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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 Nov 2, 2026, 6:07 AM EST

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
Jul 2014 (Type not available)
Primary completion
Dec 2016 (Actual)
Completion
Jun 2017 (Estimated)
Last update posted
Jan 6, 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 6, 2017 · Synced Nov 2, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02213744 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →