20000 Participants Needed

Blood Test for Lung Cancer

(PROACT-LUNG Trial)

Recruiting at 39 trial locations
AA
HN
HN
JC
Overseen ByJoye Choy, BS
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

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).

Research Team

VS

Victoria Sumner

Principal Investigator

Freenome Holdings Inc.

Eligibility Criteria

This trial is for people aged 50 or older who are current or former smokers with a history of smoking at least 20 packs a year. Participants must understand and agree to sign consent forms.

Inclusion Criteria

Are you 50 years or older?
You have been diagnosed with Lung Cancer
You have been diagnosed with Healthy Subjects
See 4 more

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Blood Sample Collection

Blood samples are collected from participants for the Freenome Multiomics Blood Test

1 day
1 visit (in-person)

Standard-of-Care Screening

Participants undergo a routine, standard-of-care screening Low-Dose Computed Tomography (LDCT)

1 day
1 visit (in-person)

Follow-up

Participants are monitored for safety and effectiveness after screening, with data collection on diagnostic tests and procedures related to lung cancer diagnosis

24 months

Treatment Details

Trial OverviewThe study is testing the effectiveness of a new blood test designed to detect lung cancer early in high-risk individuals, alongside their routine low-dose CT scans used for screening.

Find a Clinic Near You

Who Is Running the Clinical Trial?

Freenome Holdings Inc.

Lead Sponsor

Trials
5
Recruited
78,500+