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.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ 1
連絡先と場所
研究連絡先
研究連絡先
- 名前:Study Contact
- 電話番号:844-434-4210
- メール:Participate-In-This-Study1@its.jnj.com
研究場所
-
-
Connecticut
-
New Haven、Connecticut、アメリカ、06510
- 募集
- Yale University School Of Medicine
-
-
Florida
-
Sarasota、Florida、アメリカ、34236
- 募集
- Florida Cancer Specialists
-
-
Massachusetts
-
Boston、Massachusetts、アメリカ、02114
- 募集
- Massachusetts General Hospital
-
-
Tennessee
-
Nashville、Tennessee、アメリカ、37203
- 募集
- SCRI Oncology Partners
-
-
Texas
-
San Antonio、Texas、アメリカ、78229
- 募集
- South Texas Accelerated Research Therapeutics, LLC (START)
-
-
Virginia
-
Fairfax、Virginia、アメリカ、22031
- 募集
- Next Virginia
-
-
-
-
-
Adelaide、オーストラリア、5000
- 募集
- Cancer Research SA
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
-
Female (assigned at birth), greater than or equal to (>=) 18 years old, and able to provide informed consent
-
Histologically confirmed metastatic or locally advanced breast cancer
-
Postmenopausal status defined by surgical or natural menopause, or ovarian suppression with a GnRH agonist
-
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.
-
Radiologic disease progression on the most recent therapy
-
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.
-
Willingness to provide baseline and on-treatment tumor biopsies, unless not feasible or medically appropriate
-
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.
-
Eastern cooperative oncology group (ECOG) performance status 0-1 and life expectancy of at least 3 months
-
Adequate organ function Recovery from prior therapy-related toxicities to Grade <=1 (except alopecia; neuropathy and endocrinopathies <=Grade 2)
-
Ability to swallow oral medication and comply with study procedures
-
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
研究計画
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:順次割り当て
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的: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.) |
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Dose Limiting Toxicities (DLTs)
時間枠:28 days
|
Frequency of dose-limiting toxicities (DLTs) |
28 days
|
|
AEs, ECGs, Labs and Clinical Changes
時間枠:28 days
|
Frequency and severity of adverse events (AEs) and abnormal electrocardiogram (ECG), laboratory and clinical changes from baseline |
28 days
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Objective response rate (ORR)
時間枠:56 Days
|
Objective response rate (ORR) per RECIST in evaluable patients |
56 Days
|
|
Duration of response (DOR)
時間枠:28 days
|
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
|
|
Progression-free survival (rPFS)
時間枠:56 days
|
Radiographic progression-free survival (rPFS) |
56 days
|
|
Disease Control Rate (DCR)
時間枠:24 weeks
|
Disease Control Rate (DCR) |
24 weeks
|
|
Clinical Benefit Rate (CBR)
時間枠:24 weeks
|
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
|
協力者と研究者
捜査官
捜査官
- スタディディレクター:Janssen Research & Development, LLC Clinical Trial、Janssen Research & Development, LLC
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
その他の研究ID番号
- HLD-0117-ONC-101
- HLD-0117-ONC-101 (その他の識別子:Janssen Research & Development, LLC)
- 2026-527749-23-00 (レジストリ識別子:EUCT number)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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
米国FDA規制機器製品の研究
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。