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AB801 in Combination With Chemotherapy and Immunotherapy for the Treatment of Patients With Borderline Resectable, Locally Advanced or Metastatic Cholangiocarcinoma or Pancreatic Cancer

2026年8月18日 更新者:Jonsson Comprehensive Cancer Center

A Phase 1/1b Trial of AB801 in Combination With Chemotherapy and PD-1/PD-L1 Blockade in Patients With Cholangiocarcinoma or Pancreatic Adenocarcinoma

This phase I trial tests the safety, side effects, best dose and effectiveness of AB801 in combination with chemotherapy and immunotherapy in treating patients with cholangiocarcinoma or pancreatic adenocarcinoma that may be removed by surgery (borderline resectable), that has spread to nearby tissue or lymph nodes (locally advanced), or that has spread from where it first started (primary site) to other places in the body (metastatic). AB801 is a drug designed to block a protein called AXL. AXL is found on the surface of certain cancer cells and plays an important role in helping tumors grow, spread to other parts of the body, and avoid the immune system. It is thought to contribute to resistance against common cancer treatments such as chemotherapy, radiation and immunotherapy. In many cancers, including cholangiocarcinoma and pancreatic adenocarcinoma, AXL is overactive and associated with worse outcomes. AB801 inhibits AXL which may make cancer cells more sensitive to chemotherapy and allow immune cells to better recognize and attack the tumor. Chemotherapy drugs, such as gemcitabine, cisplatin, oxaliplatin, irinotecan, leucovrin and fluorouracil, work in different ways to stop the growth of cancer cells either by killing the cells, by stopping them from dividing or by stopping them from spreading. Immunotherapy with monoclonal antibodies, such as durvalumab and zimberelimab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving AB801 in combination with chemotherapy and immunotherapy may better treat patients with borderline resectable, locally advanced or metastatic cholangiocarcinoma or pancreatic adenocarcinoma.

調査の概要

詳細な説明

PRIMARY OBJECTIVE:

I. Assess safety and tolerability of ligritinib (AB801) in combination with chemotherapy and immunotherapy in patients with cholangiocarcinoma and pancreatic adenocarcinoma.

SECONDARY OBJECTIVES:

I. Objective response rate. II. Progression free survival. III. Duration of response. IV. Proportion of patients taken to curative intent surgery after neoadjuvant therapy.

EXPLORATORY OBJECTIVES:

I. To evaluate the effect on AXL expression by comparing pre-treatment core biopsies with post-therapy operative specimens or biopsies taken at time of progression.

II. To evaluate the effects of study treatment on tumor microenvironment by comparing pre-treatment core biopsies with operative specimens or biopsies taken at time of progression via multiple modalities including immunohistochemistry (IHC), cytometry by time-of-flight (CyTOF), ribonucleic acid sequencing (RNA Seq)/spatial transcriptomics.

III. To assess for changes in peripheral blood throughout treatment including but not limited to soluble AXL, immune cell populations and change in systemic cytokines.

IV. To explore changes in gene alterations via whole exome sequencing.

OUTLINE: This is a dose-escalation study of AB801 followed by a dose-expansion study. Patients are assigned to 1 of 2 cohorts.

COHORT I: Patients with cholangiocarcinoma receive AB801 orally (PO) once daily (QD), gemcitabine and cisplatin intravenously (IV) over 30 minutes on days 1 and 8 and durvalumab IV over 60 minutes on day 1 of each cycle. Cycles repeat every 21 days for 24 weeks in the absence of disease progression or unacceptable toxicity.

COHORT II: Patients with pancreatic cancer receive AB801 PO QD and zimberelimab IV over 60 minutes on day 1 of each cycle. Patients receive oxaliplatin IV over 120 minutes, leucovorin IV, and irinotecan IV on days 1 and 15 of each cycle and fluorouracil IV over 46 hours on days 1 and 15 of each cycle. Cycles repeat every 28 days for 24 weeks in the absence of disease progression or unacceptable toxicity.

All patients undergo computed tomography (CT) or magnetic resonance imaging (MRI) throughout the trial as well as tissue biopsy on trial.

After completion of study treatment, patients are followed up at 30 and 90 days and then every 3 months.

研究の種類

介入

入学 (推定)

46

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。

研究場所

    • California
      • Los Angeles、California、アメリカ、90095
        • 募集
        • UCLA / Jonsson Comprehensive Cancer Center
        • 主任研究者:
          • Lee S. Rosen, 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

  • 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:

  • Male or female ≥ 18 years of age and willing and able to provide informed consent
  • Previously untreated cytologically or histologically confirmed, at least one measurable lesion via Response Evaluation Criteria in Solid Tumors (RECIST 1.1) of cholangiocarcinoma or pancreatic adenocarcinoma meeting following criteria:

    • Cholangiocarcinoma

      • Borderline resectable/locally advanced cholangiocarcinoma: to be defined as unresectable disease on evaluation by a hepatobiliary multi-disciplinary tumor board/surgeon based on tumor size/location, vascular involvement, and absence of extrahepatic metastasis.
      • Metastatic cholangiocarcinoma: Patients with metastatic cholangiocarcinoma patient who have not received prior systemic therapy
    • Pancreatic adenocarcinoma

      • Borderline resectable pancreatic adenocarcinoma: There are multiple definitions of borderline resectable pancreatic ductal adenocarcinoma (PDAC). For the purposes of this study, borderline resectable disease will be identified per the National Comprehensive Cancer Network (NCCN) criteria. Per this definition, borderline resectable PDAC is defined as the presence of any one or more of the following on CT:

        • An interface between the tumor and superior mesenteric artery (SMA) or celiac axis (CA) measuring < 180º of the circumference of the vessel wall.
        • An interface between the tumor with the common hepatic artery without extension into the celiac axis or hepatic artery bifurcation allowing for safe and complete resection and reconstruction.
        • An interface between the primary tumor and the superior mesenteric vein or portal vein (SMV-PV) measuring ≥ 180° of the circumference of the vessel wall
        • Short-segment occlusion of the SMV-PV with normal vein above and below the level of obstruction that is amenable to resection and venous reconstruction
        • An interface between the primary tumor and the inferior vena cava (IVC)
      • Locally advanced pancreatic adenocarcinoma: Multiple guidelines defining locally advanced PDAC have been developed. For the purposes of this study, locally advanced PDAC cases will be identified per the definition developed by the NCCN. Per this definition, locally advanced PDAC is defined as presence of any one or more of the following on CT:

        • Interface between the tumor and SMA or CV measuring > 180º of the circumference of the vessel wall or solid tumor contact with the CA and aortic involvement.
        • Occlusion of the SMV-PV that is not amenable to resection and venous reconstruction
    • Metastatic pancreatic adenocarcinoma: Patients with metastatic pancreatic adenocarcinoma who have not received prior systemic therapy
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
  • Absolute neutrophil count (ANC) ≥ 1.5x10^9/L
  • Platelets ≥ 100x10^9/L
  • Hemoglobin ≥ 9 g/dL
  • Creatinine clearance (Ccr) ≥ 50 mL/min (as calculated by Modified Cockcroft-Gault formula)
  • Serum total bilirubin ≤ 2x upper limit of normal (ULN) or < 3x ULN if Gilbert's syndrome
  • Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamic-pyruvic transaminase [SGPT]) ≤ 2.5 X ULN; < 5x ULN in patients with liver metastases
  • Women with no childbearing potential because of surgery or who are at least 1 year postmenopausal (ie, 12 months post last menstrual period) or with menopause confirmed by follicle-stimulating hormone testing, OR
  • Women of childbearing potential (defined as any female who has experienced menarche and is not permanently sterile or post-menopausal) must use an effective nonhormonal method of contraception (intrauterine device or intrauterine system; condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; or vasectomized male partner if he is the sole partner of that participant) or practice true abstinence for the duration of the study and for up to 14 months after the last systemic treatment
  • Male participants must use an effective method of contraception (condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; or vasectomy) or practice true abstinence as defined throughout the study and for up to 11 months after the systemic treatment
  • Immunosuppressive doses of systemic medications, such as corticosteroids or absorbed topical corticosteroids (doses > 10 mg/day prednisone or equivalent) must be discontinued at least 2 weeks (14 days) before study treatment administration. Physiologic doses of corticosteroids (≤ 10 mg/day of prednisone or its equivalent) or short pulses of corticosteroids (≤ 3 days) may be permitted
  • Products with known potential to prolong the corrected QT (QTc) interval should be avoided when possible. When able will replace non-prolonging QTc acting drug when available and if medically necessary
  • Major surgery as defined by the Investigator must be completed at least 4 weeks before study treatment administration. Participants should have recovered from the surgical procedure prior to the first dose being administered
  • Adequate baseline tumor tissue sample for correlative studies

Exclusion Criteria:

  • Previous treatment with any of planned study drugs in cholangiocarcinoma, though patients with one cycle of gemcitabine/cisplatin/durvalumab will be considered eligible
  • Previous treatment with any of planned study drugs in pancreatic adenocarcinoma, though patients with one cycle of FOLFIRINOX will be considered eligible
  • Peripheral neuropathy > grade 2
  • Known status of HIV which is not well-controlled (CD4 < 300) at the time of study eligibility. Patients with controlled and treated HIV/hepatitis C virus (HCV) and an undetectable viral load are allowed
  • Untreated hepatitis B infection; Patient has known active hepatitis B virus (HBV) or hepatitis C virus (HCV), or human immunodeficiency virus (HIV) infection (testing is not mandatory, unless known active or known history of infection or required by local regulation):

    • Participants with resolved or treated HCV (ie, HCV antibody positive but undetectable HCV ribonucleic acid [RNA]) will not be excluded from this study
  • Underlying medical conditions that, in the Investigator's opinion, will make the administration of investigational product (IP)(s) hazardous, including but not limited to:

    • Interstitial lung disease, including history of interstitial lung disease or non-infectious pneumonitis
    • Active viral, bacterial, or fungal infections requiring parenteral treatment within 14 days of the initiation of the IP,
    • Active infection or antibiotics within 48 hours prior to study screening;
    • A condition or unresolved adverse event (AE) from a prior investigational drug that may obscure the interpretation of toxicity determination or AEs,
    • History of prior solid-organ transplantation
  • Any history of malignancy less than 5 years prior to the time of study eligibility (Patients with history of skin cancers excluding melanoma and cancers with a very low risk of recurrence i.e., low grade prostate cancer, thyroid cancer and low risk cervical cancer will be eligible for participation)
  • Serious medical comorbidities such as New York Heart Association Class III/IV cardiac disease, uncontrolled cardiac arrhythmias, myocardial infarction over the past 12 months
  • Known family history or personal history of long QTc syndrome or previous drug-induced QTc prolongation of at least grade 3 (QTc > 500 ms)
  • Screening 12-lead electrocardiogram (ECG), in triplicate, with a measurable QTc interval of > 450ms
  • Known, existing uncontrolled coagulopathy. Patients who have had a venous thromboembolic event (e.g., pulmonary embolism or deep vein thrombosis) requiring anticoagulation are eligible IF: they are appropriately anticoagulated and have not had a grade 2 or greater bleeding episode in the 3 weeks before day 1
  • Known pregnancy, nursing women or positive pregnancy test. Requirement for women of childbearing potential (WOCBP): Negative serum pregnancy test at screening and serum or urine prior to dosing on cycle 1 day 1, within 24 hours prior to the start of treatment (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]). WOCBP must also have a negative serum or urine pregnancy test every 3 weeks, within 24 hours prior to the start of treatment
  • Any condition (concurrent disease, infection, or comorbidity) that interferes with ability to participate in the study, causes undue risk, or complicates the interpretation of safety data, in the opinion of the investigator
  • History of trauma or major surgery within 28 days prior to the first dose of IP
  • Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
  • Any active or documented history of autoimmune disease, including but not limited to inflammatory bowel disease, celiac disease, Wegner syndrome, Hashimoto syndrome, systemic lupus erythematosus, scleroderma, sarcoidosis, or autoimmune hepatitis, within 3 years of the first dose of study treatment, except for the following:

    • Type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders such as vitiligo, or alopecia not requiring systemic therapy, or conditions not expected to recur in the absence of an external trigger.
    • Endocrinopathies where the participant is stable on hormone replacement therapy
    • History of Hashimoto syndrome within 3 years of the first of study treatment that resolved to hypothyroidism alone

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:非ランダム化
  • 介入モデル:並列代入
  • 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:Cohort I (AB801, gemcitabine, cisplatin, durvalumab)
Patients with cholangiocarcinoma receive AB801 PO QD, gemcitabine and cisplatin IV over 30 minutes on days 1 and 8 and durvalumab IV over 60 minutes on day 1 of each cycle. Cycles repeat every 21 days for 24 weeks in the absence of disease progression or unacceptable toxicity. Patients undergo CT or MRI throughout the trial as well as tissue biopsy on trial.
MRIを受ける
他の名前:
  • MRI
  • 磁気共鳴
  • 磁気共鳴画像スキャン
  • 医用画像、磁気共鳴 / 核磁気共鳴
  • 氏
  • MRイメージング
  • MRI スキャン
  • NMRイメージング
  • NMRI
  • 核磁気共鳴イメージング
  • 磁気共鳴画像法 (MRI)
  • sMRI
  • 磁気共鳴画像法(手順)
  • 構造MRI
与えられた IV
他の名前:
  • CDDP
  • シスジアミンジクロリド白金
  • シスマプラット
  • シスプラチナム
  • ネオプラチン
  • プラチノール
  • アビプラチン
  • ブラストレム
  • ブリプラチン
  • シス-ジアミン-ジクロロ白金
  • シス-ジアミンジクロロ 白金(II)
  • シスジアミンジクロロ白金
  • Cis-ジクロロアミン プラチナ (II)
  • シス白金ジアミンジクロリド
  • シスプラチナ
  • シスプラチナⅡ
  • シスプラチナⅡジアミンジクロリド
  • シスプラチル
  • シトプラチノ
  • シトシン
  • シスプラティナ
  • DDP
  • レーダープラチン
  • メタプラチン
  • ペイロンの塩化物
  • ペロンの塩
  • プラシス
  • プラススティル
  • プラタミン
  • プラチブラスチン
  • プラチブラスチン-S
  • プラティネックス
  • プラチノール-AQ
  • プラチノール-AQ VHA プラス
  • プラチノキサン
  • 白金
  • 白金ジアミノ二塩化物
  • プラティラン
  • プラティスチン
  • プラトシン
与えられた IV
他の名前:
  • dFdCyd
  • DFDC
  • ジフルオロデオキシシチジン
CTを受ける
他の名前:
  • CT
  • 猫
  • CATスキャン
  • コンピューター断層撮影
  • コンピュータ化されたアキシャルトモグラフィー
  • CTスキャン
  • トモグラフィー
  • コンピューター断層撮影 (手順)
  • コンピューター断層撮影 (CT) スキャン
  • 診断CATスキャン
  • 診断CATスキャンサービスタイプ
与えられた IV
他の名前:
  • インフィンジ
  • 免疫グロブリン G1、抗 (ヒト プロテイン B7-H1) (ヒト モノクローナル MEDI4736 重鎖)、ヒト モノクローナル MEDI4736 カッパ鎖とのジスルフィド、二量体
  • MEDI-4736
  • MEDI4736
  • メディ 4736
組織生検を受けます
他の名前:
  • Bx
  • BIOPSY_TYPE
  • 生検
Given PO
他の名前:
  • AB 801
  • AB-801
  • AB801
  • AXL Inhibitor AB801
実験的:Cohort II (AB801, zimberelimab, FOLFIRINOX)
Patients with pancreatic cancer receive AB801 PO QD and zimberelimab IV over 60 minutes on day 1 of each cycle. Patients receive oxaliplatin IV over 120 minutes, leucovorin IV, and irinotecan IV on days 1 and 15 of each cycle and fluorouracil IV over 46 hours on days 1 and 15 of each cycle. Cycles repeat every 28 days for 24 weeks in the absence of disease progression or unacceptable toxicity. Patients undergo CT or MRI throughout the trial as well as tissue biopsy on trial.
MRIを受ける
他の名前:
  • MRI
  • 磁気共鳴
  • 磁気共鳴画像スキャン
  • 医用画像、磁気共鳴 / 核磁気共鳴
  • 氏
  • MRイメージング
  • MRI スキャン
  • NMRイメージング
  • NMRI
  • 核磁気共鳴イメージング
  • 磁気共鳴画像法 (MRI)
  • sMRI
  • 磁気共鳴画像法(手順)
  • 構造MRI
CTを受ける
他の名前:
  • CT
  • 猫
  • CATスキャン
  • コンピューター断層撮影
  • コンピュータ化されたアキシャルトモグラフィー
  • CTスキャン
  • トモグラフィー
  • コンピューター断層撮影 (手順)
  • コンピューター断層撮影 (CT) スキャン
  • 診断CATスキャン
  • 診断CATスキャンサービスタイプ
与えられた IV
他の名前:
  • 5-フルラシル
  • フルラシル
  • 5 フルオロウラシル
  • 5 フルオロウラシルム
  • 5福
  • 5-フルオロ-2,4(1H, 3H)-ピリミジンジオン
  • 5-フルオロウラシル
  • 五府
  • 5FU
  • アキュサイト
  • カラック
  • フルオロウラシル
  • フルウラシル
  • フルブラスチン
  • フルラセジル
  • フリル
  • フルロブラスチン
  • リボフルオール
  • ロ2-9757
  • Ro-2-9757
与えられた IV
他の名前:
  • 葉酸
与えられた IV
他の名前:
  • 1-OHP
  • ダコチン
  • ダクプラット
  • エロキサチン
  • アイヘン
  • ジアミノシクロヘキサン オキサラト白金
  • JM-83
  • オキサラトプラチン
  • オキサラトプラチナム
  • RP 54780
  • RP-54780
  • SR-96669
  • SR96669
  • エルプラット
  • JM83
  • RP54780
  • SR 96669
与えられた IV
組織生検を受けます
他の名前:
  • Bx
  • BIOPSY_TYPE
  • 生検
Given PO
他の名前:
  • AB 801
  • AB-801
  • AB801
  • AXL Inhibitor AB801
Give IV
他の名前:
  • AB122
  • AB-122
  • 抗PD-1モノクローナル抗体 GLS-010
  • GLS010
  • GLS-010
  • WBP-3055
  • Sepalizumab
  • WBP 3055
  • WBP3055

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
Incidence of dose limiting toxicities
時間枠:During first cycle of the dose escalation phase (cycle length = 21 days for cohort I and 28 days for cohort II)
Overall exposure to study drug, the numbers of participants completing each cycle, and the dose intensity will be summarized using descriptive statistics. The number of participants with any dose adjustment will be presented for entire treatment period as well as for each cycle. The number of participants with dose reductions, dose delays, or dose omissions will also be summarized, as will the reasons for dose adjustments. Adverse events and serious adverse events will be reported using Common Terminology Criteria for Adverse Events version 5 terminology and severity.
During first cycle of the dose escalation phase (cycle length = 21 days for cohort I and 28 days for cohort II)

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall response rate (ORR)
時間枠:Up to 2 years
Will be defined as proportion of patients with complete response (CR) or partial response (PR) at time of data analysis. ORR and their corresponding exact 2-sided 95% confidence interval will be calculated.
Up to 2 years
Overall survival
時間枠:Up to 2 years
Will be estimated using Kaplan-Meier method.
Up to 2 years
Proportion of patients take to curative surgery
時間枠:Up to 2 years
Will be analyzed using descriptive statistics.
Up to 2 years
Duration of response
時間枠:up to 2 years
Will be summarized and plotted over time by Kaplan-Meier method. Time from the first documentation of CR or PR to the date of first documentation of disease progression or death (whichever occurs first).
up to 2 years
Progression-free survival
時間枠:up to 2 years
Will be estimated using Kaplan-Meier method. Time from first study dose date to the date of first documentation of disease progression or death (whichever comes first)
up to 2 years

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。

捜査官

  • 主任研究者:Lee S Rosen、UCLA / Jonsson Comprehensive Cancer Center

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5月29日

一次修了 (推定)

2027年6月1日

研究の完了 (推定)

2028年6月1日

試験登録日

最初に提出

2026年5月27日

QC基準を満たした最初の提出物

2026年5月27日

最初の投稿 (実際)

2026年6月2日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月20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18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

追加の関連 MeSH 用語

その他の研究ID番号

  • 25-2512
  • NCI-2026-03183 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))

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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

いいえ

米国で製造され、米国から輸出された製品。

いいえ

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