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Evaluate the Clinical Performance of the Flow Cytometry - FlowPath Lung Test as a Sensitive and Specific Non-invasive Diagnostic of Sputum Samples to Identify/Detect the Presence of Lung Cancer in High-risk Individuals Who Have Existing Lung Nodules, 6 to <30 mm in Diameter, Determined by LDCT.
RECRUITINGN/ASponsored by bioAffinity Technologies Inc.
Actively Recruiting
PhaseN/A
SponsorbioAffinity Technologies Inc.
Started2026-02-25
Est. completion2029-04-01
Eligibility
Age50 Years – 80 Years
Healthy vol.Accepted
Locations3 sites
View on ClinicalTrials.gov →
NCT07168993
Summary
Evaluate FlowPath Lung Diagnostic Test of Sputum Samples to Detect the Presence of Lung Cancer in High-risk Individuals Who Have Existing Lung Nodules, \>6 to \<30 mm in Diameter, Determined by LDCT.
Eligibility
Age: 50 Years – 80 YearsHealthy volunteers accepted
Inclusion Criteria: 1. Is able to give signed informed consent and comply with study requirements. 2. Is high risk for getting lung cancer: 1. ≥50 - 80 years of age. 2. current smoker with smoking history of at least 20 pack-years or current non-smoker with smoking history of at least 20 pack-years who quit smoking within the past 15 years. 3. Has a \>6 to \<30 mm diameter lung nodule (found by lung cancer screening or found incidentally by CT scan) as determined by CT and is willing to provide a sputum sample for FlowPath Lung test within 6 weeks of the prestudy baseline CT scan. 3a) Nodule is either new, increasing, or stable for ≤ 6 months. 3b) In cases where a person has multiple nodules as determined by CT scan, the subject's most suspicious nodule is \>6 to \<30 mm in diameter. 4\) Is willing to provide contact information to the study PI or the treating physician(s) who can release required medical information related to SOC follow-up. Exclusion Criteria: 1. Is unable to cough with sufficient exertion to produce a sputum sample (e.g., due to severe obstructive lung disease). 2. The dominant nodule is ground glass or part solid as determined by CT scan. 3. Has 5 or more nodules sized \>4 mm. 4. The nodule sized \>6 to \<30 mm in diameter is a distal (subsegmental) endobronchial nodule or a perifissural nodule. 5. Is immunosuppressed. 6. Has rheumatoid arthritis. 7. Had lung cancer diagnosis in the past 5 years or any other cancer (other than non-melanoma skin cancer) in the past 2 years. A subject on long-term medications used for prevention of cancer, such as Tamoxifen for breast cancer, is not excluded. 8. Has angina with minimal exertion. 9. Is currently pregnant or planning on becoming pregnant during this study.
Conditions3
CancerLung CancerLung Cancer (Diagnosis)
Locations3 sites
Pennsylvania
1 siteClinical Research Associates of Central Pennsylvania
DuBois, Pennsylvania, 15801
Texas
2 sitesAudie Murphy VA Medical Center
San Antonio, Texas, 78234
Brooke Army Medical Center
San Antonio, Texas, 78234
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Actively Recruiting
PhaseN/A
SponsorbioAffinity Technologies Inc.
Started2026-02-25
Est. completion2029-04-01
Eligibility
Age50 Years – 80 Years
Healthy vol.Accepted
Locations3 sites
View on ClinicalTrials.gov →
NCT07168993