一项研究,用于评估单独使用GDC-4198并结合Giredestrant与Abemaciclib和Giredestrant的效果,对具有局部晚期或转移性雌激素受体阳性(ER+)的参与者,人类表皮生长因子受体受体(HER2)乳腺癌(HER2-)乳腺癌 (MoonROSE)
IB/II期多中心,开放标签,随机研究评估GDC-4198的安全性,药代动力学和活性,并与Abemaciclib和Abemaciclib和GiredEstrant相比,在本地高级或转移性雌激素受体疗法,HER2阳性,HER2-乳腺癌中的参与者中,与摄取者相比,与参与者相比,以前曾经是在以前曾在或6次进步的人,或者在6个以前曾经是在以前曾经是在以前曾在或6次均在6中均与6或6中有关
The purpose of this study is to assess the safety of GDC-4198 alone and in combination with giredestrant and also the efficacy of GDC-4198 + giredestrant versus abemaciclib + giredestrant in participants with locally advanced or metastatic ER+, HER2- breast cancer. The study consists of 2 phases: Phase Ib and Phase II. Phase Ib will evaluate the safety and pharmacokinetics (PK) of GDC-4198 alone and in combination with giredestrant. Phase II stage will compare the activity and safety of GDC-4198 and giredestrant with abemaciclib and giredestrant.
Participants from Study RGT-419B_01-101 (NCT05304962) who are experiencing clinical benefit with GDC-4198, as determined by the investigator, may enroll in this study and continue receiving GDC-4198 at their current dose level following closure of Study RGT-419B_01-101.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
研究联系人备份
- 姓名:Reference Study ID Number: GO46021 https://forpatients.roche.com/ No attachments to email below.
- 电话号码:888-662-6728 (U.S. Only)
- 邮箱:global-roche-genentech-trials@gene.com
学习地点
-
-
-
Fuzhou、中国、350014
- 招聘中
- Fujian Cancer Hospital
-
Nanning、中国、530201
- 招聘中
- Guangxi Cancer Hospital of Guangxi Medical University
-
-
SD
-
Jinan、SD、中国、250117
- 招聘中
- Shandong Cancer Hospital
-
-
Shanghai Municipality
-
Shanghai、Shanghai Municipality、中国、201321
- 招聘中
- Fudan University Shanghai Cancer Center - Pudong Campus
-
-
Tianjin Municipality
-
Tianjin、Tianjin Municipality、中国、300060
- 招聘中
- Tianjin Medical University Cancer Institute & Hospital
-
-
-
-
British Columbia
-
Vancouver、British Columbia、加拿大、V5Z 4E6
- 招聘中
- BC Cancer Vancouver Centre
-
-
Ontario
-
Toronto、Ontario、加拿大、M5G 2M9
- 招聘中
- Princess Margaret Hospital
-
-
-
-
-
São Paulo、巴西、01246-000
- 招聘中
- Instituto Do Câncer Do Estado de São Paulo Octávio Frias de Oliveira - ICESP
-
São Paulo、巴西、01323-001
- 招聘中
- Beneficencia Portuguesa de Sao Paulo
-
-
Pernambuco
-
Recife、Pernambuco、巴西、50040-000
- 招聘中
- Hospital do Cancer de Pernambuco - HCP
-
-
Rio Grande do Sul
-
Ijuí、Rio Grande do Sul、巴西、98700-000
- 招聘中
- ONCOSITE Centro de Pesquisa Clínica Em Oncologia
-
Porto Alegre、Rio Grande do Sul、巴西、90560-030
- 招聘中
- Hospital de Clinicas de Porto Alegre (HCPA) - PPDS
-
Porto Alegre、Rio Grande do Sul、巴西、90035-074
- 招聘中
- Irmandade Da Santa Casa de Misericordia de Porto Alegre
-
-
-
-
-
Dresden、德国、01307
- 招聘中
- Universitaetsklinikum Carl Gustav Carus an der TU Dresden
-
Hamburg、德国、20251
- 招聘中
- Universitatsklinikum Hamburg-Eppendorf
-
Heidelberg、德国、69120
- 招聘中
- Uniklinikum Heidelberg
-
-
Baden-Wurttemberg
-
Tübingen、Baden-Wurttemberg、德国、72076
- 招聘中
- Universitatsklinikum Tubingen
-
-
Lower Saxony
-
Hanover、Lower Saxony、德国、30625
- 招聘中
- Medizinische Hochschule Hannover
-
-
North Rhine-Westphalia
-
Essen、North Rhine-Westphalia、德国、45136
- 招聘中
- KEM - Evang. Huyssens-Stiftung Essen-Huttrop
-
-
-
-
Emilia-Romagna
-
Bologna、Emilia-Romagna、意大利、40138
- 招聘中
- Azienda Ospedaliero Universitaria Di Bologna_Policlinico S Orsola Malpighi-Via Albertoni
-
Meldola、Emilia-Romagna、意大利、47014
- 招聘中
- Istituto Romagnolo per lo Studio dei Tumori Dino Amadori - IRST S.r.l - PPDS
-
-
Lombardy
-
Bergamo、Lombardy、意大利、24127
- 招聘中
- Asst Papa Giovanni XXIII
-
Brescia、Lombardy、意大利、25123
- 招聘中
- ASST degli Spedali Civili di Brescia - Spedali Civili di Brescia
-
Milan、Lombardy、意大利、20132
- 招聘中
- Ospedale San Raffaele S.r.l. - PPDS
-
-
-
-
-
Caen、法国、14076
- 招聘中
- Centre Francois Baclesse
-
Lille、法国、59020
- 招聘中
- Centre Oscar Lambret
-
Rennes、法国、35042
- 招聘中
- Centre Eugene Marquis
-
-
Champagne-Ardenne
-
Reims、Champagne-Ardenne、法国、51100
- 招聘中
- Institut Jean Godinot
-
-
Val-de-Marne
-
Villejuif、Val-de-Marne、法国、94805
- 招聘中
- Gustave Roussy
-
-
-
-
New South Wales
-
Darlinghurst、New South Wales、澳大利亚、2010
- 招聘中
- St Vincent's Hospital Sydney
-
-
South Australia
-
Adelaide、South Australia、澳大利亚、5000
- 招聘中
- Cancer Research SA
-
-
-
-
Alabama
-
Huntsville、Alabama、美国、35805-2606
- 招聘中
- Clearview Cancer Institute - Huntsville
-
-
Arizona
-
Tucson、Arizona、美国、85724-0001
- 招聘中
- University of Arizona Cancer Center
-
-
California
-
Duarte、California、美国、91010
- 招聘中
- City of Hope
-
Irvine、California、美国、92618
- 招聘中
- City of Hope - Orange County Lennar Foundation Cancer Center
-
La Jolla、California、美国、92093-1503
- 招聘中
- UC San Diego Moores Cancer Center
-
San Diego、California、美国、92103-1911
- 招聘中
- University of California San Diego Medical Center
-
San Francisco、California、美国、94158
- 招聘中
- UCSF Helen Diller Family CCC
-
-
Colorado
-
Aurora、Colorado、美国、80124-5316
- 招聘中
- University of Colorado Cancer Center
-
-
Florida
-
Miami、Florida、美国、33136-1002
- 招聘中
- Sylvester Comprehensive Cancer Center
-
Tampa、Florida、美国、33612
- 招聘中
- Moffitt Cancer Center
-
-
Georgia
-
Atlanta、Georgia、美国、30322-1013
- 招聘中
- Winship Cancer Institute of Emory University
-
-
Illinois
-
Zion、Illinois、美国、60099
- 招聘中
- City of Hope® Cancer Center Chicago
-
-
Maine
-
Detroit、Maine、美国、48201-2013
- 招聘中
- Barbara Ann Karmanos Cancer Institute
-
-
Maryland
-
Annapolis、Maryland、美国、21401
- 招聘中
- Maryland Oncology Hematology - Annapolis
-
-
Massachusetts
-
Boston、Massachusetts、美国、02114
- 招聘中
- Massachusetts General Hospital
-
-
Missouri
-
St Louis、Missouri、美国、63110-1010
- 招聘中
- Washington University Siteman Cancer Center
-
-
New Jersey
-
New Brunswick、New Jersey、美国、08901-1914
- 招聘中
- Rutgers Cancer Institute of New Jersey
-
-
New York
-
East Patchogue、New York、美国、11772
- 招聘中
- New York Cancer & Blood Specialists
-
The Bronx、New York、美国、10461
- 招聘中
- Montefiore Einstein Cancer Center
-
-
North Carolina
-
Charlotte、North Carolina、美国、28204
- 招聘中
- Levine Cancer Institute
-
Charlotte、North Carolina、美国、28204
- 招聘中
- Novant Health Cancer Institute
-
Winston-Salem、North Carolina、美国、27103-3224
- 招聘中
- Novant Health Oncology Specialists
-
-
Ohio
-
Canton、Ohio、美国、44708
- 招聘中
- Cleveland Clinic Mercy Hospital
-
Cleveland、Ohio、美国、44195-0001
- 招聘中
- Cleveland Clinic Taussig Cancer Center
-
-
Oregon
-
Eugene、Oregon、美国、97401
- 招聘中
- Oncology Associates of Oregon, P.C
-
-
Pennsylvania
-
Hershey、Pennsylvania、美国、17033-2360
- 招聘中
- Penn State Health Milton S. Hershey Medical Center
-
Philadelphia、Pennsylvania、美国、19104
- 招聘中
- University of Pennsylvania - Abramson Cancer Center
-
Pittsburgh、Pennsylvania、美国、15213-3108
- 招聘中
- UPMC - Hillman Cancer Center
-
-
Tennessee
-
Mount Juliet、Tennessee、美国、37122
- 招聘中
- Tennesse Oncology - Mt. Juliet Clinic
-
Nashville、Tennessee、美国、37204-3609
- 招聘中
- Vanderbilt Breast Center at One Hundred Oaks
-
-
Texas
-
Dallas、Texas、美国、75246-2003
- 招聘中
- Texas Oncology (Worth) - USOR
-
-
Utah
-
Salt Lake City、Utah、美国、84013
- 招聘中
- University of Utah Huntsman Cancer Institute
-
-
Virginia
-
Norfolk、Virginia、美国、23502-2800
- 招聘中
- Virginia Oncology Associates (Norfolk) - USOR
-
-
-
-
-
Barcelona、西班牙、08035
- 招聘中
- Instituto de Investigacion Oncologica Vall dHebron (VHIO) - EPON
-
Madrid、西班牙、28041
- 招聘中
- Hospital Universitario 12 de Octubre
-
Madrid、西班牙、28007
- 招聘中
- Hospital Beata Maria Ana
-
Madrid、西班牙、28007
- 招聘中
- Hospital General Universitario Gregorio Maranon
-
Valencia、西班牙、46010
- 招聘中
- Hospital Clinico Universitario de Valencia
-
-
Barcelona
-
L'Hospitalet de Llobregat、Barcelona、西班牙、08908
- 招聘中
- ICO l?Hospitalet ? Hospital Duran i Reynals
-
-
-
-
-
Seongnam-si、韩国、13620
- 招聘中
- Seoul National University Bundang Hospital
-
Seoul、韩国、03080
- 招聘中
- Seoul National University Hospital
-
Seoul、韩国、06351
- 招聘中
- Samsung Medical Center
-
Seoul、韩国、6591
- 招聘中
- The Catholic University of Korea, Seoul St. Mary's Hospital
-
Seoul、韩国、3722
- 招聘中
- Severance Hospital, Yonsei University Health System
-
Seoul、韩国、05505
- 招聘中
- Asan Medical Center.
-
-
Seoul Teugbyeolsi
-
Seoul、Seoul Teugbyeolsi、韩国、6273
- 招聘中
- Gangnam Severance Hospital, Yonsei University Health System
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Histologically and/or cytologically confirmed adenocarcinoma of the breast that is locally advanced or metastatic.
- Previously documented ER+ and HER2- tumor according to American Society of Clinical Oncology (ASCO)/ College of American Pathologists (CAP) or European Society of Medical Oncology (ESMO) guidelines or any national guidelines with criteria conforming to ASCO/CAP or ESMO guidelines.
- Disease progression during or after treatment with an approved cyclin-dependent kinase 4/6 (CDK4/6) inhibitor and approved endocrine therapy (ET) in the locally advanced or metastatic setting.
- Measurable or non-measurable evaluable, disease per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).
- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
- Life expectancy >= 6 months.
- Current participant enrolled in Study RGT-419B_01-101 who is experiencing clinical benefit from GDC-4198, as determined by the investigator, at the time of consent and enrollment in this study.
Exclusion Criteria:
- Advanced, symptomatic, visceral spread that is at risk of life-threatening complications in the short term appropriate for treatment with cytotoxic chemotherapy at time of entry into the study, as per national or local treatment guidelines.
- Have received more than one-line of therapy for locally advanced or metastatic disease.
- Have received prior chemotherapy for metastatic breast cancer.
- Treatment with an approved oral ET within 7 days prior to initiation of study drug; treatment with fulvestrant or an approved CDK4/6 inhibitor within 21 days prior to initiation of study drug.
- Malabsorption condition or other gastrointestinal (GI) conditions/surgeries that the investigator assesses may significantly interfere with enteral absorption
- History of malignancy within 3 years prior to screening, except for cancer under investigation in this study and malignancies with a negligible risk of metastasis or death.
- Known allergy or hypersensitivity to any component of the study treatments.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:顺序分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Phase Ib: Dose-Finding Stage
Participants will receive GDC-4198 as monotherapy and in combination with giredestrant, 30 milligrams (mg), orally, daily, as per a pre-defined dosing regimen during each cycle until unacceptable toxicity or disease progression and/or loss of clinical benefit. (1 cycle=28 days). Participants from study RGT-419B_01-101 will continue receiving GDC-4198 at their current dose level following closure of study RGT-419B_01-101. |
GDC-4198 will be administered orally.
其他名称:
Giredestrant will be administered orally.
其他名称:
|
|
实验性的:Phase II: Arm A
Participants will receive GDC-4198, higher dose, in combination with giredestrant, 30 mg, orally, daily, as per a pre-defined dosing regimen during each cycle until unacceptable toxicity or disease progression and/or loss of clinical benefit. (1 cycle=28 days). |
GDC-4198 will be administered orally.
其他名称:
Giredestrant will be administered orally.
其他名称:
|
|
实验性的:Phase II: Arm B
Participants will receive GDC-4198, lower dose, in combination with giredestrant, 30 mg, orally, daily, as per a pre-defined dosing regimen during each cycle until unacceptable toxicity or disease progression and/or loss of clinical benefit. (1 cycle=28 days). |
GDC-4198 will be administered orally.
其他名称:
Giredestrant will be administered orally.
其他名称:
|
|
实验性的:Phase II: Arm C
Participants will receive abemaciclib, 150 mg twice daily, in combination with giredestrant, 30 mg, orally, daily, as per a pre-defined dosing regimen during each cycle until unacceptable toxicity or disease progression and/or loss of clinical benefit. (1 cycle=28 days). |
Giredestrant will be administered orally.
其他名称:
Abemaciclib will be administered orally. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
IB期:剂量限制毒性的参与者数量(DLTS)
大体时间:从第1天到周期1的第28天(1周期= 28天)
|
从第1天到周期1的第28天(1周期= 28天)
|
|
|
第二阶段:无进展生存(PFS)
大体时间:长达36个月
|
长达36个月
|
|
|
Phase Ib: Incidence and Severity of Adverse Events (AEs)
大体时间:Up to 36 months
|
Severity of AEs determined according to the CTCAE v5.0 grading scale |
Up to 36 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
IB期:客观响应率(ORR)
大体时间:长达36个月
|
长达36个月
|
|
|
IB期:临床福利率(CBR)
大体时间:长达36个月
|
长达36个月
|
|
|
第二阶段:ORR
大体时间:长达36个月
|
长达36个月
|
|
|
第二阶段:响应持续时间(DOR)
大体时间:长达36个月
|
长达36个月
|
|
|
第二阶段:CBR
大体时间:长达36个月
|
长达36个月
|
|
|
第二阶段:整体生存(OS)
大体时间:长达36个月
|
长达36个月
|
|
|
第二阶段:6个月零12个月的OS率
大体时间:第6个月,第12个月
|
第6个月,第12个月
|
|
|
第二阶段:6个月零12个月的PFS率
大体时间:第6个月,第12个月
|
第6个月,第12个月
|
|
|
第二阶段:GDC-4198的血浆浓度
大体时间:长达36个月
|
长达36个月
|
|
|
第二阶段:GDC-4198推荐剂量
大体时间:长达36个月
|
长达36个月
|
|
|
Phase II: Incidence and Severity of Adverse Events (AEs)
大体时间:Up to 36 months
|
Severity of AEs determined according to the CTCAE v5.0 grading scale |
Up to 36 months
|
合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- GO46021
- 2025-521128-31-00 (克蒂斯)
- 2025 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
For eligible studies, qualified researchers may request access to individual patient level clinical data. See Roche's commitment to transparency of clinical study information here: https://go.roche.com/data_sharing
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.