NCT07401797Recruiting
Specimens for Lung Cancer Panel Design
Source: ClinicalTrials.gov · Last updated 10 Feb 2026
Brief summary (registry, in English)
This is an observational study designed to determine the optimal combination of biomarkers and clinical data for the early detection, confirmation, and better treatment of lung cancer including minimizing recurrence.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 2000 (estimated)
- First submitted
- 3 Feb 2026
- Start date
- 7 Aug 2024
- Primary completion date
- 31 Dec 2029
- Lead sponsor
- Maverix Medical
- Diseases
- Lung cancer
- NCT number
- NCT07401797
What you commit to
- Study type: Observational
- Planned participants: 2000
- From 7 Aug 2024 to the primary completion date, 31 Dec 2029
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- 6.1 Criteria for the no prior cancer suspicious nodule arm
- Inclusion:
- The patient has at least one indeterminant nodule with a diameter greater than or equal to 5mm and a Mayo SPN risk greater than 5%, identified by radiology, that has not been biopsied or undergone surgery.
- The patient and the treating physician intend to follow up on the nodule with a biopsy procedure, PET scan, or active surveillance, with the procedure or next surveillance planned within the next 7 months.
- Ability to understand the study and sign an informed consent form
- Relevant clinical data accessible
- Ability and willingness to safely donate 40 mL of blood
- Ability of the site to collect and process blood per protocol Exclusion
- 1\. The patient has one or more nodules with a Mayo SPN risk over 50% or a diameter of 30mm or greater.
- 2\. The patient has received surgical prep, including antibiotics, anesthesia, etc. Fasting is not exclusionary.
- 3\. Previous cancer diagnosis of any origin. 4. Is currently pregnant 5. Is currently a prisoner or becomes a prisoner at any point during the study 6. Is under age 18, is unable to consent, or requires a different person or entity to consent on their behalf 6.2 Criteria for the previous cancer suspicious nodule arm
- Inclusion:
- 1\. The patient has at least one indeterminant nodule with a diameter greater than or equal to 5mm and a Mayo SPN risk greater than 5%, identified by radiology, that has not been biopsied or undergone surgery.
- 2\. The patient and the treating physician intend to follow up on the nodule with a biopsy procedure, PET scan, or active surveillance, with the procedure or next surveillance planned within the next 7 months.
- 3\. The patient has been in remission for a previous cancer not of lung origin for more than 5 years.
- 4\. Ability to understand the study and sign an informed consent form 5. Relevant clinical data accessible 6. Ability and willingness to safely donate 40 mL of blood 7. Ability of the site to collect and process blood per protocol Exclusion
- The patient has one or more nodules with a Mayo SPN risk over 50% or a diameter of 30mm or greater.
- The patient has received surgical prep, including antibiotics, anesthesia, etc. Fasting is not exclusionary.
- Previous cancer diagnosis in the lung (either of lung origin or metastasis to the lung).
- The treating physician believes the lung nodule is a recurrence of a previously diagnosed cancer.
- Is currently pregnant
- Is currently a prisoner or becomes a prisoner at any point during the study
- Is under age 18, is unable to consent, or requires a different person or entity to consent on their behalf
- 6.3 Criteria for the healthy volunteer arm
- Inclusion:
- Ability to understand the study and sign an informed consent form
- Relevant clinical data accessible
- Ability and willingness to safely donate up to 40 mL of blood
- The ability of the site to collect and process blood per protocol Exclusion
- 1\. Is currently pregnant 2. Is currently a prisoner or becomes a prisoner at any point during the study 3. Is under age 18, is unable to consent, or requires a different person or entity to consent on their behalf
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Maverix Medical Coordinator of this site? Confirm its status | Phoenix | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.