このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

BSB-2002 After Cyclophosphamide and Fludarabine for the Treatment of Relapsed or Refractory Acute Myeloid Leukemia Patients With NPM1 Mutation

2026年5月6日 更新者:City of Hope Medical Center

A Phase 1 Dose Finding Study to Evaluate the Safety of BSB-2002 in Relapsed or Refractory Acute Myeloid Leukemia (AML) Patients With NPM1 Mutation

This phase I trial studies the side effects and best dose of BSB-2002 when given after cyclophosphamide and fludarabine and tests how well it works in treating NPM1-mutated acute myeloid leukemia (AML) that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory). BSB-2002 is a type of personalized autologous T cell receptor-modified T cell therapy. T cells are infection fighting blood cells that can kill cancer cells. The T cells given in this study come from the patient and have a new gene put in them that makes them able to recognize mutated NPM1, a protein on the surface of cancer cells. These NPM1 mutated-specific T cells may help the body's immune system identify and kill NPM1-mutated AML cells. Giving chemotherapy, such as cyclophosphamide and fludarabine, before BSB-2002 helps kill cancer cells in the body and helps make room in the patient's bone marrow for new blood-forming cells (stem cells) to grow. Giving BSB-2002 after cyclophosphamide and fludarabine may be safe, tolerable, and/or effective in treating relapsed or refractory AML in patients with NPM1 mutation.

調査の概要

詳細な説明

PRIMARY OBJECTIVE:

I. Evaluate the safety of BSB-2002.

SECONDARY OBJECTIVES:

I. Cellular kinetics of BSB-2002 in peripheral blood through day 365. II. Evaluate the efficacy of BSB-2002 based on IIa. Percentage of patients with complete remission (CR; including CR with measurable residual disease negative [CRMRD-], CR, CR with incomplete hematologic recovery [CRi], CR with partial hematologic recovery [CRh]) or partial remission (PR) as determined by the investigator according to the European LeukemiaNet (ELN) criteria for AML; IIb. Overall survival; IIc. Duration of response (time from first tumor assessment at which the overall response was recorded as CR/CRi / CRi, CRh [AML]) until documented relapse, or death from any cause, whichever occurred first.

EXPLORATORY OBJECTIVES:

I. Assess molecular minimal residual disease (MRD) as measured by mutation specific next generation sequencing (NGS).

II. Evaluate inflammatory cytokines and other potential biomarkers.

OUTLINE: This is a dose-escalation study of BSB-2002 in combination with cyclophosphamide and fludarabine.

Patients undergo leukapheresis between days -45 and -21 for manufacturing of BSB-2002. Patients then receive cyclophosphamide intravenously (IV) and fludarabine IV on days -5 to -3 followed by BSB-2002 IV over 30 minutes on day 0 in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo blood sample collection as well as bone marrow aspiration and possible biopsy throughout the study. Patients also undergo echocardiography during screening.

After completion of study treatment, patients are followed up at days 4, 7, 10, 14, 21, 28, 56, 90, 180, 270, and 365 and then yearly for up to 15 years.

研究の種類

介入

入学 (推定)

19

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
      • Duarte、California、アメリカ、91010
        • City of Hope Medical Center
        • コンタクト:
        • 主任研究者:
          • Ryotaro Nakamura

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:

  • Documented informed consent of the participant

    • Note: For research participants who do not speak English, a short form consent may be used with a City of Hope (COH) certified interpreter/translator to proceed with screening, while the request for a translated full consent is processed
  • Age: ≥ 18 years
  • HLA-A*02:01
  • Eastern Cooperative Oncology Group (ECOG) ≤ 2
  • Adequate venous access for apheresis or agree to use of a central line for apheresis collection
  • AML diagnosed per ELN criteria which has been treated with at least two lines of therapy, and meet one of these 3 criteria:

    • Which is relapsed (after previously complete remission, CR, CRh or CRi), OR
    • Are refractory (failed to achieve complete remission) to the last treatment

      • Primary refractory patients should have received at least two cycles of induction treatment, OR
    • MRD positive (at least 1% leukemic blasts in blood or bone marrow) after being MRD negative following the last treatment
  • Positive for NPM1 mutation type A, D, G or H. The confirmation for NPM1 mutation must be performed by NGS within 3 months from enrollment
  • If participant has had prior hematopoietic cell transplant (HCT), all 3 of the following must be met:

    • More than 3 months from transplant at the time of enrollment
    • No clinically significant graft-versus (vs)-host disease requiring systemic treatment
    • Any non-hematological toxicity related to transplant has resolved to < grade 2 per Common Terminology Criteria for Adverse Events (CTCAE)
  • Total bilirubin ≤ 2 X upper limit of normal (ULN) (unless has Gilbert's disease or related to leukemia involving the liver) (performed within 6 weeks prior to leukapheresis unless otherwise stated)
  • Aspartate aminotransferase (AST) ≤ 3.0 x ULN (unless related to leukemia involving the liver) (performed within 6 weeks prior to leukapheresis unless otherwise stated)
  • Alanine aminotransferase (ALT) ≤ 3.0 x ULN (unless related to leukemia involving the liver) (performed within 6 weeks prior to leukapheresis unless otherwise stated)
  • Creatinine clearance of ≥ 40 mL/min per 24 hour urine test or the Cockcroft-Gault formula, or serum creatinine ≤ 1.6mg/dL and the participant is not on hemodialysis (performed within 6 weeks prior to leukapheresis unless otherwise stated)
  • No history of congestive heart failure class III or IV New York Heart Association (NYHA) OR left ventricular ejection fraction (LVEF) ≥ 45% up to 90 days before enrollment
  • If able to perform pulmonary function tests: Forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC) and diffusion capacity of the lung for carbon monoxide (DLCO) (diffusion capacity) ≥ 50% of predicted (corrected for hemoglobin)

    • Note To be performed up to 90 days before enrollment
  • If unable to perform pulmonary function tests: Oxygen (O2) saturation > 92% on room air

    • Note To be performed up to 90 days before enrollment
  • Seronegative for HIV antigen (Ag)/antibody (Ab) combo and no active hepatitis C virus (HCV) and hepatitis B virus (HBV) (surface antigen negative) (performed within 6 weeks prior to leukapheresis unless otherwise stated)

    • If seropositive for HIV, HCV or HBV, nucleic acid quantitation must be performed. Viral load must be undetectable
  • Meets other institutional and federal requirements for infectious disease titer requirements

    • Note Infectious disease testing to be performed within 28 days prior to leukapheresis
  • Women of childbearing potential (WOCBP): Negative urine or serum pregnancy test (performed within 6 weeks prior to leukapheresis unless otherwise stated)

    • If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
  • Agreement by females and males of childbearing potential to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 12 months from the date of BSB-2002 infusion

    • Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for > 1 year (women only)
  • CRITERIA TO PROCEED WITH LEUKAPHERESIS: Research participant has signed the informed consent
  • CRITERIA TO PROCEED WITH LEUKAPHERESIS: Research participant must have appropriate venous access, have a central line or be willing to undergo central or temporary line placement
  • CRITERIA TO PROCEED WITH LEUKAPHERESIS: Biochemistry laboratory results have been reviewed for clinical significance and appropriate measures taken. Hematology assessments are expected to be out of the normal range and do not need to be assessed for clinical significance
  • CRITERIA TO PROCEED WITH LEUKAPHERESIS: The last dose of systemic chemotherapy must be at least 2 weeks or 5 half-lives, whichever is shorter, before the leukapheresis procedure with the following exceptions:

    • Steroids and vincristine are allowed up to 7 days prior to leukapheresis
    • Intrathecal chemotherapy is allowed up to 3 days prior to leukapheresis
    • Hydroxyurea is allowed up to 48 hours prior to leukapheresis
    • The research participant cannot be on prednisone or equivalent doses of other corticosteroids at the time of leukapheresis. Note: Topical and inhaled corticosteroids in standard doses and physiologic replacement for subjects with adrenal insufficiency are allowed
  • CRITERIA TO PROCEED WITH LEUKAPHERESIS: The last dose of prior targeted agents, immunotherapy or radiation must be at least 2 weeks or 5 half-lives, whichever is shorter, before the leukapheresis procedure
  • CRITERIA TO PROCEED WITH LEUKAPHERESIS: If the research participant has undergone prior HCT, at least 3 months must have elapsed since receiving transplant to undergo peripheral blood mononuclear cell (PBMC) collection for BSB-2002 manufacturing
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Research participant's BSB-2002 product is received by COH
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Biochemistry laboratory results have been reviewed for clinical significance and appropriate measures taken. Hematology assessments are expected to be out of the normal range and do not need to be assessed for clinical significance
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Research participant with no active CNS leukemia
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Research participant must meet the following washout criteria:

    • Regimen: Hydroxyurea; Required washout period: Stopped prior to start of lymphodepletion
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: ECOG ≤ 2
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Women of childbearing potential (WOCBP): negative urine or serum pregnancy test within 30 days prior to the start of lymphodepletion. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Research participants of reproductive potential must agree to use and utilize an adequate method of contraception throughout treatment and for at least 12 months after BSB-2002 T cell infusion
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Not requiring supplemental oxygen or mechanical ventilation, oxygen saturation 92% or higher on room air
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Not requiring pressor support, no symptomatic cardiac arrhythmias, no acute coronary syndrome, or uncontrolled hypertension
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Calculated creatinine clearance (absolute value) of ≥ 40 mL/minute
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Total bilirubin ≤ 2 times the institutional upper limit of normal (ULN)

    • Note: In the event a participant has elevated levels of liver enzymes possibly related to underlying disease/disease progression, the participant will still be considered eligible
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: ALT ≤ 3 times the institutional ULN

    • Note: In the event a participant has elevated levels of liver enzymes possibly related to underlying disease/disease progression, the participant will still be considered eligible
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: AST ≤ 3 times the institutional ULN

    • Note: In the event a participant has elevated levels of liver enzymes possibly related to underlying disease/disease progression, the participant will still be considered eligible
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: No new neurological deficits
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: No clinical evidence of uncontrolled active infectious process
  • CRITERIA TO PROCEED WITH LYMPHODEPLETION: Participants must be cytomegalovirus (CMV) negative (by polymerase chain reaction [PCR])
  • CRITERIA TO PROCEED WITH BSB-2002 INFUSION: Biochemistry laboratory results have been reviewed for clinical significance and appropriate measures taken. Hematology assessments are expected to be out of the normal range and do not need to be assessed for clinical significance
  • CRITERIA TO PROCEED WITH BSB-2002 INFUSION: Prohibited medications have not been administered
  • CRITERIA TO PROCEED WITH BSB-2002 INFUSION: ECOG ≤ 2
  • CRITERIA TO PROCEED WITH BSB-2002 INFUSION: Absolute lymphocyte count (ALC) < 500/µL (0.5 × 10^⁹/L)

    • Discuss with sponsor if ALC target is not achieved by day -1
  • CRITERIA TO PROCEED WITH BSB-2002 INFUSION: Patient must not have any medical condition that render the patient unstable, including but not limited to untreated infection, altered mental status, unstable vital signs, worsening cardiovascular status, requiring discussion with the sponsor

Exclusion Criteria:

  • Leukemic blast count of > 20,000/µl. If the blast count can be maintained below the threshold with hydroxyurea, the patient would be eligible
  • Extramedullary only AML
  • Central nervous system (CNS) involvement refractory to intrathecal chemotherapy and/or standard cranial- spinal radiation
  • Candidates for hematopoietic cell transplant
  • Eligible to receive an approved targeted therapy
  • Treatment with other investigational agents within 5 half-lives of the planned dosing of BSB-2002 (day 0)
  • Ongoing treatment with chronic immunosuppressants (e.g., cyclosporine or systemic steroids at any dose)
  • Unstable cardiac disease as defined by one of the following:

    • Cardiac events such as myocardial infarction (MI) within the past 6 months
    • NYHA (New York Heart Association) heart failure class III-IV
    • Uncontrolled atrial fibrillation or hypertension
  • Uncontrolled bacterial, viral, or fungal infections at time of enrollment
  • Other active malignancy that requires treatment. Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
  • Females only: Pregnant or breastfeeding
  • Any other condition that would, in the Investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures or interference with study participation or data interpretation
  • Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)

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 (cyclophosphamide, fludarabine, BSB-2002)
Patients undergo leukapheresis between days -45 and -21 for manufacturing of BSB-2002. Patients then receive cyclophosphamide IV and fludarabine IV on days -5 to -3 followed by BSB-2002 IV over 30 minutes on day 0 in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo blood sample collection as well as bone marrow aspiration and possible biopsy throughout the study. Patients also undergo echocardiography during screening.
採血を受ける
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
与えられた IV
他の名前:
  • シトキサン
  • CTX
  • (-)-シクロホスファミド
  • 2H-1,3,2-オキサザホスホリン、2-[ビス(2-クロロエチル)アミノ]テトラヒドロ-、2-オキシド、一水和物
  • カルロキサン
  • シクロホスファミダ
  • シクロホスファミド
  • シクロキサール
  • クラフェン
  • CP一水和物
  • サイクロセル
  • シクロスブラスチン
  • シクロブラスチン
  • シクロホスファム
  • シクロホスファミド一水和物
  • シクロホスファミダム
  • シクロホスファン
  • シクロホスファナム
  • シクロスチン
  • サイトホスファン
  • シトホスファン
  • フォスファセロン
  • ジェノクサル
  • ジェヌサル
  • レドキシン
  • ミトキサン
  • ネオサー
  • レビミューン
  • WR-138719
  • アスタB518
  • B-518
  • B518
  • WR 138719
  • WR138719
与えられた IV
他の名前:
  • フルラドサ
白血球除去療法を受ける
他の名前:
  • 白血球除去法
  • 治療的白血球除去療法
  • 白血球吸着アフェレーシス
  • 白血球減少アフェレーシス
骨髄吸引を受ける
骨髄生検を受ける
他の名前:
  • 骨髄の生検
  • 生検、骨髄
心エコー検査を受けます
他の名前:
  • 心エコー検査
  • EC
Given BSB-2002 IV
他の名前:
  • 単剤療法
  • ドラッグ単剤療法
  • 単一のエージェント治療
  • 単一の薬物療法

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 toxicity
時間枠:From the start of the infusion on day 0 through day 28
Dose-limiting toxicity (DLT) will be assessed using the National Cancer Institute (NCI)'s Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Adverse events will be coded according to the Medical Dictionary for Regulatory Activities. Each adverse event will be counted once per patient. Separate tables and listings will present treatment-emergent adverse events (TEAEs), Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESI), and dose-limiting toxicities (DLT). Tables will include system organ class, high-level term, and severity grade. Listings will also include treatment interruption or discontinuation, dose level, relevant severity scales, relationship to study intervention, expectedness, onset day, duration day, action taken, outcome, sex, age, and race.
From the start of the infusion on day 0 through day 28
Frequency and severity of adverse events (AEs)
時間枠:Up to day +365
AEs will be graded by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) scale version (v) 5.0, cytokine release syndrome (CRS) and neurotoxicity (immune effector cell associated neurotoxicity syndrome [ICANS]) events will be graded by the American Society for Transplantation and Cellular Therapy (ASTCT) Consensus criteria scales for CRS and ICANS, respectively. Tables and listings will present AEs. Tables will include system organ class, high-level term, and severity grade. Listings will also include treatment interruption or discontinuation, dose level, relevant severity scales, relationship to study intervention, expectedness, onset day, duration day, action taken, outcome, sex, age, and race.
Up to day +365
Frequency and severity of serious AEs
時間枠:Up to day +365
AEs will be graded by NCI CTCAE scale v 5.0, CRS and neurotoxicity (ICANS-Immune Effector Cell-Associated Neurotoxicity) events will be graded by the ASTCT Consensus criteria scales for CRS and ICANS, respectively. Tables and listings will present serious AEs. Tables will include system organ class, high-level term, and severity grade. Listings will also include treatment interruption or discontinuation, dose level, relevant severity scales, relationship to study intervention, expectedness, onset day, duration day, action taken, outcome, sex, age, and race.
Up to day +365

二次結果の測定

結果測定
メジャーの説明
時間枠
Complete remission (CR)
時間枠:Up to day +365
Will assess the percentage of patients achieving CR (including CR with measurable residual disease negative, CR, CR with incomplete hematologic recovery [CRi], CR with partial hematologic recovery [CRh]) or partial remission as determined by the investigator according to the European LeukemiaNet criteria for acute myeloid leukemia. Will provide listings of patients who experience complete remission, including CR, CRi, and CRh, and partial remission.
Up to day +365
Duration of response
時間枠:From first tumor assessment at which the overall response was recorded as CR/CRi / CRi, CRh until documented relapse, or death from any cause, whichever occurred first, assessed up to 15 years
Duration of response (time from first tumor assessment at which the overall response was recorded as CR/CRi / CRi, CRh (AML) until documented relapse, or death from any cause, whichever occurred first.
From first tumor assessment at which the overall response was recorded as CR/CRi / CRi, CRh until documented relapse, or death from any cause, whichever occurred first, assessed up to 15 years
Overall survival
時間枠:Up to 15 years
The length of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, that patients diagnosed with the disease are still alive. In a clinical trial, measuring the overall survival is one way to see how well a new treatment works. Also called OS.
Up to 15 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。

スポンサー

捜査官

  • 主任研究者:Ryotaro Nakamura、City of Hope Medical 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 (推定)

2026年12月14日

一次修了 (推定)

2027年4月16日

研究の完了 (推定)

2027年4月16日

試験登録日

最初に提出

2026年4月29日

QC基準を満たした最初の提出物

2026年5月6日

最初の投稿 (実際)

2026年5月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月13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6日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

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

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。

購読する