Breast Cancer Clinical Trial

Clinical Utility of CTC Test in Medicare-Eligible Metastatic Breast Cancer Patients

Summary

The objective of the registry study is to demonstrate the clinical utility of the CELLSEARCH® CTC Test among the Medicare-Eligible metastatic Breast Cancer (mBC) patients in the United States. The objective of the present registry is to demonstrate the impact on patient management of the CELLSEARCH® CTC Test among the Medicare-eligible mBC patients. Hereto the hypothesis that the availability of CTC information provides clinicians important, timely information and impacts treatment decisions, will be tested.

This study is IDE-exempt since CELLSEARCH® CTC Test is a legally marketed device in the US, and is being used in accordance with its labeling.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patient has documented (histologically/pathologically confirmed) mBC diagnosis

Patient is at least 65 years of age at time of mBC diagnosis
Patient is male or female
Patient is being actively treated at the cancer center by a physician who uses or plans to use CTC testing on his mBC patients at lease every quarter.

Exclusion Criteria:

Patients breast cancer is secondary not primary

Study is for people with:

Breast Cancer

Study ID:

NCT02111031

Recruitment Status:

Withdrawn

Sponsor:

Janssen Diagnostics, LLC

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There are 2 Locations for this study

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Abramson Cancer Center, University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States
Thomas Jefferson University
Philadelphia Pennsylvania, 19107, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT02111031

Recruitment Status:

Withdrawn

Sponsor:


Janssen Diagnostics, LLC

How clear is this clinincal trial information?

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