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Epcoritamab and Pola-R-mini-CHP for the Treatment of Diffuse Large B Cell Lymphoma in Elderly or Unfit Patients

2026년 7월 15일 업데이트: Jonsson Comprehensive Cancer Center

A Phase I Study of Single Agent Epcoritamab Followed by Epcoritamab Plus Pola-R-Mini-CHP for Elderly/Unfit Patients With Previously Untreated DLBCL

This phase I trial tests the safety, side effects and best dose of epcoritamab alone and epcoritamab with polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisone (pola-R- mini-CHP) for the treatment of diffuse large B cell lymphoma (DLBCL) in elderly or unfit patients. Epcoritamab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Polatuzumab vedotin is a monoclonal antibody, called polatuzumab, linked to a chemotherapy drug, called monomethyl auristatin E. Polatuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as B-cell receptors, and delivers monomethyl auristatin E to kill them. Rituximab is a monoclonal antibody. It binds to a protein called cluster of differentiation antigen 20 (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. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's DNA and may kill cancer cells. It may also lower the body's immune response. Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's DNA and may kill cancer cells. It also blocks a certain enzyme needed for cell division and deoxyribonucleic acid (DNA) repair. Prednisone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Epcoritamab alone and epcoritamab with pola-R-mini-CHP may be safe, tolerable and/or effective in treating DLBCL in elderly or unfit patients.

연구 개요

상세 설명

PRIMARY OBJECTIVE:

I. To evaluate whether the addition of epcoritamab to 4- 6 cycles of standard Pola-R-mini-CHP preceded by 2 cycles of epcoritamab monotherapy (E + Pola-mini-CHP) is tolerable and effective.

EXPLORATORY OBJECTIVE:

I. To include the use of liquid biopsy techniques, specifically PhasED-seq, to assess treatment responses.

OUTLINE:

CYCLE 1: Patients receive polatuzumab vedotin intravenously (IV) and rituximab IV on day 1 and epcoritamab subcutaneously (SC) on day 1, 8, and 15 of the 21 day cycle, in the absence of disease progression or unacceptable toxicity.

CYCLE 2: Patients receive epcoritamab on day 1, 8 and 15 of the 21 day cycle, in the absence of disease progression or unacceptable toxicity.

CYCLE 3-4: Patients receive rituximab IV, polatuzumab vedotin IV, cyclophosphamide IV, doxorubicin IV on day 1, epcoritamab SC on days 1, 8 and 15 and prednisone orally (PO) on days 1-5 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients then undergo disease assessment. Patients with complete remission receive cycles 5-6 and patients not in complete remission receive cycles 5-8.

CYCLES 5-8: Patients receive rituximab IV, polatuzumab vedotin IV, cyclophosphamide IV, doxorubicin IV and epcoritamab SC on day 1 and prednisone PO on days 1-5 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients undergo urine sample collection and brain magnetic resonance imaging (MRI) during screening and positron emission tomography (PET)/computed tomography (CT) scan and blood sample collection throughout the study.

After completion of study treatment, patients are followed up week 36, week 48 then every 12 weeks through week 94, then every 24 weeks through week 240 then every 48 weeks until 6 years after the first dose of treatment. Patients who discontinue for treatment progression are followed up every every 6 months thereafter.

연구 유형

중재적

등록 (추정된)

20

단계

  • 1단계

연락처 및 위치

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연구 장소

    • California
      • Los Angeles, California, 미국, 90095
        • UCLA / Jonsson Comprehensive Cancer Center
        • 연락하다:
        • 수석 연구원:
          • Sven De Vos

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Previously untreated, histologically confirmed DLBCL according to World Health Organization (WHO) 2016 classification

    • Documented CD20+ mature B-cell neoplasm according to WHO classification (Swerdlow et al., 2016) or WHO classification (WHO, 2008) based on representative pathology report

      • Diffuse large B-cell lymphoma note: Other double-/triple-hit lymphomas are not eligible
    • Untreated patients who transform from low grade marginal zone lymphoma (MZL)
    • Other aggressive B-non-hodgkin lymphoma (NHL):

      • Primary mediastinal (thymic) large B-cell lymphoma (PMBCL)
      • High-grade B-cell lymphoma
      • Newly diagnosed follicular lymphoma grade 3B (FL 3B)
  • At least one bi-dimensionally measurable nodal lesion, defined as > 1.5 cm in its longest dimension, or one bi-dimensionally measurable extranodal lesion, defined as > 1.0 cm in its longest diameter
  • Age > 80 years, or age 70-79 years and not considered a candidate for full-dose aggressive chemotherapy (R-CHOP) with at least one of the following:

    • Impairment in > 2 activity of daily living (ADL) component and/or
    • Impairment in > 2 instrumental activity of daily living (IADL) component and/or
    • Cumulative Illness Rating Scale for Geriatrics (CIRS-G) score of at least 1 comorbidity with a severity score of 3-4 (not including lymphoma and hematologic deficiencies due to lymphoma) or a score of 2 in > 8 comorbidities.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
  • Life expectancy of at least 24 weeks
  • No significant pulmonary comorbidities (e.g., history of pneumonitis, severe chronic obstructive pulmonary disease [COPD])
  • Left ventricular ejection fraction ≥ 45%
  • Creatinine clearance > 40 mL/min

    • Exceptions may be made for patients with creatinine clearance < 40 mL/min, provided creatinine is within normal range
  • Hemoglobin > 9 g/dL
  • Absolute neutrophil counts ≥ 1.0 × 10^9/L; growth factor support allowed in case of bone marrow involvement
  • Platelet counts ≥ 75 × 10^9/L or, in the presence of bone marrow involvement or splenomegaly, ≥ 50 × 10^9/L
  • Lymphocyte counts < 5 × 10^9/L
  • If receiving glucocorticoid treatment at screening, must be a maximum daily dose of prednisone 100 mg (or equivalent) and a total of no more than 140 mg over the last 14 days prior to the first dose of epcoritamab, unless for disease control
  • Before the first dose of epcoritamab, during the trial and for 12 months after last administration of epcoritamab, a woman must be either:

    • Not of childbearing potential: premenarchal; postmenopausal (> 45 years of age with amenorrhea for at least 12 months or any age with amenorrhea for at least 6 months and a serum follicle stimulating hormone [FSH] level > 40 IU/L or milli-International unit mIU/mL); permanently sterilized (e.g., bilateral tubal occlusion [which includes tubal ligation procedures as consistent with local regulations], hysterectomy, bilateral salpingectomy, bilateral oophorectomy); or otherwise be incapable of pregnancy
  • A man who is sexually active with a woman of childbearing potential must agree to use a barrier method of birth control (that is the use of condom) during the trial and for 12 months after receiving the last dose of epcoritamab
  • COVID-19 ELIGIBILITY CRITERIA: Subject has no known active severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection
  • COVID-19 ELIGIBILITY CRITERIA: If a subject has signs/symptoms suggestive of SARS-CoV-2 infection or have had recent known exposure to someone with SARS-CoV-2 infection, the subject must have a negative molecular (e.g., polymerase chain reaction [PCR]) test, or 2 negative antigen test results at least 24 hours apart, to rule out SARS-CoV-2 infection.

    • Note: SARS-CoV-2 diagnostic tests should be applied following local requirements/recommendations
  • COVID-19 ELIGIBILITY CRITERIA: Subjects who do not meet SARS-CoV-2 infection eligibility criteria must be screen failed and may only rescreen after they meet the following SARS-CoV-2 infection viral clearance criteria:

    • No signs/symptoms suggestive of active SARS-CoV-2 infection
    • Negative molecular (e.g., PCR) result or 2 negative antigen test results at least 24 hours apart
  • COVID-19 ELIGIBILITY CRITERIA: Patients with SARS-CoV-2 antigen or PCR testing positivity within 30 days prior to cycle 1 day 1 are not eligible
  • COVID-19 ELIGIBILITY CRITERIA: Any patient with documented SARS-CoV-2 infection within 6 months prior to planned cycle 1 day 1 must have no persistent respiratory symptoms, no evidence of residual sequelae, and a negative PCR test for SARS-CoV-2
  • COVID-19 ELIGIBILITY CRITERIA: Ongoing active bacterial, viral, fungal, mycobacterial, parasitic, or other infection requiring systemic treatment (excluding prophylactic treatment) at the time of enrollment or within the previous 2 weeks prior to the first dose of epcoritamab, including COVID-19 infection. Note that a past COVID-19 infection may be a risk factor, but if resolved and the subject is vaccinated, it may be allowable to enroll the subject

Exclusion Criteria:

  • Prior treatment for DLBCL with chemotherapy, immunotherapy, and biologic therapy

    • Exception: patients who are treated with prednisone as part of pre-phase treatment
  • Current grade > 1 peripheral neuropathy by clinical examination
  • Known or suspected chronic active Epstein-Barr virus infection
  • Subjects that have transformed from indolent (i) NHL, who have previously been treated with an anthracycline-containing regimen or a CD3-CD20 bispecific antibody
  • Patients with known history or suspected history of hemophagocytic lymphohistiocytosis (HLH)
  • Primary central nervous system (CNS) lymphoma or CNS involvement by lymphoma at screening as confirmed by mandatory magnetic resonance imaging (MRI)/computed tomography (CT) scan (brain) and, if clinically indicated, by lumbar puncture
  • Aspartate aminotransferase (AST), and/or alanine aminotransferase (ALT) > 3 × upper limit of normal (within 14 days of initiation of study treatment)
  • Total bilirubin > 1.5 × upper limit of normal, unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin (within 14 days of initiation of study treatment)

    • Patients with a documented history of Gilbert syndrome and in whom total bilirubin elevations are accompanied by elevated indirect bilirubin are eligible
  • International normalization ratio (INR) > 1.5 x upper limit of normal (ULN) in the absence of therapeutic anticoagulation (within 14 days of initiation of study treatment)
  • Partial thromboplastin time (PTT) or activated partial thromboplastin time (aPTT) > 1.5 x ULN in the absence of a lupus anticoagulant or therapeutic anticoagulant (within 14 days of initiation of study treatment)
  • Estimated creatinine clearance (CrCl) < 40 mL/min (within 14 days of initiation of study treatment)
  • Known clinically significant cardiovascular disease or significant pulmonary disease (including obstructive pulmonary disease and history of bronchospasm) including:

    • Unstable arrhythmias
    • Onset of unstable angina pectoris within 6 months of signing informed consent form (ICF)
    • Acute myocardial infarction within 6 months of signing ICF
    • Congestive heart failure (New York Heart Association Class III or IV cardiac disease and/or known decrease ejection fraction of < 45%)
    • Stroke or intracranial hemorrhage within 6 months prior to signing ICF
    • In case of any history of cardiovascular disease, a cardiology consult is required within 60 days of enrollment.
    • For patients who are ≥ 75 years old, 2 or more active cardiovascular diseases (any type, ≥ grade 2)
  • Confirmed history or current autoimmune disease or other diseases resulting in permanent immunosuppression or requiring permanent immunosuppressive therapy including, but not limited to, myocarditis, pneumonitis, myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis
  • Low-dose (≤ 10 mg/day) prednisolone (or equivalent) for rheumatoid arthritis or similar conditions is allowed
  • Received systemic immunosuppressive medications (including, but not limited to, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor agents) with the exception of corticosteroid treatment < 10 mg/day prednisone or equivalent within 2 weeks prior to first the dose of study drug
  • Positive test results for chronic hepatitis B infection (defined as positive hepatitis B surface antigen [HBsAg] serology)

    • Patients with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HBsAg) may be included if hepatitis B virus DNA is undetectable at the time of screening. These patients must be willing to undergo monthly DNA testing and appropriate antiviral therapy as indicated
  • Acute or chronic hepatitis C virus (HCV) infection

    • Patients who are positive for HCV antibody must be negative for HCV by polymerase chain reaction
  • Known human immunodeficiency virus (HIV) infection with a cluster of differentiation 4 (CD4) count greater than 200 cells/µL; HIV testing is required at screening only if required per local health authorities or institutional standards
  • History of other malignancy that could affect compliance with the protocol or interpretation of results

    • Patients with a history of curatively treated basal or squamous cell carcinoma or melanoma of the skin or in situ carcinoma of the cervix, or early-stage localized prostate cancer (Gleason score < 6 or below, Stage I or II) with no requirement for therapy at any time prior to study are eligible.
    • Patients with a malignancy that has been treated with curative intent will also be excluded unless the malignancy has been in documented remission without treatment for > 2 years before enrollment. Exception will be made for patients with a history of breast cancer that is estrogen receptor-/progesterone receptor-positive for more than 2 years before enrollment who are treated with adjuvant hormonal therapy
  • Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results or that could increase risk to the patient
  • 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 requiring treatment with IV antibiotics or hospitalization (relating to the completion of the course of antibiotics) within 4 weeks before cycle 1 day 1 (C1D1)
  • Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis
  • Recent major surgery within 4 weeks before the start of C1D1
  • Superficial lymph node biopsies for diagnosis is allowed

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Treatment (epcoritamab, pola-r-mini-CHP)
See Detailed Description
주어진 IV
다른 이름들:
  • 사이톡산
  • CTX
  • (-)-시클로포스파미드
  • 2H-1,3,2-옥사자포스포린, 2-[비스(2-클로로에틸)아미노]테트라하이드로-, 2-옥사이드, 일수화물
  • 칼록산
  • 시클로포스파미다
  • 시클로포스파마이드
  • 시클록살
  • 클라펜
  • CP 일수화물
  • CYCLO 셀
  • 사이클로블라스틴
  • 사이클로포스팜
  • 사이클로포스파미드 일수화물
  • 사이클로포스파미둠
  • 시클로포스판
  • 사이클로포스판
  • 시클로포스파늄
  • 사이클로스틴
  • 사이토포스판
  • 포스파세론
  • 제녹살
  • 제눅살
  • 레독시나
  • 미톡산
  • 네오사르
  • 리바이뮨
  • 실클로포스파미드
  • WR-138719
  • 아스타 B 518
  • B-518
  • B518
  • WR 138719
  • WR138719
  • 프린도빅스
주어진 PO
다른 이름들:
  • 델타손
  • 오라소네
  • .delta.1-코르티손
  • 1, 2-디하이드로코르티손
  • 아다손
  • 코탄실
  • 다코르틴
  • 데코르틴
  • 데코티실
  • 데코턴
  • 델타 1-코르티손
  • 델타 돔
  • 델타코르텐
  • 델타코르티손
  • 델타데히드로코르티손
  • 델티슨
  • 델타
  • 이코노손
  • 리사코트
  • 메프로소나-F
  • 메타코르탄드라신
  • 메티코르텐
  • 오피솔로나
  • 파나코트
  • 파나솔-S
  • 파라코트
  • 페리고 프레드니손
  • 프레드
  • 프레디코르
  • 앞머리
  • 프레드니센-M
  • 프레드니코트
  • 프레드니딥
  • 프레드니롱가
  • 예측
  • 프레드니손 인텐솔
  • 프레드니소눔
  • 프레드니톤
  • 프로미펜
  • 라요스
  • 세르비손
  • SK-프레드니손
주어진 IV
다른 이름들:
  • 리툭산
  • 맙테라
  • ABP 798
  • BI 695500
  • C2B8 단클론항체
  • 키메라 항-CD20 항체
  • CT-P10
  • IDEC-102
  • IDEC-C2B8
  • IDEC-C2B8 단클론항체
  • 단클론항체 IDEC-C2B8
  • PF-05280586
  • 리아브니
  • 리툭시맙 ABBS
  • 리툭시맙 ARRX
  • 리툭시맙 바이오시밀러 ABP 798
  • 리툭시맙 바이오시밀러 BI 695500
  • 리툭시맙 바이오시밀러 CT-P10
  • 리툭시맙 바이오시밀러 GB241
  • 리툭시맙 바이오시밀러 IBI301
  • 리툭시맙 바이오시밀러 JHL1101
  • 리툭시맙 바이오시밀러 PF-05280586
  • 리툭시맙 바이오시밀러 RTXM83
  • 리툭시맙 바이오시밀러 SAIT101
  • 리툭시맙 바이오시밀러 SIBP-02
  • 리툭시맙 바이오시밀러 TQB2303
  • 리툭시맙 PVVR
  • 리툭시맙-arrx
  • 리툭시맙-pvvr
  • RTXM83
  • 루시언스
  • 트룩시마
  • 릭사톤
  • 익다르
  • 맘타스
  • 리툭시맙-abbs
  • BI-695500
  • BI695500
  • 블리치마
  • IDEC 102
  • IDEC102
  • PF 05280586
  • PF05280586
  • 리템비아
  • 리툭시맙-블릿
  • 리툭시맙-라이트
  • 리툭시맙-릭사
  • 리툭시맙-릭시
  • 리치묘
  • RTXM-83
  • ABP-798
  • ABP798
  • CT P10
  • CTP10
  • GP 2013
  • GP-2013
  • GP2013
  • 리툭시맙 바이오시밀러 GP2013
주어진 IV
다른 이름들:
  • 아드리아블라스틴
  • 하이드록시다우노마이신
  • 하이드록실 다우노루비신
  • 하이드록실다우노루비신
PET 스캔을 받다
다른 이름들:
  • 의료 영상, 양전자 방출 단층 촬영
  • 애완 동물
  • PET 스캔
  • 양전자 방출 단층 촬영 스캔
  • 양전자 방출 단층 촬영
  • PT
  • 양전자방출단층촬영(시술)
CT 스캔을 받다
다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
혈액 및 소변 검체 채취
다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
주어진 IV
다른 이름들:
  • DCDS4501A
  • ADC DCDS4501A
  • 항체-약물 접합체 DCDS4501A
  • FCU 2711
  • 폴라투주맙 베도틴-피크
  • 폴리비
  • RG7596
  • 로 5541077-000
  • FCU-2711
  • FCU2711
  • RG 7596
  • RG-7596
뇌 MRI를 받다
다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
주어진 SC
다른 이름들:
  • GEN3013
  • 항-CD20/CD3 이중특이적 항체 GEN3013
  • 듀오바디-CD3xCD20
  • Epcoritamab-bysp
  • 엡킨리
  • 3013세대
  • GEN-3013
  • 텝킨리

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Progression free survival
기간: From initiation of treatment to disease progression based on the investigator-based assessments per Lugano criteria or death due to any causes, up to 6 years
Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
From initiation of treatment to disease progression based on the investigator-based assessments per Lugano criteria or death due to any causes, up to 6 years

2차 결과 측정

결과 측정
측정값 설명
기간
Overall response rate
기간: Up to 6 years
Defined as the proportion of patients achieving a complete response (CR) or partial response (PR) based on Lugano criteria. CR defined as the disappearance of all evidence of disease based on Lugano critera. PR defined as a ≥ 50% reduction in tumor burden based on Lugano criteria. Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
Up to 6 years
Duration of response
기간: From the first documentation of CR or PR to disease progression or death, up to 6 years
Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
From the first documentation of CR or PR to disease progression or death, up to 6 years
Overall survival
기간: From enrollment until death due to any cause, up to 6 years
Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
From enrollment until death due to any cause, up to 6 years
Incidence and severity of adverse events
기간: Up to 6 years
95% confidence intervals will be generated.
Up to 6 years
Incidence and severity of changes in laboratory values
기간: Up to 6 years
95% confidence intervals will be generated.
Up to 6 years
Incidence of dose interruptions, delays, and discontinuations
기간: Up to 6 years
95% confidence intervals will be generated.
Up to 6 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

협력자

수사관

  • 수석 연구원: Sven De Vos, UCLA / Jonsson Comprehensive Cancer Center

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 12월 8일

기본 완료 (추정된)

2030년 10월 8일

연구 완료 (추정된)

2031년 10월 8일

연구 등록 날짜

최초 제출

2026년 7월 15일

QC 기준을 충족하는 최초 제출

2026년 7월 15일

처음 게시됨 (실제)

2026년 7월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 20일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 15일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

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아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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