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Clinical Trials in the USA / NCT05306288
Active, not recruiting Observational

CASCADE-LUNG: Cancer Screening Assay Using DELFI; A Clinical Validation Study in Lung

NCT05306288 · tracked via the Priya Life Science USA tracker
Sponsor
Delfi Diagnostics Inc.
Phase
Observational
Started
2022-04-07
Last updated
2026-03-19

Condition(s) studied

Lung Cancer

Investigational drug(s) / intervention(s)

Blood Sample Collection

Blood Sample Collection: Subjects enrolled in DELFI-L201 will have blood specimens collected (\~30 mL) at enrollment or up to 30 days after enrollment.

Study summary

CASCADE-LUNG is a multisite, prospective, observational, blood specimen collection study in the elevated-risk lung cancer screening population. The primary objective is to demonstrate the performance characteristics, including sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the DELFI Lung Cancer Screening Test (DLCST) for the detection of pathologically-confirmed lung cancer in a screening population using LDCT, pathology, and follow-up as the reference method.

Eligibility

Sex
ALL
Min age
50 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * All subjects 1. Ability to understand and provide written informed consent 2. Age ≥ 50 years 3. Current or former smoker 4. ≥ 20 pack-years (pack years = number of packs per day × number of years smoked) 5. An initial or annual follow-up lung cancer screening chest CT planned/scheduled within 30 days after enrollment (i.e., enrollment chest CT scan) Exclusion Criteria: * All subjects 1. Evidence of any diagnosed cancer (including prior lung cancer) other than non-melanoma skin cancer or carcinoma in situ within 2 years prior to enrollment 2. Prior systemic therapy, definitive therapy, radiation, or surgical resection for any cancer diagnosis within 2 years prior to enrollment (with the exception of surgery for nonmelanoma skin cancer and biopsies) 3. Any history of hematologic malignancy or myelodysplasia within 2 years prior to enrollment 4. Any history of organ tissue transplantation 5. Any history of blood product transfusion within 120 days prior to enrollment 6. Current pregnancy 7. Any condition that in the opinion of the Investigator should preclude the participant's participation in the study 8. Past or current participation in any clinical study sponsored by DELFI Diagnostics or any history of a LDT (Laboratory Developed Test) for early detection of lung cancer by DELFI Diagnostics

Primary outcome measure(s)

Trial sites (67)

FacilityCityRegionStatus
Cullman Clinical Trials Cullman Alabama
Science 37 (nationwide digital enrollment) Culver City California
Providence Facey Medical Foundation Mission Hills California
Hoag Hospital Newport Beach California
Paradigm Clinical Research Center, Inc. Redding California
San Francisco VA San Francisco California
Clinical Research of California LLC Walnut Creek California
SCL Health Research Institute, St. Mary's Grand Junction Colorado
Paradigm Clinical Research Center Wheat Ridge Colorado
Stamford Health Stamford Connecticut
Advanced Research Boynton Beach Florida
Morton Plant Hospital Clearwater Florida
SIMEDHealth, LLC Gainesville Florida
Galenus Group Lehigh Acres Florida
Renstar Medical Research Ocala Florida
United Medical Research Port Orange Florida
American Clinical Trials, LLC. Acworth Georgia
Centricity Research Columbus Piedmont Columbus Georgia
ClinCept, LLC Columbus Georgia
Coastal Heritage Clinical Research Hinesville Georgia
Centricity Research Gwinnett Pulmonology Lawrenceville Georgia
Centricity Research Rincon Pulmonology Rincon Georgia
OSF Saint Francis Medical Center Peoria Illinois
Springfield Clinic Springfield Illinois
St. Elizabeth Healthcare Edgewood Kentucky
Ochsner New Orleans Louisiana
Johns Hopkins Baltimore Maryland
Massachusetts General Hospital Cancer Center Boston Massachusetts
Henry Ford Hospital Detroit Michigan
Pulmonary Research Institute of Southeast Michigan Farmington Hills Michigan
Minneapolis VA Minneapolis Minnesota
Mayo Clinic Rochester Minnesota
Hannibal Regional Healthcare System Hannibal Missouri
Washington University St Louis Missouri
Missouri Baptist Medical Center St Louis Missouri
Somnos Clinical Research Lincoln Nebraska
Internal Medicine Associate Bridgeton New Jersey
CHRISTUS St. Vincent Regional Medical Center Santa Fe New Mexico
University of Rochester Medical Center Rochester New York
SUNY Upstate Medical University Syracuse New York

+ 27 more sites — see the full list on the official registry below.

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05306288 on ClinicalTrials.gov ↗ ← All trials in the USA