Tesetaxel Plus 3 Different PD-(L)1 Inhibitors in Patients With Triple-Negative MBC and Tesetaxel Monotherapy in Patients With HER2-Negative MBC

NCT ID: NCT03952325

Last Updated: 2021-07-30

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 294 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-07-09
• Study Completion Date: 2021-06-23

Brief Summary

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.

Detailed Description

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).

Cohort 2:

Approximately 60 elderly patients with HER2-negative MBC who have not received prior chemotherapy for advanced disease will receive tesetaxel monotherapy dosed orally at 27 mg/m2 Q3W. The primary efficacy endpoints for Cohort 2 are ORR and PFS in patients with HR-positive, HER2-negative disease. The secondary efficacy endpoints are ORR and PFS in patients with triple-negative disease, DoR and OS.

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 dosed orally at 27 mg/m2 Q3W. The primary efficacy endpoints for Cohort 3 are ORR and PFS in patients with HR positive, HER2-negative disease. The secondary efficacy endpoints are ORR and PFS in patients with triple negative disease, DoR and OS.

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort 1, Arm A: Tesetaxel plus nivolumab

Group Type: EXPERIMENTAL

Tesetaxel

Intervention Type: DRUG

Tesetaxel at 27 mg/m2 orally Q3W

Nivolumab

Intervention Type: DRUG

Nivolumab at 360 mg by intravenous infusion Q3W

Cohort 1, Arm B: Tesetaxel plus pembrolizumab

Group Type: EXPERIMENTAL

Tesetaxel

Intervention Type: DRUG

Tesetaxel at 27 mg/m2 orally Q3W

Pembrolizumab

Intervention Type: DRUG

Pembrolizumab at 200 mg by intravenous infusion Q3W

Cohort 1, Arm C: Tesetaxel plus atezolizumab

Group Type: EXPERIMENTAL

Tesetaxel

Intervention Type: DRUG

Tesetaxel at 27 mg/m2 orally Q3W

Atezolizumab

Intervention Type: DRUG

Atezolizumab at 1,200 mg by intravenous infusion Q3W

Cohort 2: Tesetaxel

Group Type: EXPERIMENTAL

Tesetaxel

Intervention Type: DRUG

Tesetaxel at 27 mg/m2 orally Q3W

Cohort 3: Tesetaxel

Group Type: EXPERIMENTAL

Tesetaxel

Intervention Type: DRUG

Tesetaxel at 27 mg/m2 orally Q3W

Interventions

Tesetaxel

Tesetaxel at 27 mg/m2 orally Q3W

Intervention Type: DRUG

Tesetaxel

Tesetaxel at 27 mg/m2 orally Q3W

Intervention Type: DRUG

Tesetaxel

Tesetaxel at 27 mg/m2 orally Q3W

Intervention Type: DRUG

Nivolumab

Nivolumab at 360 mg by intravenous infusion Q3W

Intervention Type: DRUG

Pembrolizumab

Pembrolizumab at 200 mg by intravenous infusion Q3W

Intervention Type: DRUG

Atezolizumab

Atezolizumab at 1,200 mg by intravenous infusion Q3W

Intervention Type: DRUG

Tesetaxel

Tesetaxel at 27 mg/m2 orally Q3W

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• 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 1.1.

• 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

Exclusion Criteria

• 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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Odonate Therapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Joseph O'Connell, M.D.

Role: STUDY_DIRECTOR

Odonate Therapeutics, Inc.

Locations

Sarah Cannon Research Institute - Florida Cancer Specialists

Fort Myers, Florida, United States

Florida Cancer Specialists and Research Institute

St. Petersburg, Florida, United States

Florida Cancer Specialists and Research Institute - Panhandle Region

Tallahassee, Florida, United States

Florida Cancer Specialists and Research Institute

West Palm Beach, Florida, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

New York Cancer and Blood Specialists

East Setauket, New York, United States

West Cancer Center

Germantown, Tennessee, United States

Texas Oncology - Baylor Charles A. Sammons Cancer Center

Dallas, Texas, United States

Virginia Oncology Associates

Norfolk, Virginia, United States

John Hopkins Singapore International Medical Centre

Singapore, , Singapore

National Cancer Centre Singapore

Singapore, , Singapore

Asan Medical Center

Seoul, , South Korea

Countries

United States; Singapore; South Korea

Other Identifiers

ODO-TE-B202

Identifier Type: -

Identifier Source: org_study_id