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Completed No phase listed Observational

Measuring the Impact of MammaPrint on Adjuvant and Neoadjuvant Treatment in Breast Cancer Patients: A Prospective Registry

ClinicalTrials.gov ID: NCT02670577

Public ClinicalTrials.gov record NCT02670577. 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 21, 2026, 9:07 AM EDT

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

Brief summary

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

The scope of this study is to measure the impact of MammaPrint on treatment in Hormone Receptor (HR)-positive HER2-negative breast cancer patients. In addition, the impact of MammaPrint on treatment in patients with T1a/T1b and pN0/pN1 (up to 1 node), Triple Negative or HER2-positive tumors will be assessed.

Study identification

NCT ID
NCT02670577
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Agendia
Industry
Enrollment
481 participants

Conditions and interventions

Conditions

Interventions

Not listed

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
Nov 2015 (Type not available)
Primary completion
Apr 30, 2017 (Actual)
Completion
Aug 2017 (Actual)
Last update posted
Jun 27, 2018

2015 – 2017

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Desert Regional Medical Center Palm Springs California 92262 —
University of Miami Miami Florida 33442 —
St. Joseph's Women's Hospital Tampa Florida 33607 —
The Cancer Center at DeKalb Medical Decatur Georgia 30033 —
Cadence Cancer Center Warrenville Illinois 60555 —
Methodist Hospital Merrillville Indiana 46410 —
Community Healthcare System Munster Indiana 46321 —
Western Maryland Health System Cumberland Maryland 21502 —
Sparrow Cancer Center Lansing Michigan 48911 —
Essex Oncology Belleville New Jersey 07109 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Akron General Medical Center Akron Ohio 44302 —
University of Oklahoma Oklahoma City Oklahoma 73104 —
St. Mary Medical Center Langhorne Pennsylvania 19047 —
St. Clair Hospital Pittsburgh Pennsylvania 15102 —
Aurora Cancer Care Milwaukee Wisconsin 53226 —
Columbia St. Mary's Milwaukee Wisconsin — —

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 NCT02670577, 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 Jun 27, 2018 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02670577 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →