)

2026年9月22日 更新者:University of Florida

繁栄:出血のためのトシリズマブ-Aazg:虚血血管イベントの減少

In this study, tocilizumab-aazg (TYENNE) will be administered to see whether tocilizumab-aazg is safe in patients with a burst brain aneurysm and if it may prevent strokes in patients with a burst brain aneurysm.

調査の概要

詳細な説明

This is a prospective single-arm, single-center, open-label Phase 1 trial of tocilizumab-aazg 6mg/kg IV infusion drip on Day 0 in patients with aneurysmal subarachnoid hemorrhage. The trial is designed to demonstrate safety and to detect a signal that tocilizumab-aazg prevents delayed cerebral ischemia in these patients.

研究の種類

介入

入学 (推定)

30

段階

  • フェーズ 1

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

研究場所

    • Florida
      • Gainesville、Florida、アメリカ、32608
        • 募集
        • University of Florida Health (UF Health)
        • 主任研究者:
          • Brian Hoh, MD
        • コンタクト:

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~89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:

  • Adult patients (aged ≥18 years) with Hunt Hess Grade 1-3, Fisher score 3 or 3 and 4, aneurysmal subarachnoid hemorrhage within 24 hours of symptom onset (ruptured aneurysm confirmed by CTA, MRA or DSA)
  • Must have external ventricular drain or lumbar drain, or plan to place an external ventricular drain or lumbar drain.
  • Female subjects of child-bearing potential must have negative pregnancy test
  • Signed informed consent from subject or legally authorized representative
  • Able and willing to comply with followup visits
  • For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraception, as defined below:

Women must remain abstinent or use non-hormonal contraceptive methods with a failure rate of 1% per year during the treatment period and for 2 months after the final dose of TYENNE. Women must refrain from donating or storing eggs during the same time period. A woman is considered to be of childbearing potential if she is postmenarcheal, has not reached a postmenopausal state (12 continuous months of amenorrhea with no identified cause other than menopause), and is not permanently infertile due to surgery (i.e., removal of ovaries, fallopian tubes, and/or uterus) or another cause as determined by the investigator (e.g., Müllerian agenesis). The definition of childbearing potential may be adapted for alignment with local guidelines or regulations.

The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception. If required per local guidelines or regulations, locally recognized acceptable methods of contraception and information about the reliability of abstinence will be described in the local Informed Consent Form.

The following are examples of adequate non-hormonal contraceptive methods: bilateral tubal ligation; male sterilization; copper intrauterine devices; male or female condom with or without spermicide; and cap, diaphragm, or sponge with spermicide.

• For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use a condom, and agreement to refrain from donating sperm, as defined below: With a female partner of childbearing potential or pregnant female partner, men must remain abstinent or use a condom during the treatment period and for 2 months after the dose of TYENNE to avoid exposing the embryo. Men must refrain from donating sperm during this same period.

The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of preventing drug exposure. If required per local guidelines or regulations, information about the reliability of abstinence will be described in the local Informed Consent Form.

Exclusion Criteria:

  • Evidence for vasospasm or DCI prior to study enrollment
  • Hemodynamically unstable pre-enrollment
  • Severe or unstable concomitant condition or disease (e.g., known significant neurological deficit, cancer, hematologic or coronary disease), or chronic condition (e.g., liver disease, kidney disease, or psychiatric disorder), that may increase the risk associated with study participation, or may interfere with the interpretation of study results
  • Subjects who have received an investigational product or participated in another interventional clinical study within 30 days prior to enrollment.
  • Known hypersensitivity or severe allergic reaction to tocilizumab and/or other biologics agents (i.e. shock, anaphylactic reactions)
  • Serious infection defined as pneumonia, sepsis/septic shock, and neutropenic fever prior to enrollment
  • Any previous treatment with IL-6 inhibitory therapy (e.g. satralizumab), alemtuzumab, etc.
  • Total body irradiation or bone marrow transplantation within 6 months prior to baseline.
  • Any previous treatment with anti-CD20, anti-CD19, eculizumab, belimumab, interferon, natalizumab, glatiramer acetate, fingolimod, teriflunomide or dimethyl fumarate within 6 months prior to baseline.
  • Any previous treatment with anti-CD4, cladribine or mitoxantrone within 2 years prior to baseline
  • Pregnant or breastfeeding, or intending to become pregnant during the study or within 2 months after TYENNE administration
  • Women of childbearing potential must have a negative serum pregnancy test result prior to initiation of study drug.
  • Any surgical procedure (except for minor surgeries) within 4 weeks prior to baseline.
  • Evidence of serious uncontrolled concomitant diseases that may preclude patient participation, such as: other nervous system disease, cardiovascular disease, hematologic/hematopoiesis disease, respiratory disease, muscular disease, endocrine disease, renal/urologic disease, digestive system disease, congenital or acquired severe immunodeficiency.
  • Known active infection (excluding fungal infections of nail beds or caries dentium) within 4 weeks prior to baseline.
  • History of diverticulitis that, in the principal investigator's opinion, may lead to increased risk of complications such as lower gastrointestinal perforation.
  • Evidence of active or untreated latent tuberculosis (TB; excluding patients receiving chemoprophylaxis for latent TB infection).
  • Evidence of active interstitial lung disease
  • Receipt of any live or live attenuated vaccine within 6 weeks prior to baseline and throughout the duration of the study.
  • History of malignancy within the last 5 years, including solid tumors, hematologic malignancies and in situ carcinoma (except basal cell and squamous cell carcinomas of the skin, or in situ carcinoma of the cervix uteri that have been completely excised and cured).
  • Laboratory exclusion criteria (at screening):
  • White blood cells (WBC) <3.0 x103/μL
  • Absolute neutrophil count (ANC) <2.0 x103/μL
  • Absolute lymphocyte count <0.5 x103/μL
  • Platelet count <100 x 103/μL
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >1.5 times the upper limit of normal (ULN).
  • Patient with known medical history at screening listed for the following must be excluded from this trial:
  • Evidence of chronic active hepatitis B (HBV)
  • Evidence of chronic active hepatitis C (HCV)
  • Positive for hepatitis C virus (HCV) antigen
  • Positive for hepatitis B surface antigen (HBsAg)
  • Known HIV infection.
  • Illicit drug or alcohol abuse within 12 months prior to screening, in the investigator's judgment
  • Poor peripheral venous access
  • Serious infection requiring oral or IV antibiotics prior to screening
  • Any serious medical condition or abnormality in clinical laboratory tests that, in the investigator's judgment, precludes the patient's safe participation in and completion of the study
  • History or presence of an abnormal ECG that is clinically significant in the investigator's opinion, including complete left bundle branch block, second- or third-degree atrioventricular heart block, or evidence of prior myocardial infarction

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:tocilizumab-aazg (TYENNE)

Participants will receive tocilizumab-aazg 6mg/kg IV infusion drip on Day 0 following subarachnoid hemorrhage and enrollment in the trial.

A single dose of tocilizumab-aazg (TYENNE) will be administered by intravenous drip.

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
Number of participants with elevation of liver transaminases
時間枠:up to 21 days

Elevation of liver transaminase (ALT, AST) is defined as >5x upper limit of normal.

up to 21 days
Number of participants with neutropenia
時間枠:up to 21 days

Neutropenia is defined as neutrophil count below 1 x 10^9/L.

up to 21 days
Number of participants with decreased platelet count
時間枠:up to 21 days

Decreased platelet count is defined as a platelet count below the lower institutional limit of normal.

up to 21 days
Frequency of observed and reported adverse events
時間枠:baseline up to 90 days following the last administration of study treatment or study discontinuation/termination, whichever is earlier

An adverse event will be defined as any unfavorable and unintended sign, symptom, or disease temporally associated with the use of an investigational medicinal product (IMP) or other protocol-imposed intervention, regardless of attribution.

baseline up to 90 days following the last administration of study treatment or study discontinuation/termination, whichever is earlier
Frequency of death
時間枠:baseline up to 90 days following the last administration of study treatment or study discontinuation/termination, whichever is earlier

All deaths that occur during the protocol-specified AE reporting period, regardless of attribution, will be recorded.

baseline up to 90 days following the last administration of study treatment or study discontinuation/termination, whichever is earlier

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:Brian Hoh, MD、University of Florida

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3月2日

一次修了 (推定)

2028年7月30日

研究の完了 (推定)

2028年10月30日

試験登録日

最初に提出

2025年3月3日

QC基準を満たした最初の提出物

2025年3月3日

最初の投稿 (実際)

2025年3月7日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月23日

QC基準を満たした最後の更新が送信されました

2026年9月22日

最終確認日

2026年9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

はい

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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