Safety and Pharmacokinetics of Atezolizumab Combination Treatments in Participants With HER2-Positive and HER2-Negative Breast Cancer
Status: | Active, not recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/17/2019 |
Start Date: | December 31, 2015 |
End Date: | October 31, 2019 |
A Phase Ib, Open-Label Study Evaluating the Safety and Pharmacokinetics of Atezolizumab (Anti−PD-L1 Antibody) in Combination With Trastuzumab Emtansine or With Trastuzumab and Pertuzumab (With and Without Docetaxel) in Patients With HER2-Positive Breast Cancer and Atezolizumab With Doxorubicin and Cyclophosphamide in HER2-Negative Breast Cancer
This is a Phase Ib, open-label, two-stage study with two active regimens in each stage
designed to evaluate the safety and tolerability of combination treatment with atezolizumab,
trastuzumab, and pertuzumab (with and without docetaxel) or atezolizumab and trastuzumab
emtansine in participants with human epidermal growth factor receptor 2 (HER2) positive
metastatic breast cancer (MBC) and locally advanced early breast cancer (EBC), and
atezolizumab with doxorubicin and cyclophosphamide in HER2-negative breast cancer.
designed to evaluate the safety and tolerability of combination treatment with atezolizumab,
trastuzumab, and pertuzumab (with and without docetaxel) or atezolizumab and trastuzumab
emtansine in participants with human epidermal growth factor receptor 2 (HER2) positive
metastatic breast cancer (MBC) and locally advanced early breast cancer (EBC), and
atezolizumab with doxorubicin and cyclophosphamide in HER2-negative breast cancer.
Inclusion Criteria:
- Histologically documented HER2-positive and HER2-negative (cohort E only) breast
cancer
- Metastatic breast cancer that is measurable (Stage 1) or early breast cancer with a
primary tumor size greater than (>) 2 centimeter (cm) (Stage 2)
- Eastern cooperative oncology group (ECOG) performed status of 0, 1 or 2; 0 or 1
(cohort E only)
- Life expectancy of 12 or more weeks
- Adequate hematologic and end-organ function
- Left ventricular ejection fraction greater than or equal to (>=) 50 percentage (%);
>=55% (cohort E only)
Exclusion Criteria:
- Known central nervous system (CNS) disease, except for treated asymptomatic CNS
metastases
- Leptomeningeal disease
- Pregnancy or lactation
- History of autoimmune disease
- Prior allogeneic stem cell or solid organ transplantation
- Positive test for human immunodeficiency virus (HIV)
- Active hepatitis B or hepatitis C
We found this trial at
20
sites
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Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins The name Johns Hopkins has become synonymous...
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University of Alabama at Birmingham The University of Alabama at Birmingham (UAB) traces its roots...
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Montefiore Medical Center, Advanced Women's Health Center, Clinical Trials and Research Unit; Depart
1250 Waters Place
Bronx, New York 10461
Bronx, New York 10461
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2200 East 3rd Street
Chattanooga, Tennessee 37404
Chattanooga, Tennessee 37404
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Oncology Hematology Care Our more than 60 physicians and advanced practice providers throughout neighborhood offices...
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4018 West Capitol Avenue
Little Rock, Arkansas 72205
Little Rock, Arkansas 72205
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Medical College of Wisconsin The Medical College (MCW) of Wisconsin is a major national research...
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Tennessee Oncology, PLLC Since 1976 Tennessee Oncology has been providing quality cancer care. In 2013,...
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