CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,142 enrolled
Drug / intervention
MammaPrint 70-gene expression profile +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01479101
NCT01479101N/ACompleted

Prospective Neo-adjuvant REGISTRY Trial Linking MammaPrint, Subtyping and Treatment Response: Neoadjuvant Breast Registry - Symphony Trial (NBRST) (Pronounced "in Breast")

Agendia·observational·Posted Nov 24, 2011·Updated Jan 19, 2021

In Brief

An observational study evaluating MammaPrint 70-gene expression profile and BluePrint 80 gene expression profile for Breast Cancer. Completed, enrolled 1,142 participants across 76 sites.

Detailed Summary

The scope of this registry study is to measure chemosensitivity as defined by pCR (primary endpoint), or endocrine sensitivity as defined by partial response (decrease in longest tumor diameter or residual cancer burden category 1 (RCB1), a primary endpoint for neo-adjuvant endocrine therapy and a secondary endpoint for neoadjuvant chemotherapy), metastasis-free survival and relapse-free survival(secondary endpoints) in molecular subgroups, determined by the established MammaPrint, BluePrint, Targetprint and Theraprint profiles in addition to possible novel expression profiles.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsBreast Cancer
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedNov 24, 2011
Enrollment StartJul 1, 2011
Primary CompletionJan 1, 2015
Study CompletionJan 1, 2021
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 14.6 years ago

Interventions

MammaPrint 70-gene expression profileother

BluePrint 80 gene expression profileother