TR(ACE) Assay Clinical Specimen Study

Biological Dynamics

Status: Unknown

Conditions: Carcinoma, Non-Small-Cell Lung; Breast Neoplasms

Treatments: Device: TR(ACE) Assay Testing

Study type: Observational

Funder types: Industry

Identifiers

NCT02934360

BioDyn-15-003

Details and patient eligibility

About

The TR(ACE) Assay is a quantitative in vitro diagnostic test run on the TR(ACE) Instrument intended for the measurement of high molecular weight human DNA from plasma as an aid to monitoring disease progression or response to therapy or recurrent or residual disease.

Full description

This study is to establish the clinical performance of the TR(ACE) Assay. Deltas of serial TR(ACE) Assay measurements will be compared to the standard of care physician clinical assessment and RECIST 1.1 criteria evaluation relative to the previous visit. Significant changes in serial TR(ACE) Assay measurements are hypothesized to correlate with disease progression or response.

Enrollment: 450 estimated patients

Sex: All

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Non-small cell lung: Male or Female Adult patient >= 21 years old
• Breast only: Female Adult patient >= 21 years old
• Previously diagnosed with one of the following cancers:

Breast or Non-small Cell Lung

• Cancer has progressed to at least Stage III or higher for lung cancer or,
• Cancer has progressed to stage IV (metastatic) breast cancer
• Participating in standard of care cancer therapy requiring frequent treatments, typically intravenous chemotherapy visits (or as determined by the standard of care for the particular cancer assessed), of a minimum of three (3) treatment visits planned in 9 months from date of enrollment where a clinical assessment will be conducted

Exclusion criteria

• Physician assessment that obtaining two extra whole blood specimens with minimum volume of 5 mL per treatment visit is contraindicated
• Stage I and II Non-small Cell Lung Cancer
• Stage I through III breast cancer
• Pregnant or planning to become pregnant during the course of the study
• Unable to obtain informed consent from subject or their legal representative
• Life expectancy is less than 9 months
• Presence of one or more of the following other chronic diseases
• Another type of cancer except for non-melanomatous skin tumors
• Autoimmune disease requiring DMARDS or Biologics
• Infectious disease requiring prolonged intravenous antibiotics or hospitalization
• Renal disease specifically those in End Stage Renal Failure
• Recent (< 3 weeks) major trauma or major surgical procedure(s) or radiation therapy prior to enrollment in the study
• Recent (< 2 months) major occlusive arterial event such as MI or CVA prior to enrollment in the study

Trial design

450 participants in 2 patient groups

Non-small cell Lung Cancer

Description:

Previously diagnosed stage III or higher non-small cell lung cancer subjects will provide serial plasma specimens and clinical assessment information over time

Treatment:

Device: TR(ACE) Assay Testing

Breast Cancer

Description:

Previously diagnosed stage IV breast cancer subjects will provide serial plasma specimens and clinical assessment information over time.

Treatment:

Device: TR(ACE) Assay Testing