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

NCT02395575 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2017-10-13

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the impact of the result of the Prosigna Test (assay) on the therapeutic decision of adjuvant therapy (chemotherapy and hormone therapy) in patients suffering from early-stage breast cancer.

Conditions

Sponsors & Collaborators

  • Institut Curie

    collaborator OTHER
  • NanoString Technologies, Inc.

    lead INDUSTRY

Principal Investigators

  • Roman Rouzier, MD, PhD · Institut Curie

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2016-12-31
Completion
2017-10-31

Countries

  • France

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 NCT02395575 on ClinicalTrials.gov