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Enfortumab Vedotin, Pembrolizumab and Quemliclustat for the Treatment of Unresectable Locally Advanced and Metastatic Urothelial Cancer

2026년 9월 16일 업데이트: Fred Hutchinson Cancer Center

A Phase Ib/II Study to Evaluate the Safety and Efficacy of Enfortumab Vedotin Plus Pembrolizumab in Combination With Quemliclustat in Unresectable Locally Advanced and Metastatic Urothelial Carcinoma

This phase Ib/II trial tests the safety, side effects, and best dose of quemliclustat in combination with enfortumab vedotin and pembrolizumab, and to see how well the combination works for the treatment of bladder, renal pelvis, or ureter urothelial cancer that cannot be removed by surgery (unresectable), 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). Enfortumab vedotin is a monoclonal antibody, enfortumab, linked to an anticancer drug called vedotin. It works by helping the immune system to slow or stop the growth of cancer cells. Enfortumab attaches to a protein called nectin-4 on cancer cells in a targeted way and delivers vedotin to kill them. It is a type of antibody-drug conjugate. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Quemliclustat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving quemliclustat in combination with enfortumab vedotin and pembrolizumab and may be safe, tolerable and/or effective in treating patients with unresectable locally advanced and metastatic urothelial cancer.

연구 개요

상태

모병

개입 / 치료

상세 설명

OUTLINE:

Patients receive quemliclustat intravenously (IV) on day 1, enfortumab vedotin IV on days 1 and 8 and pembrolizumab IV on day 1 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients may undergo tumor biopsy during screening and optionally undergo throughout the study. Patients also undergo computed tomography (CT)/magnetic resonance imaging (MRI) and blood sample collection throughout the study.

After completion of study treatment, patients are followed up within 30 days and then every 12 weeks for 3 years.

연구 유형

중재적

등록 (추정된)

27

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Washington
      • Seattle, Washington, 미국, 98109
        • 모병
        • Fred Hutch/University of Washington Cancer Consortium
        • 수석 연구원:
          • Rosa Nadal Rios, MD, PhD
        • 연락하다:

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

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Participants must be at least 18 years of age on the day of signing informed consent. Participant (or legally authorized representative if applicable) provides written informed consent for trial
  • Participants must have previously untreated locally advanced or metastatic bladder cancer including bladder cancer [stage IIIB: T1-T4N2-3M0, stage IVa: T4bAnyNM0 or AnyTAnyNM1a, and stage IVB: AnyTAnyNM1b clinical stage per American Joint Commission on Cancer (AJCC)] or renal pelvis or ureter cancer [stage IV: T4Nx-0M0, AnyTN1-2M0, AnyTAnyNM1 clinical stage per AJCC]. Lymph node with ≥ 15 mm short axis or biopsy-positive for carcinoma will be considered pathologically enlarged and measurable
  • Participants must have either conventional urothelial carcinoma or urothelial carcinoma variants. A review of pathology by a local expert genitourinary (GU) pathologist is required to confirm the diagnosis. Any component (%) of non-conventional urothelial noted on tumor specimen is allowed for only histologic subtypes listed below in up to 20% of participants enrolled in this study.

    • Urothelial carcinoma with squamous differentiation
    • Urothelial carcinoma with glandular differentiation
    • Urothelial carcinoma with trophoblastic differentiation
    • Nested urothelial carcinoma
    • Tubular and microcystic urothelial carcinoma
    • Micropapillary urothelial carcinoma
    • Lymphoepithelioma-like urothelial carcinoma
    • Plasmacytoid urothelial carcinoma
    • Sarcomatoid urothelial carcinoma
    • Giant cell urothelial carcinoma
    • Lipid-rich urothelial carcinoma
    • Clear cell (glycogen rich) urothelial carcinoma
    • Poorly differentiated urothelial carcinoma
    • Squamous cell neoplasms including pure squamous cell carcinomas, verrucous carcinomas and squamous cell papilloma
  • Measurable disease by RECIST v 1.1
  • Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-2
  • Available baseline fresh biopsy tissue sample obtained in the protocol RG1712006 though clinically indicated procedures or participants must be willing to undergo a baseline research biopsy when safe and feasible
  • Participant must have an estimated life expectancy of at least 3 months
  • Hemoglobin ≥ 9 gr/dl
  • Absolute neutrophil count: ≥ 1500/ µL
  • White blood cell count: ≥ 3000/µL
  • Absolute lymphocyte count: ≥ 1000/µL
  • Platelet count: ≥ 100.000/µL (without transfusion support)
  • Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT): ≤ 2.5 x upper limit of normal (ULN)
  • Total bilirubin: ≤ 1.5 mg/dl except for patients with Gilbert's syndrome who must have a total bilirubin ≤ 3 mg/dl
  • Creatinine clearance: ≥ 30 ml/min/1.73m^2 by the method of Chronic Kidney Disease Epidemiology Collaboration (CKI-EPI) or ≥ 30 ml/min by the method of 24 hour (h) clearance of creatinine calculation
  • International Normalized Ratio (INR): < 1.5

Exclusion Criteria:

  • Participants who are receiving any other investigational agents or concurrent anticancer treatment. Participants must have adequate treatment washout period before treatment, defined as: Major surgery (≥ 4 weeks), palliative radiation therapy (≥ 1 weeks from completion of treatment if they have recovered from the acute toxic effect of radiotherapy), prior adjuvant immunotherapy (≥ 4 weeks)
  • Participants whose tumors have any % neuroendocrine or small cell histology, glandular neoplasms, urachal carcinomas, tumor of mullerian type, mesenchymal tumors or urothelial tract hematopoietic and lymphoid tumors
  • Participants considered to be medically unfit for EV-P regimen as per Investigator discretion
  • Participants with concurrent use of systemic steroids (within 10 days of enrollment), except for physiologic doses of systemic steroid replacement or local (topical, nasal, intraarticular or inhaled) steroid use
  • Participants who have experienced disease progression following neoadjuvant or adjuvant systemic therapy within 12 months prior to enrollment will not be eligible
  • Patients with Fridericia's corrected QT interval (QTcF) interval at screening of > 480 milliseconds.

    • Note: For any QTcF > 480 milliseconds on initial electrocardiogram (ECG), a follow-up ECG will be performed to confirm QTcF interval prolongation and exclude the patient from this study
  • Participants with active systemic autoimmune disease (e.g., lupus erythematosus, rheumatoid arthritis, Addison's disease, autoimmune disease associated with lymphoma, inflammatory bowel disease). Participants with autoimmune endocrine disorders controlled by medical management (e.g. thyroid disorders, type 1 diabetes, or adrenal insufficiency) will not be excluded
  • Participants who are known to be serologically positive for human immunodeficiency virus (HIV) and a CD4 count < 350 cells/microliter
  • Participants with known active hepatitis (i.e. Hepatitis B or C). Prior hepatitis (Hep) C infection is allowed as long as polymerase chain reaction (PCR) test is negative
  • Participants with clinically inactive brain metastases may be included. Participants with treated brain metastases that are no longer symptomatic and who require no treatment with corticosteroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 2 weeks must have elapsed between the end of whole-brain radiation therapy and study treatment
  • Participants with new or progressive brain metastases (less or equal of 1 cm of larger diameter) are eligible if the treating physician determines that immediate central nervous system (CNS) specific treatment is not required and is unlikely to be required for at least 4 weeks (or scheduled assessment after the first cycle of treatment), and a risk-benefit analysis (discussion) by the participant and the investigator favors participation in the clinical trial. Patients with leptomeningeal disease will be excluded
  • History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results, interfere with the participant's participation for the full duration of the trial, or is not in the best interest of the participant to participate, in the opinion of the treating investigator
  • Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy of assessment of the investigational regimen are eligible for this trial
  • Woman of childbearing potential with positive serum pregnancy test within 72 hours prior to enrollment. Active lactation is an exclusion criterion

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 (enfortumab vedotin, pembrolizumab, quemliclustat)
Patients receive quemliclustat IV on day 1, enfortumab vedotin IV on days 1 and 8 and pembrolizumab IV on day 1 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients may undergo tumor biopsy during screening and optionally undergo throughout the study. Patients also undergo CT/MRI and blood sample collection throughout the study.
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 IV
다른 이름들:
  • 키트루다
  • MK-3475
  • 람브롤리주맙
  • SCH 900475
  • MK3475
  • SCH-900475
  • BCD-201
  • 펨브롤리주맙 바이오시밀러 BCD-201
  • 펨브롤리주맙 바이오시밀러 QL2107
  • QL2107
  • GME 751
  • GME751
  • 펨브롤리주맙 바이오시밀러 GME751
  • MK 3475
  • SCH900475
  • 펨브롤리주맙 바이오시밀러 RPH-075
  • RPH 075
  • RPH-075
  • RPH075
  • 펨브 롤리 주맙 바이오시 밀러 SB27
  • SB 27
  • SB-27
  • SB27
혈액 샘플 채취
다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
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
주어진 IV
다른 이름들:
  • ASG-22CE
  • 패드체프
  • AGS 22ME
  • AGS-22M6E
  • 안티 넥틴 4 ADC ASG-22CE
  • 항-넥틴-4 단클론 항체-약물 컨쥬게이트 AGS-22M6E
  • 엔포르투맙 베도틴-ejfv
  • ASG 22CE
  • ASG22CE
종양 생검을받습니다
다른 이름들:
  • 비엑스
  • 생검_유형
Given IV
다른 이름들:
  • AB680
  • AB 680
  • AB-680
  • CD73 억제제 AB680

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Incidence of treatment related adverse events (Phase Ib)
기간: From baseline, up to 21 days after last dose of investigational product
As measured by Common Terminology Criteria for Adverse Events version (v) 6.
From baseline, up to 21 days after last dose of investigational product
Overall response rate (ORR) (Phase II)
기간: From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) v 1.1. Will calculate the count and percentage with a 95% confidence interval (CI).
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment

2차 결과 측정

결과 측정
측정값 설명
기간
ORR (Phase Ib)
기간: From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Assessed by RECIST v 1.1. Will calculate the count and percentage with a 95% CI.
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Complete response rate (Phase II)
기간: From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Assessed by RECIST v 1.1. Will calculate the count and percentage with a 95% CI.
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
Duration of response (Phase II)
기간: From response (ORR) until disease progression or unacceptable side effects or death which occurs earlier, up to 3 years after completion of study treatment
Will use Kaplan Meier method to estimate the survival curve, median and its corresponding 95% CI.
From response (ORR) until disease progression or unacceptable side effects or death which occurs earlier, up to 3 years after completion of study treatment
Progression free survival (Phase II)
기간: From date of registration to date of first documentation of progression assessed by local review or symptomatic deterioration, or death due to any cause, up to 3 years after completion of study treatment
Will use Kaplan Meier method to estimate the survival curve, median and its corresponding 95% CI.
From date of registration to date of first documentation of progression assessed by local review or symptomatic deterioration, or death due to any cause, up to 3 years after completion of study treatment
Rate of consolidative therapy with cystectomy or chemoradiation with stage 3b (Phase II)
기간: Up to 6 months
Will calculate the count and percentage with a 95% CI.
Up to 6 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

협력자

수사관

  • 수석 연구원: Rosa Nadal Rios, MD, PhD, Fred Hutch/University of Washington Cancer Consortium

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 10월 15일

기본 완료 (추정된)

2029년 7월 16일

연구 완료 (추정된)

2029년 7월 16일

연구 등록 날짜

최초 제출

2026년 6월 18일

QC 기준을 충족하는 최초 제출

2026년 6월 18일

처음 게시됨 (실제)

2026년 6월 25일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 17일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 16일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • RG1125912
  • NCI-2026-03972 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
  • FHIRB0021336 (기타 식별자: Fred Hutch/University of Washington Cancer Consortium)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

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. .