100 Participants Needed

Molecular Analysis for Lung Cancer

Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Mayo Clinic
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to evaluate the effectiveness of robotic biopsies in identifying genetic markers that may aid in diagnosing lung cancer. Researchers will collect blood or saliva samples, review medical records, and analyze any genetic variants found. The trial is suitable for individuals at moderate to high risk of lung cancer who are scheduled or were scheduled for a bronchoscopy. Participants must also provide a tissue sample from a past procedure.

As a Phase 2 trial, this research measures the treatment's effectiveness in an initial, smaller group, allowing participants to contribute to significant advancements in lung cancer diagnosis.

Why are researchers excited about this trial?

Researchers are excited about this trial because it aims to personalize lung cancer care through a more precise genetic approach. Unlike standard treatments that typically focus on generalized protocols like chemotherapy or radiation, this trial uses genomic counseling and testing to identify unique genetic variants in patients. By analyzing these specific genetic markers, the trial hopes to tailor treatments that better target the cancer's individual characteristics, potentially leading to more effective and personalized care options.

Who Is on the Research Team?

JS

Janani S. Reisenauer, M.D.

Principal Investigator

Mayo Clinic in Rochester

Are You a Good Fit for This Trial?

Inclusion Criteria

I am scheduled for a bronchoscopy as part of my treatment plan.
I am at moderate to high risk for lung cancer or might have cancer that has spread.
I can provide a blood or saliva sample.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Genomic Counseling and Testing

Participants receive genomic counseling and genomic testing education, undergo blood or saliva collection, provide previously collected tissue sample, and have medical records reviewed.

Up to 2 years

Follow-up

Participants are monitored for the adequacy of samples for sequencing and the development of a genomic data bank.

Up to 2 years

What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: ObservationalExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Mayo Clinic

Lead Sponsor

Trials
3,427
Recruited
3,221,000+