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Clinical Trials/NCT02078570
NCT02078570
Unknown
Not Applicable

Breast Cancer Biomarker Sample Collection for the dtectDx v2 Assay Proof of Concept Protocol

Provista Diagnostics, Inc12 sites in 1 country500 target enrollmentMarch 2014
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Provista Diagnostics, Inc
Enrollment
500
Locations
12
Primary Endpoint
Modified Quantitative Protein Algorithmic Score (QPAS)
Last Updated
9 years ago

Overview

Brief Summary

The major purpose of this study is to evaluate a laboratory developed test that measures multiple breast cancer-specific biomarker proteins and multiple antibodies in your blood samples. The biomarker and antibody results along with your personal medical profile will be evaluated to determine your risk for the presence of a malignancy in the breast as compared to your breast evaluation assessment conducted by your physician.

Registry
clinicaltrials.gov
Start Date
March 2014
End Date
July 2017
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult women from 25 years of age to below 75 years of age
  • Breast evaluation results of ACR BI-RADS® Category 3 or 4 by imaging and physicians clinical and radiological evaluation
  • Study visit and blood collection within 4 weeks (28 days) of ACR BI-RADS assessment
  • Patient agrees to with additional health data being gathered at 6 months post assessment for diagnostic follow-up
  • Samples collected under IRB approval and Informed Consent
  • Testing performed under IRB approval or waiver (as applicable)
  • Previous approved procedures to enroll patients: breast augmentation \& cyst aspiration

Exclusion Criteria

  • Adults from 76 years of age or older and below 25 years of age
  • Final breast evaluation results other than a ACR BI-RADS Category 3 or 4
  • Subjects that have had a breast biopsy performed during the 6 months prior to the study visit
  • Samples not collected under IRB approval and Informed Consent
  • Testing not performed under IRB approval or waiver (as applicable)
  • Prior breast cancer diagnosis.

Outcomes

Primary Outcomes

Modified Quantitative Protein Algorithmic Score (QPAS)

Time Frame: 6 Months

Demonstrate proof-of-concept for use of the dtectDx-Breast Assay to assess likelihood of breast cancer malignancy in conjunction with the physicians clinical and radiological evaluations.

Quantitative Protein Algorithmic Score (QPAS)

Time Frame: Baseline

Part I: Establish an acceptable algorithm for the generation of a single numerical score from the combination of the 10 cancer biomarkers that comprise the dtectDx Breast v2.0 Assay Part II: Define a numerical score cutoff that differentiates malignant from nonmalignant breast cancer in this population of woman

Secondary Outcomes

  • QPAS relative to BI-RADS(Baseline)

Study Sites (12)

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