- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07524855
A Study of JNJ-101684362 (HLD-0117) in Patients With Metastatic Breast Cancer (HLD-0117)
A Phase 1 Study of JNJ-101684362 (HLD-0117) in Patients With Estrogen Receptor Positive (ER+) Metastatic Breast Cancer (MBC)
The purpose of this study is to find out the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDEs) of JNJ-101684362 (HLD-0117), to evaluate the safety of JNJ-101684362 (HLD-0117) , and how well the participants can tolerate it in Part 1 (dose escalation) of the study.
연구 개요
연구 유형
등록 (추정된)
단계
- 1단계
연락처 및 위치
연구 연락처
- 이름: Study Contact
- 전화번호: 844-434-4210
- 이메일: Participate-In-This-Study1@its.jnj.com
연구 장소
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Connecticut
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New Haven, Connecticut, 미국, 06510
- 모병
- Yale University School Of Medicine
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Florida
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Sarasota, Florida, 미국, 34236
- 모병
- Florida Cancer Specialists
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Massachusetts
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Boston, Massachusetts, 미국, 02114
- 모병
- Massachusetts General Hospital
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Tennessee
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Nashville, Tennessee, 미국, 37203
- 모병
- SCRI Oncology Partners
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Texas
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San Antonio, Texas, 미국, 78229
- 모병
- South Texas Accelerated Research Therapeutics, LLC (START)
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Virginia
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Fairfax, Virginia, 미국, 22031
- 모병
- Next Virginia
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Adelaide, 호주, 5000
- 모병
- Cancer Research SA
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
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Female (assigned at birth), greater than or equal to (>=) 18 years old, and able to provide informed consent
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Histologically confirmed metastatic or locally advanced breast cancer
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Postmenopausal status defined by surgical or natural menopause, or ovarian suppression with a GnRH agonist
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Prior therapy including
- Must have received at least one endocrine therapy in the metastatic setting.
- Must have received at least one cyclin-dependent kinase (CDK) 4/6i, either in the adjuvant and/or metastatic setting.
- For Part 1 and Part 2 Cohorts 2A, 2B, 2C, and 2D: Participants may have received up to two prior distinct cytotoxic regimens (for example, taxanes, antibody-drug conjugates (ADCs), etc.) in the metastatic setting, unless discussed and approved by the medical monitor.
- For Part 2 Cohort 2E: Participants must have received more than two prior distinct cytotoxic regimens (for example, taxanes, ADCs, etc.) in the metastatic setting.
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Radiologic disease progression on the most recent therapy
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Patients must have disease evaluable per response evaluation criteria in solid tumors (RECIST) v1.1
- For Part 1 and Part 2B, 2C, and 2E: Participants may have either evaluable or measurable disease per RECIST v1.1.
- For Part 2 Cohort 2A: Participants should have measurable soft tissue disease per RECIST v1.1.
- For Part 2 Cohort 2D: Participants should have evaluable but not measurable disease.
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Willingness to provide baseline and on-treatment tumor biopsies, unless not feasible or medically appropriate
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For Part 1 and Part 2 (all cohorts):
- Participants must have documented >=10% ER staining and human epidermal growth factor receptor 2 (HER2) negative (per american society of clinical oncology [ASCO] college of american pathologists [CAP] guidelines) on the most recent tumor biopsy sample obtained.
- For Part 2 Cohort 2B: Participants must have recent estrogen receptor 1 gene (ESR1) wild type from tumor or circulating tumor deoxy ribonucleic acid (ctDNA) testing performed after the most recent endocrine therapy prior to enrollment.
- For Part 2 Cohort 2C: Participants must have ESR1 mutation detected from tumor or ctDNA testing performed prior to enrollment.
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Eastern cooperative oncology group (ECOG) performance status 0-1 and life expectancy of at least 3 months
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Adequate organ function Recovery from prior therapy-related toxicities to Grade <=1 (except alopecia; neuropathy and endocrinopathies <=Grade 2)
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Ability to swallow oral medication and comply with study procedures
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Stable dose (>=30 days) of bisphosphonates or denosumab, if applicable
Exclusion Criteria:
- Participants with Inflammatory breast cancer or leptomeningeal disease or brain metastases, with the exception of patients with definitively treated brain metastases that are clinically stable and asymptomatic for >2 weeks and who are off or receiving low-dose corticosteroid treatment (<=10 mg prednisone or equivalent) for at least 2 weeks prior to start of study treatment.
- Recent major bleeding or uncontrolled bleeding disorder
- Ongoing corticosteroid use >10 mg/day (prednisone equivalent)
- Recent anticancer or investigational therapy within 14 days (28 days for fulvestrant)
- Untreated or unstable spinal cord compression
- Significant cardiovascular disease within 6 months or ongoing uncontrolled cardiac conditions
- Active or uncontrolled infection (controlled HIV or treated hepatitis C allowed)
- Uncontrolled renal, pancreatic, or liver disease (excluding stable conditions such as Gilbert's syndrome or liver metastases)
- Another malignancy requiring treatment within 2 years (except low-risk, curatively treated cancers)
- Major surgery within 28 days
- Any condition that may interfere with safety or study compliance
- Pregnancy or breastfeeding
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 순차적 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Arm 1
JNJ-101684362 (HLD-0117): Participants with estrogen receptor positive (ER+) metastatic breast cancer (MBC) will receive JNJ-101684362 (HLD-0117) orally once daily as monotherapy in Part 1 until recommended dose(s) for expansion has been developed. Participants in Part 2 will receive JNJ-101684362 (HLD-0117) at the RP2Ds developed in Part 1. |
A treatment cycle consists of 28 days. Treatment may continue until disease progression or study discontinuation (withdrawal of consent, intercurrent illness, unacceptable adverse event or any other changes unacceptable for further treatment, etc.) |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Dose Limiting Toxicities (DLTs)
기간: 28 days
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Frequency of dose-limiting toxicities (DLTs) |
28 days
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AEs, ECGs, Labs and Clinical Changes
기간: 28 days
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Frequency and severity of adverse events (AEs) and abnormal electrocardiogram (ECG), laboratory and clinical changes from baseline |
28 days
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Objective response rate (ORR)
기간: 56 Days
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Objective response rate (ORR) per RECIST in evaluable patients |
56 Days
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Duration of response (DOR)
기간: 28 days
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DOR is defined as the time from the first occurrence of a documented objective response to disease progression or death from any cause, whichever occurs first. |
28 days
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Progression-free survival (rPFS)
기간: 56 days
|
Radiographic progression-free survival (rPFS) |
56 days
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Disease Control Rate (DCR)
기간: 24 weeks
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Disease Control Rate (DCR) |
24 weeks
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Clinical Benefit Rate (CBR)
기간: 24 weeks
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CBR is defined as the proportion of patients who achieve partial response (PR) or complete response (CR), or stable disease (SD) lasting at least 24 weeks, as assessed according to RECIST v1.1. |
24 weeks
|
공동 작업자 및 조사자
수사관
- 연구 책임자: Janssen Research & Development, LLC Clinical Trial, Janssen Research & Development, LLC
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- HLD-0117-ONC-101
- HLD-0117-ONC-101 (기타 식별자: Janssen Research & Development, LLC)
- 2026-527749-23-00 (레지스트리 식별자: EUCT number)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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