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Terminated Phase 2Phase 3 Interventional

MM-302 Plus Trastuzumab vs. Chemotherapy of Physician's Choice Plus Trastuzumab in HER2-Positive Locally Advanced/Metastatic Breast Cancer Patients

ClinicalTrials.gov ID: NCT02213744

Public ClinicalTrials.gov record NCT02213744. 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 Sep 16, 2026, 3:12 AM 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 Randomized, Multicenter, Open Label Study of MM-302 Plus Trastuzumab vs. Chemotherapy of Physician's Choice Plus Trastuzumab in Anthracycline Naive Patients With Locally Advanced/Metastatic HER2-Positive Breast Cancer

Brief summary

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

This study is an open label, randomized, multicenter trial of MM-302 plus trastuzumab. The trial is designed to demonstrate whether MM-302 plus trastuzumab is more effective than the chemotherapy of physician's choice (CPC) plus trastuzumab in locally advanced/metastatic HER2-positive breast cancer patients. Patients may not have been previously treated with an anthracycline in any setting. Patients must have received prior treatment with trastuzumab in any setting, have either progressed or are intolerant to ado-trastuzumab emtansine in the metastatic or locally advanced setting, have either progressed or are intolerant to pertuzumab in the metastatic or locally advanced setting or had disease recurrence within 12 months of pertuzumab treatment in the neoadjuvant or adjuvant setting.

Study identification

NCT ID
NCT02213744
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Merrimack Pharmaceuticals
Industry
Enrollment
113 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
Jun 30, 2014
Primary completion
Nov 30, 2016
Completion
May 31, 2017
Last update posted
Jan 5, 2017

2014 – 2017

United States locations

U.S. sites
70
U.S. states
28
U.S. cities
61
Facility City State ZIP Site status
Palo Verde Cancer Center Glendale Arizona
Mayo Clinic Cancer Center Scottsdale Arizona
University of Arizona Cancer Center Tucson Arizona
St. Jude Heritage Healthcare Fullerton California
UC San Diego Moores Cancer Center La Jolla California
Ronald Reagan UCLA Medical Center Los Angeles California
Cancer Care Associates Medical Group Redondo Beach California
UCSF Medical Center San Francisco California
Sansum Clinic Santa Barbara California
Kaiser Permanent Medical Center Vallejo California
University of Colorado Cancer Center Aurora Colorado
Rocky Mountain Cancer Centers Littleton Colorado
Smilow Cancer Hospital at Yale New Haven Hospital New Haven Connecticut
Washington Cancer Institute Washington D.C. District of Columbia
Florida Cancer Specialists & Research Institute Fort Meyers Florida
Memorial Regional Hospital Hollywood Florida
Mayo Clinic Cancer Center Jacksonville Florida
Sarah Cannon Research Institute New Port Richey Florida
UF Health Cancer Center at Orlando Health Orlando Florida
Florida Cancer Research Institute Plantation Florida
University of Miami Comprehensive Cancer Center Plantation Florida
Southeastern Regional Medical Center Newnan Georgia
Northwestern University- Robert H. Lurie Comprehensive Cancer Center Chicago Illinois
Rush University Medical Center Chicago Illinois
University of Chicago Chicago Illinois
Joliet Oncology-Hematology Associates Joliet Illinois
Midwestern Regional Medical Center Zion Illinois
Indiana University Melvin and Bren Simon Cancer Center Indianapolis Indiana
McFarland Clinic PC Ames Iowa
Johns Hopkins Medicine- The Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland
Dana-Farber Cancer Institute Boston Massachusetts
St. Joseph Mercy Hospital Ann Arbor Michigan
University of Michigan Health System Ann Arbor Michigan
Minnesota Oncology Hematology Coon Rapids Minnesota
University of Minnesota- Masonic Cancer Center Minneapolis Minnesota
Mayo Clinic Cancer Center Rochester Minnesota
Saint Luke's Hospital Kansas City Missouri
Barnes-Jewish West County Hospital St Louis Missouri
Hackensack University Medical Center Hackensack New Jersey
New Mexico Cancer Care Alliance Albuquerque New Mexico
New York Oncology Hematology, P.C. Albany New York
North Shore Hematology Oncology Associates East Setauket New York
Morton Coleman MD New York New York
NYU Langone Medical Center New York New York
Montefiore Medical Center The Bronx New York
Office of Carey K. Anders Chapel Hill North Carolina
Duke Cancer Institute Durham North Carolina
Oncology Hematology Care Cincinnati Ohio
Cleveland Clinic Cleveland Ohio
Ohio State University Hospital Columbus Ohio
St. Charles Health System Bend Oregon
Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania
Bon Secours Saint Francis Hospital Cancer Center Greenville South Carolina
Greenville Health System Cancer Institute Greenville South Carolina
Tennessee Oncology Chattanooga Tennessee
The Sarah Cannon Research Institute Nashville Tennessee
Vanderbilt University Medical Center Nashville Tennessee
Texas Oncology- Central Austin Cancer Center Austin Texas
Texas Oncology - Baylor Charles A. Sammons Cancer Center Dallas Texas
Texas Oncology- Medical City Dallas Texas
Texas Oncology El Paso Texas
The Center for Cancer and Blood Disorders Fort Worth Texas
Texas Oncology-Houston Memorial City Houston Texas
The University of Texas- MD Anderson Cancer Center Houston Texas
Cancer Care Centers of South Texas San Antonio Texas
Texas Oncology Tyler Texas
Huntsman Cancer Institute Salt Lake City Utah
Virginia Oncology Associate Norfolk Virginia
Swedish Medical Center Issaquah Washington
Northwest Medical Specialties Tacoma Washington

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 39 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02213744, 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 Jan 5, 2017 · Synced Sep 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02213744 live on ClinicalTrials.gov.

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