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NCT06482073Recruiting

Molecular Analysis of Suspected or High-Risk Lung Cancer to Drive Individualized Care

Molecular Analysis of Suspected or High-Risk Lung Cancer to Drive Individualized Care (INTERCEPTioN for Suspected Lung Cancer)for Suspected Lung Cancer)

Source: ClinicalTrials.gov · Last updated 8 Sept 2026

Brief summary (registry, in English)

This study evaluates the effectiveness of tumor samples in providing information about hereditary or cancer specific genetic variants that may have a role in diagnosis of cancer and to develop genetic results and medical record databank for future studies.

Status (registry)
Recruiting
Study type
Observational
Enrollment
250 (estimated)
First submitted
25 Jun 2024
Start date
24 Jun 2024
Primary completion date
1 Jul 2027
Lead sponsor
Mayo Clinic
Diseases
Lung cancer
NCT number
NCT06482073

What you commit to

  • Study type: Observational
  • Planned participants: 250
  • From 24 Jun 2024 to the primary completion date, 1 Jul 2027
  • 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.

Prior treatment

  • Prior germline genetic testing with a 40+ multi-gene panel AND/OR prior somatic tissue (250+ gene) testing utilizing the tissue from the bronchoscopy or surgical resection

Other

  • Individuals who have situations that would limit compliance with the study requirements
  • Institutionalized (i.e. federal medical prison)
  • Pregnant

Who the study is looking for

  • Subject age 18 years and older
  • Subject is scheduled/was scheduled for a bronchoscopy or surgical resection as part of standard of care
  • Subject with a moderate to high risk of lung cancer based on clinical demographic and radiologic information or with suspected metastatic disease
  • Ability to provide blood or saliva sample
  • Ability to provide archived tissue
  • Subject is able to understand and adhere to study requirements and able to provide informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.