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Non-covalent BTK Inhibitor Nemtabrutinib in Combination With the CD20 Monoclonal Antibody Rituximab for the Treatment of Marginal Zone Lymphoma

2026年5月12日 更新者:City of Hope Medical Center

A Phase II Study of the Non-Covalent BTK Inhibitor Nemtabrutinib in Combination With the CD20 Monoclonal Antibody Rituximab in Patients With Marginal Zone Lymphoma

This phase II trial tests the effect of nemtabrutinib in combination with rituximab in treating patients with marginal zone lymphoma. Nemtabrutinib, a non-covalent Bruton's tyrosine kinase (BTK) inhibitor, may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Giving nemtabrutinib in combination with rituximab may be safe, tolerable and/or effective in treating patients with marginal zone lymphoma.

調査の概要

詳細な説明

PRIMARY OBJECTIVES:

I. To evaluate safety and tolerability of nemtabrutinib administered in combination with rituximab (NR) in patients with marginal zone lymphoma (MZL). (Safety lead-in) II. To evaluate efficacy of nemtabrutinib administered in combination with rituximab (NR) in patients with MZL based on complete response rate. (Phase 2)

SECONDARY OBJECTIVE:

I. To evaluate efficacy of nemtabrutinib administered in combination with rituximab in patients with MZL based on overall response rate (ORR), progression free survival, duration of response, and overall survival.

EXPLORATORY OBJECTIVE:

I. To evaluate B cell receptor pathway resistance mechanisms in non-responders and patients that relapse.

OUTLINE:

Patients receive nemtabrutinib orally (PO) once daily (QD) on days 1-28 of each cycle and rituximab intravenously (IV) on days 1, 8, 15, and 22 of cycles 1 and 3 and on day 1 of cycles 5-12. Cycles repeat every 28 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. After 12 cycles, patients with a complete response (CR) or partial response (PR) may optionally continue to receive nemtabrutinib PO QD for up to an additional 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and positron emission tomography (PET)/computed tomography (CT), CT, or magnetic resonance imaging (MRI) throughout the study. Additionally, patients may optionally undergo bone marrow biopsy and tissue biopsy on study.

After completion of study treatment, patients are followed up at 30 days. Patients with CR after 24 cycles or with progressive disease (PD) after 12 cycles are followed every 3 months for up to 1 year. Patients with CR after 12 cycles may optionally follow up every 3 months for up to 2 years.

研究の種類

介入

入学 (推定)

35

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。

研究場所

    • California
      • Duarte、California、アメリカ、91010
        • City of Hope Medical Center
        • 主任研究者:
          • Geoffrey Shouse
        • 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:

  • Documented informed consent of the participant and/or legally authorized representative

    • Assent, when appropriate, will be obtained per institutional guidelines
  • Age: ≥ 18 years
  • Eastern Cooperative Oncology Group (ECOG) ≤ 2
  • Diagnosis of MZL including splenic marginal zone lymphoma (SMZL), extra nodal marginal zone lymphoma (ENMZL) and nodal marginal zone lymphoma (NMZL), established by histologic assessment
  • Requiring treatment for MZL. Patients receiving prior systemic therapy as well as treatment naïve patients are eligible

    • Local radiotherapy not exceeding a total dose of 20 Gy at least 2 weeks prior the first dose of study therapy is allowed
  • Radiographically measurable lymphadenopathy or extra nodal lymphoid malignancy (as defined by Lugano Classification for non-Hodgkin lymphoma [NHL])

    • Subjects with splenic MZL who do not meet the radiographically measurable disease criteria described herein are eligible for participation provided that bone marrow infiltration of MZL is histologically confirmed
    • Subjects with skin extranodal marginal zone lymphoma (EMZL) who do not meet the radiographically measurable disease criteria described herein are eligible provided that skin lesion measures ≥ 1.5 cm in diameter and is documented by photo or there are multiple skin lesions measuring > 1cm in diameter on the body that cannot be incorporated in one radiation field and at least one of them is histologically confirmed as MZL
    • Subjects with gastric extra nodal MZL histologically confirmed and need therapy but do not have measurable disease and in which response to treatment can be assess by multiple random gastric biopsies
    • Subjects with conjunctival EMZL who do not meet the radiographically measurable disease criteria described herein are eligible provided that conjunctival lesion measures ≥ 1 cm in diameter and is documented by photo or there are multiple conjunctival lesions measuring together > 1 5cm that cannot be treated by radiation because of previous radiation therapy, contraindications to radiation and patient refusal to receive radiation therapy. At least one of these lesions needs be histologically confirmed as MZL
  • Willing to provide a lymph node or tissue biopsy from the most recent available archival tissue or undergo an incisional or excisional lymph node or tissue biopsy

    • Subjects with splenic MZL who do not have a tumor to biopsy or an archival tumor tissue sample are eligible provided subject is willing to undergo a bone marrow biopsy or provide an archival bone marrow biopsy that was obtained before the date of the first dose of study treatment; bone marrow sample must show histologically confirmed infiltration of MZL
  • At least one of the following criteria for treatment initiation:

    • Involvement of ≥ 3 nodal sites, each with diameter of ≥ 3 cm
    • Any nodal or extra nodal tumor mass with a diameter of ≥ 5 cm
    • B symptoms (fever ≥ 38 degrees Celsius of unclear etiology, night sweats, weight loss > 10% within the prior 6 months) or other symptoms attributed to disease or specific organ involvement associated with the relapse
    • Risk of local compressive symptoms that may result in organ compromise
    • Splenomegaly or splenic lesion without splenomegaly
    • Leukopenia attributed to MZL (leukocytes < 1000/mm^3)
    • Leukemia (> 5,000 lymphoma cells/mm^3)
    • Threatened organ function, especially for extra nodal MZL
    • Requirement for transfusion or growth factor support attributed to lymphoma
    • Involvement of 2 or more extra nodal sites, with tumor/lesion in each extra nodal site ≥ 1 cm
    • Progression or relapsed within 24 months after MZL diagnosis in patients previously treated with ≥ 1 line of systemic therapy
  • Life expectancy > 3 months
  • Prior adverse events (AEs) must be resolved to grade 1
  • Without bone marrow involvement: Absolute neutrophil count (ANC) ≥ 1,000/mm^3

    • NOTE: Growth factor is not permitted within 7 days of ANC assessment unless cytopenia is secondary to disease involvement
  • With bone marrow involvement: ANC ≥ 500/mm^3

    • NOTE: Growth factor is not permitted within 7 days of ANC assessment unless cytopenia is secondary to disease involvement
  • Without bone marrow involvement: Platelets ≥ 50,000/mm^3

    • NOTE: Platelet transfusions are not permitted within 7 days of platelet assessment unless cytopenia is secondary to disease involvement.
  • With bone marrow involvement: Platelets ≥ 30,000/mm^3

    • NOTE: Platelet transfusions are not permitted within 7 days of platelet assessment unless cytopenia is secondary to disease involvement.
  • Total bilirubin ≤ 1.5 x upper limit of normal (ULN)

    • Subjects with documented history of Gilbert's syndrome and in whom total bilirubin elevations are accompanied by elevated indirect bilirubin are eligible
  • Hemoglobin ≥ 8.0 g/dL
  • Aspartate aminotransferase (AST) ≤ 2.5 x ULN or ≤ 5 x ULN in the presence of liver involvement by lymphoma
  • Alanine aminotransferase (ALT) ≤ 2.5 x ULN or ≤ 5 x ULN in the presence of liver involvement by lymphoma
  • Creatinine clearance of ≥ 45 mL/min/1.73 m^2 using the Modification of Diet in Renal Disease formula OR ≥ 45 mL/min by the Cockcroft-Gault formula
  • Seronegative for hepatitis C virus (HCV), hepatitis B virus (HBV) (surface antigen negative) OR

    • If seropositive for HBV or HCV, nucleic acid quantitation must be performed. Viral load must be undetectable.

Patients with occult or prior HBV infection (defined as negative hepatitis B virus surface antigen [HBsAg] and positive hepatitis B core antibody [HBcAb]) may be included if HBV deoxyribonucleic acid (DNA) is undetectable, if they are willing to undergo DNA testing on day 1 of every cycle and every three months for at least 12 months after the last cycle of study treatment

  • Participants with HIV are eligible if they meet ALL the following:

    • CD4 count > 350 cells/µL at screening
    • The HIV viral load is below the detectable level as per locally available testing
    • Are on a stable antiretroviral therapy (ART) regimen for at least 4 weeks prior to study entry

      • NOTE: ART includes drugs, which are NOT strong cytochrome P450 (CYP)3A4 inducers (participants receiving ART that are strong CYP3A4 inducers are not eligible to be included in the study)
    • HIV screening tests are not required unless:

      • Known history of HIV infection
      • As mandated by local health authority
    • Are compliant with their ART

      • NOTE: If the participant has had an AIDS defining opportunistic infection in the past 12 months prior to screening, they are not eligible to be included in the study
  • Person of childbearing potential (POCBP): Negative urine or serum pregnancy test

    • If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
  • Participants assigned male sex at birth:

    • If capable of producing sperm, the participant agrees to the following during the intervention period and for at least the time needed to eliminate each study intervention after the last dose of study intervention. The length of time required to continue contraception for each study intervention is:

      • Nemtabrutinib: 12 days
      • Rituximab: 3 months
      • Abstains from penile-vaginal intercourse as their preferred and usual lifestyle (abstinent on a long-term and persistent basis) and agrees to remain abstinent OR
      • Uses contraception as detailed below unless confirmed to be azoospermic (vasectomized or secondary to medical cause, documented from the site personnel's review of the participant's medical records, medical examination, or medical history interview) as detailed below:

        • Uses a penile/external condom plus nonparticipant of childbearing potential who is not currently pregnant and should also be advised of the benefit for that partner to use an additional method of contraception, as a condom may break or leak
        • Note: Participants capable of producing ejaculate whose partner is pregnant or breastfeeding must agree to use penile/external condom during each episode of sexual activity in which the partner is at risk of drug exposure via ejaculate
      • Contraceptive use by participants capable of producing sperm should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. If the contraception requirements in the local label for any of the study interventions are more stringent than the requirements above, the local label requirements are to be followed
  • Participants assigned female sex at birth:

    • A participant assigned female sex at birth is eligible to participate if not pregnant or breastfeeding, and at least one of the following conditions applies:

      • Is not a person of childbearing potential (POCBP) OR
      • Is a POCBP and:

        • Uses a contraceptive method that is highly effective (with a failure rate of < 1% per year), with low user dependency, or is abstinent from penile-vaginal intercourse as their preferred and usual lifestyle (abstinent on a long-term and persistent basis), during the intervention period and for at least the time needed to eliminate each study intervention after the last dose of study intervention. The length of time required to continue contraception for each study intervention is:

          • Nemtabrutinib: 1 month
          • Rituximab: 12 months
        • The investigator should evaluate the potential for contraceptive method failure (ie, noncompliance, recently initiated) in relationship to the first dose of study intervention. Contraceptive use by POCBPs should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. If the contraception requirements in the local label for any of the study interventions are more stringent than the requirements above, the local label requirements are to be followed.
      • Has a negative highly sensitive pregnancy test (urine or serum) as required by local regulations within 24 hours (for urine test) or 72 hours (for serum test) before the first dose of study intervention. If a urine test cannot be confirmed as negative (e.g., an ambiguous result), a serum pregnancy test is required. In such cases, the participant must be excluded from participation if the serum pregnancy result is positive
      • Abstains from breastfeeding during the study intervention period and for at least 30 days after study intervention with nemtabrutinib
      • Medical history, menstrual history, and recent sexual activity has been reviewed by the investigator to decrease the risk for inclusion of a POCBP with an early undetected pregnancy
  • Patients with gastrointestinal dysfunction and/or clinically significant medical condition of malabsorption, inflammatory bowel disease, chronic conditions which manifest with diarrhea, refractory nausea, vomiting or any other condition that will interfere significantly with drug absorption (e.g., gastric bypass surgery, gastrectomy)

Exclusion Criteria:

  • Evidence of diffuse large B-cell lymphoma (DLBCL) transformation

    • Subjects with presumptive evidence of transformation based on clinical assessment of factors such as, but not limited to, increasing lactate dehydrogenase, rapidly worsening disease, or frequent B-symptoms, must be ruled out for a transformation to a more aggressive disease, such as DLBCL
  • History of central nervous system lymphoma (either primary or metastatic) or leptomeningeal disease
  • Active graft versus host disease
  • Concurrent anticancer therapy (eg, chemotherapy, radiation therapy, surgery, immunotherapy, biologic therapy, hormonal therapy, investigational therapy, or tumor embolization)
  • Allogeneic stem cell transplant within the last 6 months, or autologous stem cell transplant within the last 3 months before the date of the first dose of study treatment
  • Receipt of anticancer medications or investigational drugs within the following intervals before the date of the first dose of study treatment:

    • < 10 weeks from completion of any radio- or toxin-immunoconjugates
    • < 4 weeks for immunotherapy
    • < 3 weeks for radiotherapy
    • < 2 weeks for any investigational agent or other anticancer medications
    • Steroids that are used for treatment of allergy or other underlying condition are permittable, but not steroids started to treat lymphoma. Subjects receiving corticosteroids must be at a dose level ≤ 10 mg/day within 7 days of the study treatment administration
  • Inadequate recovery from adverse events related to prior therapy to grade ≤ 1 (excluding grade 2 alopecia and neuropathy)
  • Prior non-covalent BTK inhibitor (prior covalent BTK inhibitors are allowed)
  • Major surgery (under general anesthesia) within 30 days prior to therapy initiation
  • Live vaccine within 30 days
  • Use of strong cytochrome P450 3A4 (CYP3A4) inhibitors or inducers within 2 weeks of the first day of study therapy
  • History of prior malignancy except:

    • Malignancy treated with curative intent and no known active disease present for ≥ 2 years prior to initiation of therapy
    • Adequately treated non-melanoma skin cancer or lentigo maligna (melanoma in situ) without evidence of disease
    • Adequately treated in situ carcinomas (e.g., cervical, esophageal, etc.) without evidence of disease
    • Asymptomatic prostate cancer managed with "watch and wait" strategy
    • Superficial bladder cancer
    • Myelodysplastic syndrome which is clinically well controlled and no evidence of the cytogenetic abnormalities characteristic of myelodysplasia on the bone marrow at screening
  • History of severe bleeding disorder defined as an ongoing congenital or acquired condition that leads to an increased likelihood of bleeding
  • Unstable cardiac disease as defined by one of the following:

    • Acute myocardial infarction (MI) within the past 6 months
    • NYHA (New York Heart Association) heart failure class III
    • Unstable angina (angina symptoms at rest) or new-onset angina (begun within the last 3 months)
    • Left ventricular ejection fraction (LVEF) < 45%
  • Corrected QT interval (QTc) prolongation (defined as a Fridericia's formula-corrected QT interval [QTcF] > 450 msecs) or other significant electrocardiogram (ECG) abnormalities including second degree atrioventricular (AV) block type II, third degree AV block, or bradycardia (ventricular rate less than 50 beats/min)
  • AIDS-defining opportunistic infection in the past 12 months prior to screening
  • History or concurrent condition of interstitial lung disease and/or severely impaired lung function
  • Arterial or venous thrombotic or embolic events such as cerebrovascular accident (including transient ischemic attacks), deep vein thrombosis or pulmonary embolism within 3 months before the start of study treatment
  • History of organ transplant
  • Known allergy/sensitivity to nemtabrutinib or any of the excipients; history of allergic reactions attributed to compounds of similar chemical or biologic composition to study agents
  • Clinically significant uncontrolled illness
  • Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at study enrollment or any major episode of infection (as evaluated by the investigator) within 4 weeks prior to the first study treatment
  • Primary or secondary central nervous system (CNS) lymphoma at the time of recruitment or history of CNS lymphoma
  • POCBP: 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
  • 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 (nemtabrutinib, rituximab)
Patients receive nemtabrutinib PO QD on days 1-28 of each cycle and rituximab IV on days 1, 8, 15, and 22 of cycles 1 and 3 and on day 1 of cycles 5-12. Cycles repeat every 28 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. After 12 cycles, patients with a CR or PR may optionally continue to receive nemtabrutinib PO QD for up to an additional 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and PET/CT, CT, or MRI throughout the study. Additionally, patients may optionally undergo bone marrow biopsy and tissue biopsy on 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
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:
  • リツキサン
  • マブセラ
  • ABP 798
  • BI 695500
  • C2B8 モノクローナル抗体
  • キメラ抗CD20抗体
  • CT-P10
  • IDEC-102
  • IDEC-C2B8
  • IDEC-C2B8 モノクローナル抗体
  • モノクローナル抗体IDEC-C2B8
  • PF-05280586
  • リアブニ
  • リツキシマブ ABBS
  • リツキシマブ ARRX
  • リツキシマブ バイオシミラー ABP 798
  • リツキシマブ バイオシミラー BI 695500
  • リツキシマブ バイオシミラー CT-P10
  • リツキシマブ バイオシミラー GB241
  • リツキシマブ バイオシミラー IBI301
  • リツキシマブ バイオシミラー JHL1101
  • リツキシマブ バイオシミラー PF-05280586
  • リツキシマブ バイオシミラー RTXM83
  • リツキシマブ バイオシミラー SAIT101
  • リツキシマブ バイオシミラー SIBP-02
  • リツキシマブバイオシミラー TQB2303
  • リツキシマブ PVVR
  • リツキシマブarrx
  • リツキシマブ-pvvr
  • RTXM83
  • ルキシエンス
  • トルキシマ
  • リクサソン
  • イクダル
  • マブタス
  • リツキシマブ-abbs
  • BI-695500
  • BI695500
  • ブリジマ
  • IDEC102
  • PF 05280586
  • PF05280586
  • リテムヴィア
  • リツキシマブブリット
  • リツキシマブの儀式
  • リツキシマブ-リクサ
  • リツキシマブ-リキシ
  • 立命
  • RTXM-83
  • ABP-798
  • ABP798
  • CT P10
  • CTP10
  • GP2013
  • GP-2013
  • リツキシマブ バイオシミラー GP2013
PET/CTを受ける
他の名前:
  • 医用画像、陽電子放出断層撮影
  • ペット
  • PETスキャン
  • 陽電子放出断層撮影スキャン
  • 陽電子放出断層撮影
  • PT
  • 陽電子放出断層撮影(手順)
骨髄生検を受ける
他の名前:
  • 骨髄の生検
  • 生検、骨髄
CTまたはPET/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PO
他の名前:
  • MK-1026
  • ARQ531
  • ARQ-531
  • ブルートン型チロシンキナーゼ阻害剤 ARQ 531
  • BTK 阻害剤 ARQ 531
組織生検を受けます
他の名前:
  • Bx
  • BIOPSY_TYPE
  • 生検

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 unacceptable toxicity (Safety lead-in)
時間枠:During cycle 1 (cycle length = 28 days)
Observed toxicities will be summarized by type, severity, and attribution.
During cycle 1 (cycle length = 28 days)
Complete response (CR) rate (Phase 2)
時間枠:Up to 3 years
Will be defined as achieving a best response of CR at any time on the study prior to any disease progression or start of other non-protocol anti-lymphoma therapy. CR rate will be estimated along with the 95% exact binomial confidence interval.
Up to 3 years

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 3 years
Will be defined as achieving a best response of either CR or partial response (PR) any time on the study prior to any disease progression or start of other anti-lymphoma therapy. ORR will be estimated along with the 95% exact binomial confidence interval.
Up to 3 years
Progression-free survival (PFS)
時間枠:From start of protocol treatment to disease relapse/progression or death due to any cause, whichever occurs earlier, assessed up to 3 years
Will be estimated using the product-limit method of Kaplan and Meier along with the Greenwood estimator of standard error, 95% confidence interval will be constructed based on log-log transformation. Median PFS will be estimated when possible.
From start of protocol treatment to disease relapse/progression or death due to any cause, whichever occurs earlier, assessed up to 3 years
Duration of response (DOR)
時間枠:From the first achievement of PR or CR to the time of disease relapse/progression or death due to any cause, whichever earlier, assessed up to 3 years
Will be estimated using the product-limit method of Kaplan and Meier along with the Greenwood estimator of standard error, 95% confidence interval will be constructed based on log-log transformation. Median DOR will be estimated when possible.
From the first achievement of PR or CR to the time of disease relapse/progression or death due to any cause, whichever earlier, assessed up to 3 years
Overall survival (OS)
時間枠:From start of protocol treatment to death due to any cause, assessed up to 3 years
Will be estimated using the product-limit method of Kaplan and Meier along with the Greenwood estimator of standard error, 95% confidence interval will be constructed based on log-log transformation. Median OS will be estimated when possible.
From start of protocol treatment to death due to any cause, assessed up to 3 years
Incidence of adverse events
時間枠:Up to 30 days after last dose of study treatment
Will be recorded and graded using the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 scale. Observed toxicities will be summarized by type, severity, and attribution.
Up to 30 days after last dose 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:Geoffrey Shouse、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16日

一次修了 (推定)

2028年5月2日

研究の完了 (推定)

2028年5月2日

試験登録日

最初に提出

2026年5月7日

QC基準を満たした最初の提出物

2026年5月7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15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12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。

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