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Futibatinib With Paclitaxel and Ramucirumab for the Treatment of Locally Advanced or Unresectable Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma

2026年5月13日 更新者:Northwestern University

A Phase I/Ib Dose Escalation Trial of Futibatinib in Combination With Paclitaxel/Ramucirumab in Second Line Confirmed Locally Advanced/Unresectable Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma

This phase I trial tests the safety, side effects and best dose of futibatinib with paclitaxel and ramucirumab for the treatment of patients with gastric, gastroesophageal junction or esophageal adenocarcinoma that has spread to nearby tissue or lymph nodes (locally advanced) or that cannot be removed by surgery (unresectable). Futibatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Paclitaxel is in a class of medications called antimicrotubule agents. It stops cancer cells from growing and dividing and may kill them. Ramucirumab is a monoclonal antibody that may prevent the growth of new blood vessels that tumors need to grow. Giving futibatinib with paclitaxel and ramucirumab may be safe and tolerable in treating patients with locally advanced or unresectable gastric, gastroesophageal junction or esophageal adenocarcinoma.

調査の概要

詳細な説明

PRIMARY OBJECTIVE:

I. To determine the safety, tolerability and maximum tolerated dose (MTD) for futibatinib in combination with paclitaxel/ramucirumab in patients with confirmed locally advanced/unresectable gastric, gastroesophageal junction, or esophageal adenocarcinoma.

SECONDARY OBJECTIVES:

I. To determine the toxicity profile of futibatinib in combination with paclitaxel/ramucirumab in patients with confirmed locally advanced/unresectable gastric, gastroesophageal junction, or esophageal adenocarcinoma using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTACE) version (v) 6.

II. To evaluate the preliminary activity (overall response rate [ORR], duration of response [DoR], progression free survival [PFS], overall survival [OS]) of futibatinib in combination with paclitaxel/ramucirumab in patients with confirmed locally advanced/unresectable gastric, gastroesophageal junction, or esophageal adenocarcinoma.

EXPANSION PHASE OBJECTIVE:

I. To evaluate the activity (ORR and DoR) of futibatinib in combination with paclitaxel/ramucirumab in patients with confirmed locally advanced/unresectable gastric, gastroesophageal junction, or esophageal adenocarcinoma.

OUTLINE: This is a dose-escalation study of futibatinib in combination with fixed-dose paclitaxel and ramucirumab followed by a dose-expansion study.

Patients receive ramucirumab intravenously (IV) over 30-60 minutes on days 1 and 15 of each cycle, paclitaxel IV over 60 minutes on days 1, 8 and 15 of each cycle, and futibatinib orally (PO) once daily (QD) on days 8-28 of cycle 1 and days 1-28 of subsequent cycles. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo computed tomography (CT) or magnetic resonance imaging (MRI), and optional blood and urine sample collection throughout the study.

After completion of study treatment, patients are followed up every 3 months for 2 years.

研究の種類

介入

入学 (推定)

18

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

    • Illinois
      • Chicago、Illinois、アメリカ、60611
        • Northwestern University
        • 主任研究者:
          • Chengwei Peng, MD
        • コンタクト:
    • Ohio
      • Columbus、Ohio、アメリカ、43210
        • Ohio State University
        • 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:

  • Patients must have histologically or cytologically confirmed locally advanced/unresectable gastric, gastroesophageal junction, or esophageal adenocarcinoma that is microsatellite stable and HER2 negative. (American Joint Committee on Cancer [AJCC] staging criteria; https://pmc.ncbi.nlm.nih.gov/articles/PMC5387145/)

    • Note: Histological or cytological test reports from external laboratories outside of Northwestern University (NU) will also be accepted
  • Patients must have measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1

    • Note: Patients must have documented unresectable and/or metastatic disease on CT or MRI imaging completed prior to registration. Imaging must have been completed within 90 days prior to registration for participants with measurable disease
  • Patients must not have received more than 1 prior line of therapy in the metastatic setting.

    • Note: Patients who have received neoadjuvant or adjuvant therapy must have completed therapy a year prior to registration in this study. Exception: patients with neoadjuvant or adjuvant therapy who have progressed within 6 months
  • Patients must be age ≥ 18 years
  • Patients must exhibit an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Leukocytes (white blood cells [WBC]) ≥ 2,000/mcL
  • Absolute neutrophil count (ANC) ≥ 1500/mcL
  • Hemoglobin (Hgb) ≥ 9 g/dL (transfusions within 1 week of registration are not allowed to meet cutoff)
  • Platelets (PLT) ≥ 100,000/mcL (transfusions within 1 week of registration are not allowed to meet cutoff)
  • Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) ≤ 3 x institutional ULN (unless liver metastases are present, in which case they must be ≤ 5 x ULN)
  • Alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) ≤ 3 x institutional ULN (unless liver metastases are present, in which case they must be ≤ 5 x ULN)
  • Creatinine ≤ 1.5 x Institutional ULN or meeting creatinine clearance (CrCl) criteria below
  • Creatinine clearance per the Cockcroft-Gault formula or 24-hour urine collection) ≥ 45 mL/min
  • Phosphate < ULN
  • International normalized ratio (INR) < 1.5
  • Patient's urinary protein is ≤ 1+ on dipstick or routine urinalysis (UA) within 28 days of registration.

    • Note: Random analysis of urine protein with a normal value is sufficient. If urine dipstick or routine analysis indicated proteinuria ≥ 2+, then a 24-hour urine is to be collected and demonstrate < 1000 mg of protein in 24 hours to allow participation in the study
  • For patients with a known history of human immunodeficiency virus (HIV), infected patients on effective anti-retroviral therapy must have a viral load undetectable for 6 months prior to registration.

    • Please note: this lab is not a requirement for eligibility, however, if it has been completed previously as part of the patient's health care, it should be documented for eligibility
  • Patients with known history of chronic hepatitis B virus (HBV) infection must be on suppressive therapy with an undetectable viral load.

    • Please note: this lab is not a requirement for eligibility, however if it has been completed previously as part of the patient's health care, it should be documented for eligibility
  • Patients with a known history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with a known HCV infection who are currently on treatment are eligible if they have an undetectable HCV viral load.

    • Please note: this lab is not a requirement for eligibility, however if it has been completed previously as part of the patient's health care, it should be documented for eligibility
  • Patients with treated brain metastases must not have any evidence of progression on the follow-up brain imaging after central nervous system (CNS)-directed therapy.

    • Note: All treatment for brain metastases must have been completed at least 28 days prior to registration
  • Futibatinib and other therapeutic agents used in this trial are known to be teratogenic. For this reason, patients of child-bearing potential (POCBP) and their partners with sperm-producing reproductive capacity must agree to use adequate contraception from time of informed consent, for the duration of study participation, and for 3 months following completion of study drug therapy. Should a POCBP become pregnant or suspect they are pregnant while they or their partner are participating in this study, they should inform their treating physician immediately. Patients with sperm-producing reproductive capacity (PWSPRC) treated or enrolled on this protocol must also agree to use adequate contraception with partners of childbearing potential from time of informed consent, for the duration of study participation, and 3 months after completion of study drug administration

    • Note: A POCBP is any patient (regardless of gender, sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) with an egg-producing reproductive tract who meets the following criteria:
    • Has not undergone a hysterectomy or bilateral oophorectomy
    • Has had menses at any time in the preceding 12 consecutive months (and therefore has not been naturally postmenopausal for > 12 months)
  • POCBP must have a negative pregnancy test prior to registration on study
  • Patients must have the ability to understand and the willingness to sign a written informed consent document and comply with the study requirements
  • Patients must have the ability to swallow, retain and absorb oral medications

Exclusion Criteria:

  • Patients with adenosquamous or mixed histology disease
  • Patients who have received/are receiving other investigational agents, or anticancer/antineoplastic therapy including chemotherapy, immunotherapy, biological response modifiers, anti-neoplastic endocrine therapy or devices concurrently or within 21 days or 5 times the half-life, whichever is shorter, prior to first dose of cycle 1
  • Patients who have previously received a FGFR inhibitor.

    • Note: Agents that are multi-kinase inhibitors are allowed
  • Patients who have not recovered from adverse events due to prior anti-cancer therapy (i.e., have residual toxicities > grade 1) with the exception of alopecia, neuropathy and other non-significant adverse events per NCI CTCAE v 6.0
  • Patients who have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to paclitaxel, ramucirumab, or futibatinib
  • Patients who have major surgical procedure planned during the study or any surgery within 28 days of registration or any subcutaneous venous access device placement within 7 days prior registration
  • Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, or who have experienced arterial thromboembolic events, including but not limited to myocardial infarction, transient ischemic attack, cerebrovascular accident, or unstable angina, within 6 months prior to registration ,should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification.

    • Note: To be eligible for this trial, patients should be class 2B or better
  • History of gastrointestinal perforation and/or fistulae within 6 months prior to registration
  • History of active bleeding or significant gastrointestinal (GI) bleeding requiring intervention within 60 days prior to registration
  • History and/or current evidence of endocrine alteration of calcium-phosphorus homeostasis. History and/or current evidence of ectopic mineralization/calcification including but not limited to soft tissue, kidneys, intestine, or myocardia and lung with the exception of calcified lymph nodes and asymptomatic arterial calcification
  • Current evidence of retinal disorder/keratopathy including but not limited to bullous/band keratopathy, corneal abrasion, inflammation/ulceration, keratoconjunctivitis, etc., confirmed by ophthalmologic examination
  • Patients who have an uncontrolled intercurrent illness including, but not limited to any of the following:

    • Hypertension that is not controlled on medication(per treating physician's discretion)
    • Ongoing or active infection requiring systemic treatment
    • Symptomatic congestive heart failure
    • Unstable angina pectoris
    • Cardiac arrhythmia
    • Psychiatric illness/social situations that would limit compliance with study requirements
    • Any other illness or condition that the treating investigator feels would interfere with study compliance or would compromise the patient's safety or study endpoints
  • Patients with a prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or activity assessment of the investigational regimen (per treating physician's discretion)
  • Patients who are pregnant or nursing

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:Treatment (futibatinib, paclitaxel, ramucirumab)
Patients receive ramucirumab IV over 30-60 minutes on days 1 and 15 of each cycle, paclitaxel IV over 60 minutes on days 1, 8 and 15 of each cycle, and futibatinib PO QD on days 8-28 of cycle 1 and days 1-28 of subsequent cycles. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo CT or MRI, and optional blood and urine sample collection throughout the study.
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:
  • タキソール
  • アンザタックス
  • アソタックス
  • ブリスタキソール
  • プラクセル
  • タキソール コンツェントラット
CTスキャンを受ける
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
血液と尿のサンプル採取を受ける
他の名前:
  • 生物学的サンプルの収集
  • 採取された生体試料
  • 標本収集
  • サンプル収集
与えられた IV
他の名前:
  • LY3009806
  • LY 3009806
  • IMC-1121B
  • サイラムザ
  • 抗VEGFR-2完全ヒトモノクローナル抗体 IMC-1121B
  • モノクローナル抗体HGS-ETR2
  • IMC1121B
  • LY-3009806
与えられたPO
他の名前:
  • TAS-120
  • リトゴビ
  • TAS120
  • TAS 120

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
Maximum tolerated dose
時間枠:From cycles 1 day 8 (start of Futibatinib) to cycle 2 day 8 (cycle length = 28 days)
Defined as the highest dose that causes dose-limiting toxicities (DLTs) in < 2 of 6 subjects. Will be estimated using the Bayesian Optimal Interval algorithm based on observed DLTs. The frequency of DLTs at each dose level will be summarized using descriptive statistics, including proportions and confidence intervals.
From cycles 1 day 8 (start of Futibatinib) to cycle 2 day 8 (cycle length = 28 days)
Recommended phase 2 dose
時間枠:Up to 2 years
Up to 2 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Incidence of adverse events
時間枠:Up to 2 years
Defined as the frequency of adverse events by type, severity (grade), timing, and attribution to [study drugs, according the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0.
Up to 2 years
Objective response rate
時間枠:From treatment initiation until the response has been confirmed, the patient experiences disease progression, initiates subsequent anti-cancer therapy, or completes study participation, up to 2 years after completion of study treatment
Defined as the proportion of treated patients who experience an objective response (confirmed complete response [CR] or confirmed partial response [PR]) per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. Will be calculated with corresponding 95% confidence intervals.
From treatment initiation until the response has been confirmed, the patient experiences disease progression, initiates subsequent anti-cancer therapy, or completes study participation, up to 2 years after completion of study treatment
Duration of response (DOR)
時間枠:From the first scan showing CR or PR to disease progression or death, up to 2 years after completion of study treatment
Response is defined as confirmed complete response or confirmed partial response per RECIST 1.1; and disease progression is defined as progressive disease per RECIST 1.1. Will be summarized using the Kaplan-Meier method, with estimates of median DOR and corresponding 95% confidence intervals.
From the first scan showing CR or PR to disease progression or death, up to 2 years after completion of study treatment
Progression free survival (PFS)
時間枠:From treatment initiation and the earlier of the day of first documented disease progression or death, up to 2 years after completion of study treatment
PFS will be calculated based on the Kaplan-Meier estimates of PFS. Disease progression is defined as progressive disease per RECIST 1.1, other documented clinical or radiographical progression per physician judgement, or death due to disease.
From treatment initiation and the earlier of the day of first documented disease progression or death, up to 2 years after completion of study treatment
Overall survival (OS)
時間枠:From start of treatment and the date of death from any cause, up to 2 years after completion of study treatment
Median OS will be calculated based on the Kaplan-Meier estimates of OS.
From start of treatment and the date of death from any cause, up to 2 years after completion of study treatment

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:Chengwei Peng, MD、Northwestern University

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)

2027年9月9日

一次修了 (推定)

2030年9月9日

研究の完了 (推定)

2031年9月9日

試験登録日

最初に提出

2026年5月13日

QC基準を満たした最初の提出物

2026年5月13日

最初の投稿 (実際)

2026年5月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月18日

QC基準を満たした最後の更新が送信されました

2026年5月13日

最終確認日

2026年5月1日

詳しくは

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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

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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