🔎 Trials Near Me

Home › Lung Cancer › NCT06122077

Clinical Validation of Freenome Multiomics Blood Test for Lung Cancer Screening

RecruitingObservational study

The PROACT LUNG Study: A Prospective, Observational,Clinical Validation Study of the Freenome Multiomics Blood Test for Lung Cancer Screening (FRNM-007)

Who can join

Ages 50 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Age 50 years or older within 30 days of enrollment
2. Current or former smokers with a cumulative smoking history of ≥ 20 pack-year
3. Able to comprehend and willing to sign and date the informed consent and HIPAA authorization documents

Exclusion Criteria:

1. Any active therapy for cancer, including but not limited to surgery, chemotherapy, biologic therapy, immunotherapy, and/or radiation therapy at the time of enrollment
2. History of any malignancy within prior 5 years of enrollment (except for non- melanoma skin cancer)
3. History of organ, tissue, and bone marrow transplantation
4. Screened for lung cancer or having chest CT scan 12 months before enrollment
5. Having signs and symptoms of lung cancer such as hemoptysis, superior vena cava syndrome, Cushing syndrome, and Pancoast syndrome
6. Received a blood transfusion in the 30 days preceding enrollment
7. Known to be pregnant
8. Participated or currently participating in another Freenome-sponsored clinical study
9. Participated or currently participating in a clinical research study in which an experimental medication has been administered during the 60 days preceding enrollment
10. Any condition that in the opinion of the Investigator should not be enrolled in the study

About the study

The PROACT LUNG study is a prospective multi-center observational study to validate a blood-based test for the early detection of lung cancer by collecting blood samples from high-risk participants who will undergo a routine, standard-of-care screening Low-Dose Computed Tomography (LDCT).

What is being tested

Sponsor: Freenome Holdings Inc. · Participants: 20,000 · Started: Nov 28, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT06122077

Locations in the U.S.

CaliforniaScience 37, Los Angeles
ConnecticutStamford Hospital, Stamford
FloridaHillcrest Medical Research, DeLand
Universal Axon Clinical Research, Doral
I.H.S Health, LLC, Kissimmee
United Medical Research, Port Orange
Charter Research, The Villages
Charter Research, Winter Park
GeorgiaSpeciCare, Inc, Gainesville
IllinoisUniversity of Chicago, Chicago
Walgreens, Deerfield
Springfield Clinic, LLP, Springfield
KansasAton Health, Leawood
Ascension Via Christi Wichita, Wichita
MarylandAscension St. Agnes Hospital, Baltimore
MassachusettsCape Cod Hospital, Hyannis
MississippiMemorial Hospital at Gulfport, Gulfport
NevadaRenown Regional Medical Center, Reno
New JerseyInspira Medical Center, Mullica Hill
New YorkOur Lady of Lourdes Hospital, Binghamton
North CarolinaWakemed, Raleigh
North DakotaAltru Health System, Grand Forks
OklahomaHightower Clinical, Oklahoma City
OregonOregon Health & Science University, Portland
PennsylvaniaClinical Research Associates of Central PA, DuBois
US Digestive Health at Lancaster, Lancaster
Temple University, Philadelphia
Guthrie Medical Group, Sayre
US Digestive Health at Wyomissing, Wyomissing
South CarolinaMedical University of South Carolina (MUSC), Charleston
McLeod Health, Florence
South DakotaCircle Clinical Research, Pierre
TennesseeThe Jackson Clinic, PA, Jackson
TexasHorizon Clinical Research Group, Houston
CHRISTUS Trinity Mother Frances Health System, Tyler
WisconsinAscension Columbia St. Mary's Wisconsin, Milwaukee

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.