A Prospective Observational Study of Clinical Outcomes for the NanoString® Technologies Prosigna™ Gene Signature Assay

NCT01974856 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 201

Last updated 2015-09-16

No results posted yet for this study

Summary

The primary objective of this study is to assess the extent to which the Prosigna™ Breast Cancer Prognostic Gene Signature Assay affects the medical oncologist's treatment recommendations regarding adjuvant chemotherapy and actual treatments received for patients with early-stage breast cancer.

Conditions

Sponsors & Collaborators

  • NanoString Technologies, Inc.

    lead INDUSTRY

Principal Investigators

  • Nadia Harbeck, MD, PhD · Leitung des Brustzentrums der Universität München

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2014-10-31
Completion
2015-06-30

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01974856 on ClinicalTrials.gov