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Completed Phase 1 Interventional

Safety and Pharmacokinetics of Atezolizumab Combination Treatments in Participants With HER2-Positive and HER2-Negative Breast Cancer

ClinicalTrials.gov ID: NCT02605915

Public ClinicalTrials.gov record NCT02605915. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 11:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02605915
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
98 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2015 (Actual)
Primary completion
Nov 13, 2019 (Actual)
Completion
Nov 13, 2019 (Actual)
Last update posted
Feb 5, 2020

2015 – 2019

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294-3300 —
University of Arkansas for Medical Sciences; Winthrop Rockefeller Cancer Institute Little Rock Arkansas 72205 —
Joliet oncology hematology associates Joliet Illinois 60435 —
Horizon Oncology Research, Inc. Lafayette Indiana 47905 —
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21287 —
Karmanos Cancer Center; Department of Oncology Detroit Michigan 48201 —
HCA Midwest Division Kansas City Missouri 64132 —
Montefiore Medical Center, Advanced Women's Health Center, Clinical Trials and Research Unit; Depart The Bronx New York 10461 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Duke Cancer Center Durham North Carolina 27710 —
Oncology Hematology Care Inc Cincinnati Ohio 45242 —
St. Luke's University Health Network Bethlehem Pennsylvania 18015 —
Kimmel Cancer Center Thomas Jefferson University Philadelphia Pennsylvania 19107 —
Magee Womens Hospital Pittsburgh Pennsylvania 15213 —
Tennessee Oncology - Chattanooga; Tennessee Oncology - East Third Street Chattanooga Tennessee 37404 —
West Clinic Germantown Tennessee 38138 —
Tennessee Oncology Nashville Tennessee 37203 —
MD Anderson Cancer Center Houston Texas 77030 —
Cancer Therapy and Research Center CTRC at UTHSCSA San Antonio Texas 78229 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02605915, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 5, 2020 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02605915 live on ClinicalTrials.gov.

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