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Combination Therapy Using Durvalumab and Histotripsy for Treatment of Intrahepatic Cholangiocarcinoma (CODAH)

2026年8月28日 更新者:University of Wisconsin, Madison

Combination Therapy Using Durvalumab and Histotripsy for Treatment of Intrahepatic Cholangiocarcinoma (CODAH Trial)

The purpose of this research is to evaluate whether adding histotripsy to maintenance durvalumab increases immune response and to assess the safety of this combination for participants with advanced intrahepatic cholangiocarcinoma (iCCA). Histotripsy is a non-invasive, non-thermal treatment that uses focused ultrasound energy to destroy tumor tissue. 12 people will be enrolled in this study.

調査の概要

状態

まだ募集していません

詳細な説明

The primary objective of this pilot phase II study is to evaluate preliminary efficacy of increased immune system activation and safety of combined histotripsy and maintenance durvalumab therapy.

The secondary objectives are to evaluate additional efficacy signal and safety of the addition of histotripsy along with continued maintenance durvalumab therapy.

Exploratory objectives include evaluation for off-target effects on iCCA tumors not targeted for histotripsy treatment and evaluation of peripheral blood samples for assessment of circulating immune biomarkers and circulating tumor DNA (ctDNA).

研究の種類

介入

入学 (推定)

12

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

研究場所

    • Wisconsin
      • Madison、Wisconsin、アメリカ、53706
        • University of Wisconsin

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:

  • Participant diagnosed with histologically confirmed intrahepatic cholangiocarcinoma

    • Participant demonstrates disease control following 18 weeks of chemotherapy (gemcitabine and/or cisplatin) and immunotherapy (durvalumab) as part of standard of care first line regimen.

      • Participants are allowed to be on maintenance durvalumab therapy following disease control at 18 weeks prior to enrollment into the study.
    • All participants must have prior biopsy confirming diagnosis of cholangiocarcinoma.
  • Participant has iCCA tumor burden appropriate for biopsy and histotripsy treatment

    • Participant able to undergo liver biopsy of Index Tumor.

      • Index Tumor will be a predetermined non-histotripsy tumor in patients with multifocal disease, or a predetermined region of intentionally untreated tumor in patients with solitary disease.
    • Participant to have iCCA deemed targetable for histotripsy.

      • Participants with solitary tumor must have longest dimension ≥ 2.0 cm to allow for planned region of intentionally untreated Target Tumor for Index Tumor.
  • Participants' iCCA is considered unresectable or patient is a non-surgical candidate
  • Participant can undergo general anesthesia.
  • Participant has a Child-Pugh Score of A or B (up to B8).
  • Participant has an Eastern Cooperative Oncology Group Performance Status (ECOG PS) grade 0-2 at baseline screening.
  • Participant meets the following functional criteria, ≤7 days prior to the planned histotripsy procedure date

    • Liver function: Alanine transaminase (ALT) and Aspartate transaminase (AST) <2.5x upper limit of normal (ULN) and/or bilirubin <2.5 ULN.
    • Renal function: serum creatinine <2x ULN.
    • Hematologic function: Absolute neutrophil count >1,000/uL and platelet >50,000/uL, hemoglobin >8.0 g/dL.
  • Participant has an International Normalized Ratio (INR) score of <3.0, ≤7 days prior to the planned histotripsy procedure date.
  • Persons of childbearing potential must have a negative pregnancy test (serum or urine) within 7 days prior to registration.
  • Females of childbearing potential who are sexually active with a male able to father a child must be willing to abstain from heterosexual vaginal intercourse or use an effective method(s) of contraception from the time of informed consent, during the study and for up to 14 months after the last dose of study drug(s). Males able to father a child must be willing to abstain from heterosexual vaginal intercourse or to use an effective method(s) of contraception from initiation of treatment, during the study and for up to 11 months after the last dose of study drug(s).
  • Ability of the participant to understand and comply with study procedures for the entire length of the study, as determined by the enrolling physician or protocol designee.

Exclusion Criteria:

  • Participant is pregnant or planning to become pregnant or nursing (lactating) during the trial period.
  • Participant is enrolled in another investigational trial and/or is taking investigational medication or treated with an investigational device ≤30-days prior to planned histotripsy procedure date.
  • In the Investigator's opinion, the subject has co-morbid disease(s) or condition(s) that would cause undue risk and preclude safe histotripsy treatment, including but not limited to interstitial lung disease, including history of interstitial lung disease or non-infectious pneumonitis.
  • Active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment. .
  • Participant has major surgical procedure or significant traumatic injury ≤2 weeks prior to the planned treatment or not fully recovered (CTCAE grade 1 or better) from side effects/complications of such procedure or trauma.
  • Participant has not recovered to Common Terminology Criteria for Adverse Events (CTCAE) grade 1 or better from any adverse effects (exceptions for alopecia, grade 2 neuropathy, grade 2 hypothyroidism, grade 2 hypoadrenalism) related to previous anti-cancer therapy. Please refer to inclusion criteria for lab-based enrollment parameters.
  • Participant has a history of bleeding disorders (e.g. von Willebrand disease) or subject is suspected to have a bleeding disorder.
  • Participant has uncorrectable coagulopathy.
  • In the opinion of the Investigator, histotripsy is not a treatment option for the subject.
  • Participant has a concurrent condition that, in the investigator's opinion, could jeopardize the safety of the subject or compliance with the protocol.
  • Participants' tumor(s) is not targetable per discretion of radiologist.
  • Participant has a known sensitivity to contrast media and cannot be adequately pre-medicated.
  • Participants' Target Tumor(s) has/have had prior locoregional therapy (e.g. ablation, embolization, radiation).
  • History of solid organ or allogeneic bone marrow transplantation.
  • Patients with a prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen are not eligible for this trial.
  • Significant dementia or other mental condition that precludes the participant's ability to consent to the study.
  • Untreated central nervous system (CNS) metastasis. Screening of asymptomatic patients for CNS metastasis is not required for enrollment.
  • Live vaccine administration within 28 days of planned initial dose of durvalumab.

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:Participants with advanced iCCA
3 research specific visits; pre-histotripsy treatment (C1D3), 14-day post histotripsy follow-up with biopsy (C1D22), and 30-day post histotripsy treatment adverse events assessment. The remaining visits, including the histotripsy treatment and durvalumab infusions, are a part of the study protocol but are part of the patient's ongoing medical care. Participants followed until progression up to 5 years.
Histotripsy will be performed using the Edison® System (HistoSonics, Inc.), which is FDA cleared for destruction of liver tissue using non thermal focused ultrasound. Performed on Cycle 1 Day 8 (C1D8) to treat the Target Tumor.
他の名前:
  • HistoSonics Edison System
Durvalumab is an immunotherapy drug and will be administered on day 1 of each 28-day cycle as per local standards. Dosing of maintenance durvalumab is 1500mg IV per FDA labeling with administration performed over 60 minutes as per standard clinical practice.
他の名前:
  • durvalumab maintenance
Two research biopsies are planned for cycle 1 day 3 and cycle 1 day 22, before and after histotripsy.

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 Increase in Adaptive Immune System Response following histotripsy
時間枠:data collected cycle 1 day 3 (C1D3) and cycle 1 day 22 (C1D22) (up to about 30 days with allowable procedural windows)
Increased adaptive immune system response following histotripsy in addition to ongoing maintenance durvalumab therapy will be interpreted as T cell infiltration, downregulation of myelosuppressive cell types, and upregulation of IFN-γ. This will be completed on the biopsy tissue (pre histotripsy in comparison to post histotripsy).
data collected cycle 1 day 3 (C1D3) and cycle 1 day 22 (C1D22) (up to about 30 days with allowable procedural windows)
Percent of Participants Experiencing Immune-mediated Adverse Events within 30 days of histotrispy
時間枠:data collected up to day 38 (30 days post-histotripsy)
data collected up to day 38 (30 days post-histotripsy)

二次結果の測定

結果測定
メジャーの説明
時間枠
全生存期間 (OS)
時間枠:最長5年
最長5年
無増悪生存期間 (PFS)
時間枠:5年まで
5年まで
Treatment Efficacy
時間枠:data collected up to day 38 (30 days post-histotripsy)
Treatment Efficacy: defined as the lack of a nodular or mass-like area of enhancement within or along the edge of completed treated tumors assessed via MR or CT imaging at 30-days post procedure
data collected up to day 38 (30 days post-histotripsy)
Hepatic toxicity profile of immunotherapy checkpoint with histotripsy reported as Incidence of Dose Limiting Toxicities per Protocol
時間枠:data collected up to day 38 (30 days post-histotripsy)
Hepatic toxicity profile of immunotherapy checkpoint with histotripsy will be assessed using CTCAE version 5 grading and summarized here by number of events.
data collected up to day 38 (30 days post-histotripsy)

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。

協力者

捜査官

  • 主任研究者:John Swietlik, MD、UW School of Medicine and Public Health

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9月1日

一次修了 (推定)

2032年8月1日

研究の完了 (推定)

2032年8月1日

試験登録日

最初に提出

2026年7月20日

QC基準を満たした最初の提出物

2026年8月10日

最初の投稿 (実際)

2026年8月14日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月2日

QC基準を満たした最後の更新が送信されました

2026年8月28日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2026-0458
  • Protocol Version 5/8/26 (その他の識別子:UW Madison)
  • SMPH / Radiology (その他の識別子:UW Madison)

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?

はい

IPD プランの説明

We would share the following de-identified data with HistoSonics, Inc.: histotripsy data, images, diagnosis, weight, height, age, and gender. The Department of Radiology Medical Imaging Research Support (MIRS) Radius team will serve as an honest broker for the sharing of coded data and images.

Results from routine (safety) blood tests and imaging assessments will be placed in participants' EMR.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP

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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

はい

米国で製造され、米国から輸出された製品。

はい

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