Clinical trial · Observational
TR(ACE) Assay Clinical Specimen Study
Evaluation of the TR(ACE) Assay for the Ability to Aid in Monitoring Disease Progress, Response to Therapy or for Recurrent or Residual Disease for Patients With Previously Diagnosed Cancers (Stage III and IV Lung and Stage IV Breast)
NCT02934360CI-TRIAL-00031243unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Neoplasms | Breast Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TR(ACE) Assay Testing | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- 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
- interventionNames
- Device: TR(ACE) Assay Testing
- label
- Breast Cancer
- description
- Previously diagnosed stage IV breast cancer subjects will provide serial plasma specimens and clinical assessment information over time.
- interventionNames
- Device: TR(ACE) Assay Testing
Primary outcomes (1)
- measure
- Clinical Assessment change
- timeFrame
- Standard of care (approximately every 6 weeks to 3 months) for 6- 9 months
- description
- Standard of care physician's clinical assessment of disease progression or response compared to previous visit
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.