A Multicenter, Phase 2 Study of Tesetaxel Plus Three Different PD-(L)1 Inhibitors in Patients With Triple-Negative, Locally Advanced or Metastatic Breast Cancer and Tesetaxel Monotherapy in Elderly and Non-Elderly Adult Patients With HER2-Negative, Locally Advanced or Metastatic Breast Cancer

Odonate Therapeutics, Inc.11 个研究点分布在 3 个国家目标入组 294 人开始时间: 2019年7月9日最近更新: 2021年7月30日

适应症

干预措施

试验速览

阶段: 2 期
状态: 终止
发起方: Odonate Therapeutics, Inc.
入组人数: 294
试验地点: 11
主要终点: Cohort 1: PFS in patients with PD-L1 positive status

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

CONTESSA TRIO is a multi-cohort, multicenter, Phase 2 study of tesetaxel, an investigational, orally administered taxane, in patients with metastatic breast cancer (MBC). In Cohort 1, approximately 200 patients with triple-negative MBC who have not received prior chemotherapy for advanced disease will be randomized 1:1:1 to receive tesetaxel plus either: (1) nivolumab; (2) pembrolizumab; or (3) atezolizumab. The primary efficacy endpoints for Cohort 1 are objective response rate (ORR) and progression free survival (PFS) in patients with programmed death-ligand 1 (PD-L1) positive status. In Cohort 2, approximately 60 elderly patients with human epidermal growth factor receptor 2 (HER2) negative MBC who have not received prior chemotherapy for advanced disease will receive tesetaxel monotherapy. The primary efficacy endpoints for Cohort 2 are ORR and PFS in patients with hormone receptor (HR)-positive, HER2-negative disease. In Cohort 3, approximately 60 non-elderly adult patients with HER2-negative MBC who have not received prior chemotherapy for advanced disease will receive tesetaxel monotherapy. The primary efficacy endpoints for Cohort 3 are ORR and PFS in patients with HR positive, HER2-negative disease.

详细描述

CONTESSA TRIO is a multi-cohort, multicenter, Phase 2 study of tesetaxel, an investigational, orally administered taxane, in patients with MBC.

Cohort 1:

Approximately 200 patients with triple-negative MBC who have not received prior chemotherapy for advanced disease will be randomized 1:1:1 to receive tesetaxel dosed orally at 27 mg/m2 once every three weeks (Q3W) plus either:

Nivolumab at 360 mg by intravenous infusion Q3W;
Pembrolizumab at 200 mg by intravenous infusion Q3W; or
Atezolizumab at 1,200 mg by intravenous infusion Q3W.

Nivolumab and pembrolizumab (programmed cell death protein 1 [PD-1] inhibitors) and atezolizumab (a programmed death-ligand 1 [PD-L1] inhibitor) are immuno-oncology (IO) agents approved for the treatment of multiple types of cancer. Two of these agents, atezolizumab and pembrolizumab, have been approved by the U.S. Food and Drug Administration (FDA) as a first-line treatment for patients with triple-negative MBC. The primary efficacy endpoints for Cohort 1 are ORR and PFS in patients with PD-L1 positive status. The secondary efficacy endpoints are ORR and PFS in all patients, duration of response (DoR) and overall survival (OS).

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Female or male patients aged:
•Cohort 1: ≥ 18 years old
•Cohort 2: ≥ 65 years old
•Cohort 3: ≥ 18 to < 65 years old
•Histologically or cytologically confirmed breast cancer
•Most recent biopsy must be HER2-negative
•Cohort 1 only: Most recent biopsy must be hormone receptor (HR) (estrogen receptor and progesterone receptor) negative
•Measurable disease per RECIST 1.
•Patients with bone-only metastatic cancer must have a measurable lytic or mixed lytic-blastic lesion
•Known metastases to the CNS are permitted but not required
•Documented (including de novo): (a) locally advanced breast cancer that is not considered curable by surgery and/or radiation; or (b) metastatic breast cancer
•Disease-free interval of at least 12 months after the completion of systemic neoadjuvant or adjuvant chemotherapy for patients previously treated with systemic chemotherapy for a tumor surgically resected with curative intent
•Cohorts 2 and 3 only: Prior endocrine therapy with or without a cyclin-dependent kinase (CDK) 4/6 inhibitor unless endocrine therapy is not indicated. Any prior targeted therapies are permitted. There is no limit to the number of prior endocrine therapies.
•Cohort 1 only: At Screening, patients must have documented evidence of positive PD-L1 expression as assessed via immunohistochemistry (IHC) scoring by local, regional, or central laboratory testing
•Eastern Cooperative Oncology Group (ECOG) performance status 0, 1 or 2
•Adequate bone marrow, hepatic and renal function

排除标准

•Prior chemotherapy for locally advanced or metastatic disease
•Cohort 1 only: prior treatment with pembrolizumab, nivolumab, atezolizumab, any other PD-(L)1/PD-L2 inhibitor or a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitor
•Current evidence or history of leptomeningeal disease
•Known human immunodeficiency virus infection, unless well controlled
•Known active hepatitis B or known active hepatitis C infection
•Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with Study participation or investigational product administration or may interfere with the interpretation of Study results
•Presence of neuropathy Grade > 1
•History of hypersensitivity to any of the Study drugs or any of their ingredients, as applicable
•Cohort 1 only:
•Chronic autoimmune disease
•Evidence of active, non-infectious pneumonia (eg, pneumonia due to autoimmune or connective tissue disease)
•Treatment with a live vaccine within 30 days prior to the first dose of nivolumab, pembrolizumab or atezolizumab
•History of active tuberculosis
•Prior organ transplantation including allogeneic stem cell transplantation
•Active infection requiring systemic therapy
•Current or prior use of immunosuppressive medication within 7 days prior to Cycle 1, Day 1
•Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent
•Anticancer treatment, including endocrine therapy, radiotherapy (except stereotactic brain radiosurgery), chemotherapy or biologic therapy, ≤ 14 days prior to Enrollment
•Major surgery ≤ 28 days prior to Enrollment
•Less than 2 weeks or 5 plasma half-lives (whichever is greater) since last use of a medication or ingestion of an agent, beverage or food that is a known clinically relevant strong inhibitor or known clinically relevant inducer of the cytochrome P450 (CYP) 3A pathway

研究组 & 干预措施

Cohort 1, Arm C: Tesetaxel plus atezolizumab

Experimental

干预措施: Atezolizumab (Drug)

Cohort 1, Arm A: Tesetaxel plus nivolumab

Experimental

干预措施: Tesetaxel (Drug)

Cohort 1, Arm A: Tesetaxel plus nivolumab

Experimental

干预措施: Nivolumab (Drug)

Cohort 1, Arm B: Tesetaxel plus pembrolizumab

Experimental

干预措施: Tesetaxel (Drug)

Cohort 1, Arm B: Tesetaxel plus pembrolizumab

Experimental

干预措施: Pembrolizumab (Drug)

Cohort 1, Arm C: Tesetaxel plus atezolizumab

Experimental

干预措施: Tesetaxel (Drug)

Cohort 2: Tesetaxel

Experimental

干预措施: Tesetaxel (Drug)

Cohort 3: Tesetaxel

Experimental

干预措施: Tesetaxel (Drug)

结局指标